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    <title>Arteleo Chemistry Journal</title>
    <link>http://www.arteleo.com</link>
    <language>en-en</language>
    <pubDate>Tue, 21 Feb 2012 19:26:06 GMT</pubDate>

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 <title>Reactions of indole ProductChemistry</title>
 <description>Electrophilic aromatic substitution Electrophilic aromatic substitution of indole occurs on the five-membered pyrrole ring, because it is more reactive towards such reaction than a benzene ring. As an electron-rich heterocycle, indole undergoes electrophilic aromatic substitution primarily at C-3, for example bromination of indole. The Mannich reaction is another example of electrophilic aromatic substitution where indole can produce an aminomethyl derivative. Similarly, using the Vilsmeier...&lt;p&gt;&lt;a href="http://www.arteleo.com/product/reactions-of-indole.html"&gt;&lt;img src="http://www.arteleo.com/product/images/1270_129_226.jpg" style="width: 164pt; height: 47pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Tue, 21 Feb 2012 19:26:06 GMT</pubDate>
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 <title>Hydroformylation Organic Reactions 2</title>
 <description>Detlef Selent,a Klaus-Diether Wiese,b and Armin B rner3 aLeibniz-Institut f r Organische Katalyse, Buchbinderstr. 5-6, D-18055 bOxeno C-4 Chemie, Paul-Baumann-Str. 1, D-45772Marl Germany Bidentate phosphorus ligands bearing an O-acyl phosphite moiety show superior modifying properties to the rhodium catalyst used in the hydroformylation of internal olefins. Results obtained for the hydroformylation of internal octenes and 2-pentene, respectively, are presented. The new ligands do markedly...&lt;p&gt;&lt;a href="http://www.arteleo.com/organic-reactions-2/hydroformylation.html"&gt;&lt;img src="http://www.arteleo.com/organic-reactions-2/images/1242_148_319.jpg" style="width: 156pt; height: 189pt;" title="Figure SCHAKAL drawing [[ C3H5 acyi Pphosphite For distances Rh1 and angle see text Space group triclinic 382 219 817 1453 pcalcd 151 "/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">Figure SCHAKAL drawing [[ C3H5 acyi Pphosphite For distances Rh1 and angle see text Space group triclinic 382 219 817 1453 pcalcd 151 </media:description>
 <pubDate>Thu, 09 Feb 2012 13:12:50 GMT</pubDate>
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 <title>Conclusions Xes Organic Reactions 2</title>
 <description>The RPT of Pt Al2O3 catalysts improves the hydrogenation TOF and ee while sintering the Pt crystallites. The degree of TOF and ee enhancement induced by RPT increases with higher levels of reducible residues due to the poor performance of the initial catalyst. Pt sintering and potential residue retention also increase if higher reducible residue contents are present. Such catalysts tend to perform worse, even after RPT, than those with lower amounts of reducible residues. A cleaner catalyst...&lt;div class="feedflare"&gt;
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 <pubDate>Tue, 07 Feb 2012 16:32:11 GMT</pubDate>
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 <title>Pharmaceutical importance of aromatic compounds some examples ProductChemistry</title>
 <description>There are numerous examples of aromatic compounds that are pharmaceu-tically important as drugs or pharmaceutical additives. Just a few examples of pharmaceutically important aromatic compounds are cited here. Aspirin, a well known non-narcotic analgesic and antipyretic drug, is a classic example of a pharmaceutically important benzene derivative. Morphine, an aromatic alkaloid, is a narcotic habit-forming analgesic that is used extensively for the management of post-operative pain. Aromatic...&lt;p&gt;&lt;a href="http://www.arteleo.com/product/pharmaceutical-importance-of-aromatic-compounds-some-examples.html"&gt;&lt;img src="http://www.arteleo.com/product/images/1270_65_92.jpg" style="width: 55pt; height: 60pt;" title="Aspirin Acetyl salicylic acid"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">Aspirin Acetyl salicylic acid</media:description>
 <pubDate>Mon, 06 Feb 2012 11:43:36 GMT</pubDate>
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 <title>Limits of Detection Chromatography</title>
 <description>The limit of detection LOD of a system can be defined in two ways the concentration limit of detection CLOD and the mass limit of detection MLOD . The CLOD of a typical peptide is about 1 g mL using absorbance detection at 200 nm. If 10 nL are injected, this translates to an MLOD of 10 pg at three times the baseline noise. The MLOD illustrates the measuring capability of the instrument. The more important parameter is the CLOD, which relates to the sample itself. The CLOD for HPCE is relatively...&lt;div class="feedflare"&gt;
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&lt;/div&gt;</description>
 <category>Chromatography</category>
 <link>http://www.arteleo.com/chromatography/limits-of-detection.html</link>
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 <pubDate>Fri, 03 Feb 2012 21:32:18 GMT</pubDate>
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 <title>Rubber Catalyzed by IrCODpyPCyPF Organic Reactions 2</title>
 <description>Jianzhong Hu, Neil T. McManus, Garry L. Rempel Department of Chemical Engineering, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 The application of Ir COD PCy3 py PF6, COD 1,4 cyclooctadiene, PCy3 tricyclohexylphosphine, py pyridine Crabtree's catalyst 1 for the hydrogenation of nitrile butadiene rubber NBR has been investigated for the first time. The catalyst was efficient for selective hydrogenation of olefinic groups in NBR. A preliminary kinetic study was used to explore the...&lt;p&gt;&lt;a href="http://www.arteleo.com/organic-reactions-2/rubber-catalyzed-by-[ircodpypcypf.html"&gt;&lt;img src="http://www.arteleo.com/organic-reactions-2/images/1242_39_68.jpg" style="width: 232pt; height: 180pt;" title="Figure Effect [ two reaction pressures [RCN 172 130 "/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">Figure Effect [ two reaction pressures [RCN 172 130 </media:description>
 <pubDate>Tue, 31 Jan 2012 05:06:06 GMT</pubDate>
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 <title>Aromatics Organic Reactions 2</title>
 <description>Marta Catellani, Elena Motti, Sara Deledda, Fiorenza Faccini Dipartimento di Chimica Organica e Industriale dell'Universita, Parco Area delle Scienze, 17 A, 43100 Parma, Italy Alkylaromatic palladacycles, formed in situ by reaction of palladium acetate with a strained and rigid cycloolefin such as norbornene and an ortho-substituted aryl iodide, allow the selective arylation of the aromatic ring by a second molecule of aryl iodide with subsequent norbornene expulsion. Coupling the resulting...&lt;p&gt;&lt;a href="http://www.arteleo.com/organic-reactions-2/aromatics.html"&gt;&lt;img src="http://www.arteleo.com/organic-reactions-2/images/1242_145_303.png" style="width: 328pt; height: 393pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Mon, 30 Jan 2012 18:27:55 GMT</pubDate>
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 <title>Significance of stereoisomerism in determining drug action and toxicity ProductChemistry</title>
 <description>Pharmacy is a discipline of science that deals with various aspects of drugs. All drugs are chemical entities, and a great majority 30-50 per cent of them contain stereocentres, show stereoisomerism and exist as enantiomers. Moreover, the current trend in drug markets is a rapid increase of the sales of chiral drugs at the expense of the achiral ones. In the next few years, chiral drugs, whether enantiomerically pure or sold as a racemic mixture, will dominate drug markets. It is therefore...&lt;p&gt;&lt;a href="http://www.arteleo.com/product/significance-of-stereoisomerism-in-determining-drug-action-and-toxicity.html"&gt;&lt;img src="http://www.arteleo.com/product/images/1270_7_49.jpg" style="width: 197pt; height: 46pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Mon, 16 Jan 2012 14:07:44 GMT</pubDate>
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 <title>F Gls ChemicalProperties</title>
 <description>The sulfur atom in the sulfite ion, SO32 , can be described as sp3 hybridized. One of these hybrid orbitals contains the sulfur lone pair, and the remaining three overlap with oxygen orbitals to form bonds. AB3U molecules and ions, each having four regions of high electron density around the central atom, usually have tetrahedral electronic geometry, trigonal pyramidal molecular geometry, and sp3 hybridization on the central atom. We must remember that theory and its application depends on...&lt;div class="feedflare"&gt;
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 <category>ChemicalProperties</category>
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 <pubDate>Sat, 17 Dec 2011 21:15:25 GMT</pubDate>
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 <title>x chnvcchchnJcchchnJ DrugSynthesis</title>
 <description>Reaction of the Mannich product 112 from acetophenone itself with the Grignard reagent from p-chlorobenzyl chloride gives the carbinol, 113. Dehydration in this case gives the antihistamine pyrrobutamine 114 .29 It is not immediately clear why dehydration does not occur in the other sense so as to afford the energetically more favored stilbene. As a class, analgesics tend to be built around portions of the morphine molecule that, as a minimum, incorporate a piperi-dine ring. The detailed...&lt;p&gt;&lt;a href="http://www.arteleo.com/drug-synthesis/x-chnvcchchnjcchchnj.html"&gt;&lt;img src="http://www.arteleo.com/drug-synthesis/images/1712_57_155.png" style="width: 322pt; height: 217pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <category>DrugSynthesis</category>
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 <pubDate>Fri, 09 Dec 2011 13:34:57 GMT</pubDate>
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 <title>I Axu ChemicalProperties</title>
 <description>Step 2 N 2 X 8 for Cl 1 X 4 for Be 20 e- needed A 2 X 7 for Cl 1 X 2 for Be 16 e- available 5 N - A 20 e- - 16 e- 4 e- shared Step 3 Cl s Be s Cl Step 4 Cl Be Cl or Cl Be Cl Calculation of formal charges shows that for Be, FC 2 - 2 0 0 and for Cl, FC 7 - 1 6 0 Screen 9.7, Electron-Deficient Compounds. BF3 and BQ3 are gases at room temperature. Liquid BBr3 and solid BI3 are shown here. BF3 and BQ3 are gases at room temperature. Liquid BBr3 and solid BI3 are shown here. In BeCl2, the chlorine...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemical-properties/i-axu.html"&gt;&lt;img src="http://www.arteleo.com/chemical-properties/images/1385_2875_235.jpg" style="width: 144pt; height: 216pt;" title="BF3 and BQ3 are gases room temperature Liquid BBr3 and solid BI3 are shown here"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <category>ChemicalProperties</category>
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 <media:title />
 <media:description type="html">BF3 and BQ3 are gases room temperature Liquid BBr3 and solid BI3 are shown here</media:description>
 <pubDate>Fri, 25 Nov 2011 18:29:39 GMT</pubDate>
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 <title>chcc hnconh chcnhcnh DrugSynthesis</title>
 <description>It will be recalled that both epinephrine and norepinephrine are pressor agents, that is, they cause an increase in blood pressure. It would therefore be expected that antagonists to these endogenous pressor amines might have a useful effect on hypertension. One approach to this problem consists in the preparation of compounds that interfere with biosynthesis of these amines by the administration of false substrates that would be unable to go through the final steps of biogenesis. A crucial...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=SA2lYrnpwDo:JkRo7z91bZk:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=SA2lYrnpwDo:JkRo7z91bZk:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <category>DrugSynthesis</category>
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 <pubDate>Mon, 14 Nov 2011 12:23:00 GMT</pubDate>
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 <title>Limitations Of The Octet Rule For Lewis Formulas ChemicalProperties</title>
 <description>Recall that representative elements achieve noble gas electron configurations in most of their compounds. But when the octet rule is not applicable, the relationship S N A is not valid without modification. The following are general cases for which the procedure in Section 7-5 must be modified that is, there are four types of limitations of the octet rule. A. Most covalent compounds of beryllium, Be. Because Be contains only two valence shell electrons, it usually forms only two covalent bonds...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=AeD_DHi_GkY:1DZ5mftUBe0:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=AeD_DHi_GkY:1DZ5mftUBe0:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ChemicalProperties</category>
 <link>http://www.arteleo.com/chemical-properties/limitations-of-the-octet-rule-for-lewis-formulas.html</link>
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 <pubDate>Sat, 01 Oct 2011 16:06:01 GMT</pubDate>
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 <title>J Hat QuantumMechanics</title>
 <description>ck t 2 _ VkmVmk -e-i w mk t - ei w mk t 2 O V3 1 - I' ck t 2 _ 1 - I' VkmVmk -e-i w mk t - ei w mk t 2 O V3 1 I' VkmVmk e-i w mk t ei w mk t - 2 O V3 .'. to order V2, cm t 2 _ 1 - I' ck t 2, with no assumptions made regarding V For the adiabatic perturbation case ih2h Em - Ej il-h -ih2h Em - Ej - ihh&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=nL0dqQtse2Y:Q7FZfQbyHvo:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=nL0dqQtse2Y:Q7FZfQbyHvo:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>QuantumMechanics</category>
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 <pubDate>Fri, 23 Sep 2011 01:54:59 GMT</pubDate>
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 <title>Iii Stability And Toxicity Of Polyalkylcyanoacrylate Nanoparticles ColloidalBiomolecules</title>
 <description>Degradation and toxicity of poly alkylcyanoacrylates is often discussed in the literature especially for the in vivo applications of nanoparticles as drug delivery systems. Concerning the stability of the nanoparticles, different pathways for their degradation have been described. The predominent mechanism greatly depends on the experimental conditions. Among the known degradation pathways, the most likely to occur in vivo are of two kinds. One mechanism consists of hydrolysis of the ester bond...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=IeuaPt1I0YM:yVSSAodjvGY:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=IeuaPt1I0YM:yVSSAodjvGY:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ColloidalBiomolecules</category>
 <link>http://www.arteleo.com/colloidal-biomolecules/iii-stability-and-toxicity-of-polyalkylcyanoacrylate-nanoparticles.html</link>
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 <pubDate>Fri, 23 Sep 2011 00:58:27 GMT</pubDate>
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 <title>b Yzw Chemiluminescence</title>
 <description>Figure 14 a ECL intensity versus potential for 4.1 x 10-4 M 250 ppm Al HQS 32 and 0.05 M TPrA in aqueous solution 0.2M KH2PO4 . b A Photolumiminescence of 0.4 mM solution of Al HQS 3 slit widths 3 nm in 0.2 M KH2PO4 and B electrochemi-luminescence of 0.4 mM solution of Al HQS 3 slit widths 10 nm in 0.2 M KH2P04 0.05M TPrA. ECL spectrum offset by 100 nm to the red for clarity. Conditions for ECL emission were optimized with the ECL correlating to aluminum concentration over several orders of...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemiluminescence/b-yzw.html"&gt;&lt;img src="http://www.arteleo.com/chemiluminescence/images/1338_748_156.jpg" style="width: 319pt; height: 180pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=O6Ew0fVFtPU:xUSIYAVYXW4:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=O6Ew0fVFtPU:xUSIYAVYXW4:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>Chemiluminescence</category>
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 <pubDate>Fri, 23 Sep 2011 00:57:38 GMT</pubDate>
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 <title>Crystallization Kinetics And Nucleation Mechanisms In The Presence Of Melt Mesophases Block Copolymer Science</title>
 <description>Polymer crystallization proceeds by nucleation and growth for a recent review of homopolymer crystallization, including kinetics and mechanism, see Schultz 2001 . If the polymer is free of contaminants, homogeneous nucleation initiates crystallization. Homogeneous nucleation requires the formation of a critical nucleus the process is thermally activated and has a large energy barrier. A large undercooling is therefore expected for homogeneous nucleation to occur at a substantial rate. In...&lt;p&gt;&lt;a href="http://www.arteleo.com/block-copolymer-science/crystallization-kinetics-and-nucleation-mechanisms-in-the-presence-of-melt-mesophases.html"&gt;&lt;img src="http://www.arteleo.com/block-copolymer-science/images/1319_98_120.jpg" style="width: 334pt; height: 309pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=C5FWzJ5rqcM:ZHlAJQIFJ3w:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=C5FWzJ5rqcM:ZHlAJQIFJ3w:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
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 <pubDate>Fri, 23 Sep 2011 00:35:34 GMT</pubDate>
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 <title>Info Mvk Cosmetic Formulations 6</title>
 <description>1. Mix the Arlatone 2121 in the heated water phase at 80C under moderate stirring until a homogeneous dispersion is formed. 2. Disperse the hydrocolloid in the heated aqueous phase at 75C with moderate stirring. 3. Add the heated oil phase to the aqueous phase under intensive sti rri ng. 4. Homogenise the mixture intensively at 750 for one minute. 5. Add phases D and E at -40C. 6. Cool to 35C whilst stirring moderately. 7. Add heat-sensitive ingredients whilst stirring moderately. Comments...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=IZ_Zxrd5v9A:RadYO1qdqk0:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=IZ_Zxrd5v9A:RadYO1qdqk0:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Fri, 23 Sep 2011 00:31:09 GMT</pubDate>
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 <title>All Alchemy ComputationalChemistry</title>
 <description>Alchemy 2000 we tested Version 2.05 is a graphic interface for running molecular mechanics and semiempirical calculations. Calculations can be done with the built-in Tripos force field or by calling the MM3 or MOPAC programs, which are included with the package. Alchemy is designed by Tripos and sold by SciVision. Molecules can be built using a two-dimensional sketch mode and are then converted to three-dimensional geometries by the program. It is also possible to build molecules in the...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=lbB3BrtpDfA:CzGR_C67LqE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=lbB3BrtpDfA:CzGR_C67LqE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ComputationalChemistry</category>
 <link>http://www.arteleo.com/computational/all-alchemy.html</link>
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 <pubDate>Fri, 23 Sep 2011 00:27:15 GMT</pubDate>
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 <title>Info Mla ApproachingChemistry</title>
 <description>an evacuated chamber, where it is bombarded with a beam of high-energy electrons. The electron beam knocks other electrons from the sample molecules, which become positively charged ions. Some of these ionized molecules survive, and others fragment into smaller ions. The various ions of different masses are then accelerated by an electric field and passed between the poles of a strong magnet, which deflects them through a curved, evacuated pipe. The radius of deflection of a charged ion M as it...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemistry/info-mla.html"&gt;&lt;img src="http://www.arteleo.com/chemistry/images/1262_509_135.jpg" style="width: 272pt; height: 195pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=eZnTfZrqtQc:x6OWBCj5LBw:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=eZnTfZrqtQc:x6OWBCj5LBw:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ApproachingChemistry</category>
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 <pubDate>Fri, 23 Sep 2011 00:16:57 GMT</pubDate>
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 <title>Cas Rn 1 Chromatography</title>
 <description>Erucamide Ethyl palmitate Ethyl linoleate Ethyl oleate Ethyl stearate Ethanox 330 Hexadecane Hexacosane Hostanox O3 Hostavin TMN 20 Ionol 220 Ionox 100 Ionox 129 Ionox 220 Irgafos 168 Irgafos P-EPQ Irganox 245 Irganox 259 Irganox 565 Irganox 1010 Irganox 1035 Irganox 1076 Irganox 1098 Irganox 1222 Irganox 1330 Irganox 1425 Irganox 2246 Irganox 3052 FF Irganox 3114 Irganox MD1024 Irganox MD1025 Irganox PS800 Irganox PS802 Isonox 129 Kemamide U Lauric acid Lowinox 22M46 MHET Myristic acid Naugard...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=A2BJPvaU0EM:aYRmfhtd1rs:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=A2BJPvaU0EM:aYRmfhtd1rs:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>Chromatography</category>
 <link>http://www.arteleo.com/chromatography/cas-rn-1.html</link>
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 <pubDate>Thu, 22 Sep 2011 23:56:51 GMT</pubDate>
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 <title>Nickel Catalyst Organic Reactions 2</title>
 <description>Gregory J. Ward and Bryan C. Blanchard Solutia, Inc., P.O. Box 97, Gonzalez, FL 32560-0097 A process for the production of 3-dimethylaminopropylamine DMAPA in high gt 99 purity from N,N-dimethylaminopropionitrile DMAPN utilizing a low pressure slurry hydrogenation process is described. The basic process comprises contacting the nitrile with hydrogen at low pressure in the presence of a sponge nickel catalyst under conditions sufficient to effect the conversion of the nitrile to the primary...&lt;p&gt;&lt;a href="http://www.arteleo.com/organic-reactions-2/nickel-catalyst.html"&gt;&lt;img src="http://www.arteleo.com/organic-reactions-2/images/1242_13_26.png" style="width: 303pt; height: 210pt;" title="Figure Experimental apparatus"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=Ghou7Zo2kLc:bNl10I4pDEg:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=Ghou7Zo2kLc:bNl10I4pDEg:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <media:description type="html">Figure Experimental apparatus</media:description>
 <pubDate>Thu, 22 Sep 2011 22:43:05 GMT</pubDate>
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 <title>Mechanisms Of Corrosion Processes Electrochemistry</title>
 <description>The analysis of corrosion processes comprises examining the special features in a given metal's anodic dissolution, establishing the nature of the cathodic reaction which is coupled with metal dissolution , and defining in greater detail the loci of the anodic and cathodic partial reaction. In corrosion, the equilibrium potential of reduction of the oxidizing agent is always more positive than that of dissolution of the metal at the given solution composition . The main cathodic reactions in...&lt;p&gt;&lt;a href="http://www.arteleo.com/electrochemistry/mechanisms-of-corrosion-processes.html"&gt;&lt;img src="http://www.arteleo.com/electrochemistry/images/1380_933_159.png" style="width: 216pt; height: 145pt;" title="FIGURE Schematic polarization curves for spontaneous dissolution active metals passivated metals Anodic curves for active metals cathodic curve for hydrogen evolution cathodic curve for air oxygen reduction anodic curve the passivated metal"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=j7pn8ClTdro:FLLNo5e1lGo:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=j7pn8ClTdro:FLLNo5e1lGo:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <category>Electrochemistry</category>
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 <media:title />
 <media:description type="html">FIGURE Schematic polarization curves for spontaneous dissolution active metals passivated metals Anodic curves for active metals cathodic curve for hydrogen evolution cathodic curve for air oxygen reduction anodic curve the passivated metal</media:description>
 <pubDate>Thu, 22 Sep 2011 22:40:56 GMT</pubDate>
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 <title>L R Subramanian DienesPolyenes</title>
 <description>Institut fur Organische Chemie, Technical University of Braunschweig, Hagenring 30, D-38106 Braunschweig, Germany Department of Chemistry, University of Warsaw, Pasteura Str. 1, 02-083 Poland Research Institute for Science and Technology, Kin-Ki University, Higashi-Osaka 577, Japan Casali Institute of Applied Chemistry, The Hebrew University of Jerusalem, Givat Ram Campus, Jerusalem 91904, Israel Department of Chemistry, University of California, Berkeley, California 94720-1460, USA Tottori...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=cl_ng71ShE4:v6qNKkjGATQ:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=cl_ng71ShE4:v6qNKkjGATQ:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
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 <pubDate>Thu, 22 Sep 2011 22:37:29 GMT</pubDate>
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 <title>Casting Xx Alloys Containing Magnesium And Manganese Aluminum</title>
 <description>Casting alloys of the A1 Mg-Si system are discussed in Chapter 2, here we only consider the effect of Mn on solidification paths in A356.0-type alloys. The main implication of Mn on the sequence of solidification in this type of alloys is the occurrence of two eutectic reactions with the formation of the Al15 FeMn 3Si2 phase. The amount of this phase is larger at higher cooling rates. Backerud et al. 1990 suggested schematic solidification paths that are relevant to A356-type alloys with and...&lt;p&gt;&lt;a href="http://www.arteleo.com/aluminum/casting-xx-alloys-containing-magnesium-and-manganese.html"&gt;&lt;img src="http://www.arteleo.com/aluminum/images/1540_2458_135.png" style="width: 222pt; height: 146pt;" title="Figure Diagrams solidification paths for two A356 type alloys containing and and after Backerud 1990 Numbers lines correspond solidification reactions Table "/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=PwEGLmlW8u8:GGzU45SiiGE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=PwEGLmlW8u8:GGzU45SiiGE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>Aluminum</category>
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 <media:title />
 <media:description type="html">Figure Diagrams solidification paths for two A356 type alloys containing and and after Backerud 1990 Numbers lines correspond solidification reactions Table </media:description>
 <pubDate>Thu, 22 Sep 2011 22:17:01 GMT</pubDate>
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 <title>Info Jqy ChemicalBonding</title>
 <description>To date, there are only a few 'first principles' estimates of and their effects on surface dynamics. One well-known example is the vibrational damping of molecules adsorbed on surfaces, where adiabatic theory cannot account for the short lifetimes large linewidths of adsorbed species 74 . Calculations of -qXX for C0 Cu 100 73,75,76 and on other surfaces 77 are in good agreement with lifetimes linewidths observed in experiments. Low-dimensional MDEF with ab initio Vxx 68 suggest that the...&lt;p&gt;&lt;a href="http://www.arteleo.com/bonding/info-jqy.html"&gt;&lt;img src="http://www.arteleo.com/bonding/images/1246_349_108.jpg" style="width: 177pt; height: 140pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;</description>
 <category>ChemicalBonding</category>
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 <pubDate>Thu, 22 Sep 2011 21:38:54 GMT</pubDate>
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 <title>Polysaccharides BiodegradablePolymers</title>
 <description>Starch is a polymer of D-glucose organised in two major constituents of huge molecular weights amylose and amylopectin. Amylose contains amorphous and crystalline regions. It forms a linear structure constituted by repeating units of 1-4a-glucose Fig. 1.1 . Amylopectin is branched on amylose in starch Fig. 1.2 Moore and Saunders, 1997 Flieger et al., 2003 . The natural crystalline structure of starch must be dismantled in order to produce a thermoplastic material. It is achieved by the...&lt;p&gt;&lt;a href="http://www.arteleo.com/biodegradable-polymers/polysaccharides.html"&gt;&lt;img src="http://www.arteleo.com/biodegradable-polymers/images/1238_26_5.jpg" style="width: 323pt; height: 109pt;" title=" Structure main subunits lignin"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html"> Structure main subunits lignin</media:description>
 <pubDate>Thu, 22 Sep 2011 21:26:30 GMT</pubDate>
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 <title>References Uvf BiodegradablePolymers</title>
 <description>Babanalbandi A, Hill D J T, Hunter D S, Kettle L 1999 , 'Thermal stability of poly lactic acid before and after y-radiolysis', Polym. Int., 48 10 , 980-984. Baiardo M, Frisoni G, Scandola M, Rimelen M, Lips D, Ruffieux K, Wintermantal E 2003 , 'Thermal and mechanical properties of plasticized poly L-lactic acid ', J. Appl. Polym. Sei., 90, 1731-1738. Berl M, Scharngal N 1988 , 'Poly lactones 9. Polymerization mechanism of metal alkoxide initiated polymerizations of lactide and various...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 20:54:37 GMT</pubDate>
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 <title>Vibrational normal coordinates Computational Chemistry 3</title>
 <description>The potential energy is approximated by a second-order Taylor expansion around the stationary geometry x0. V x V xo x - xo 2 x - xo t IdV - Xo 1637 The energy for the expansion point, V x0 , may be chosen as zero, and the first derivative is zero since x0 is a stationary point. Here F is a 3Natom x 3Natom force constant matrix containing the second derivatives of the energy with respect to the coordinates. The nuclear Schr dinger equation for an Natom system is given by eq. 16.39 . Eq. 16.39 is...&lt;p&gt;&lt;a href="http://www.arteleo.com/computational-3/vibrational-normal-coordinates.html"&gt;&lt;img src="http://www.arteleo.com/computational-3/images/1473_3735_171.jpg" style="width: 153pt; height: 35pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 20:30:01 GMT</pubDate>
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 <title>II SAMPLE PREPARATION Jfb ChromatographicAnalysis</title>
 <description>There are basically two methods used for the analysis of A -nitrosamines in water samples. Those are liquid-liquid extraction using an organic solvent, and adsorption onto a sorbent material. The most popular solvent is the dichloromethane DCM for two reasons the volatile nitrosamines are highly soluble in this solvent, and the boiling point of the DCM is low, hence preventing the volatilization or the degradation of nitrosamines through a subsequent concentration step. In this extraction...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 20:06:48 GMT</pubDate>
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 <title>OH Bbi Carbohydrates</title>
 <description>3,4-Ditosyl, di-Me acetal 2,5-Anhydro-3,4-di-O-tosyl-D-lyxose dimethyl acetal Mp 139-140 . a r gt 63.5 CHCl3 . 3,4-Ditosyl, di-Me acetal 2,5-Anhydro-3,4-di-O-tosyl-L-lyxose dimethyl acetal Mp 139-140 . a D -58.5 c, 1.3 in CHCl3 . Defaye, J. et al., Carbohydr. Res., 1971, 20, 305 1,6-Anhydro-4-O- a-D-glucopyranosyl - -D-glucopyranose. Maltosan 6983-27-3&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 20:02:50 GMT</pubDate>
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 <title>How to Measure SF Chromatography</title>
 <description>Figure 1 indicates the principle of use of any CCC device for the equilibrium of two liquid, nonmiscible phases. In this case, the stationary phase which is chosen is the lighter phase of the solvent system dark gray in Fig. 1 , whereas the mobile phase is indicated in white. For simplification, the coil is considered as an empty cylinder and the phenomena which occur inside the column are highly schematized as a stack of disks of mobile and stationary phases. This allows us to visualize the...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 19:58:17 GMT</pubDate>
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 <title>Amines with aromatic ring FlavorChemistry</title>
 <description>P-14 P15 PI 6 PI 7 P.14 P.14 Benzenamine, aniline, phenylamine, benzenamine, phenylazane, aminobenzene 62-53-3 Identified in green coffee by Vitzthum et al. 1976 . In their study on the influence of brewing time on the composition of brewed coffee, Lee et al. 1992 qualified aniline of 'fast extractor' 70-80 extracted after 5 min . When absolutely pure, in suitable dilution, aniline has a warm, sweet and actually pleasant odor Arctander, 1967 . P.15 Benzenamine, A -methyl-, N-methylaniline...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 19:57:03 GMT</pubDate>
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 <title>Aromatic sulfides FlavorChemistry</title>
 <description>Q.25 Benzene, methylthio -, methylsulfanyl benzene, methylthio benzene, methyl phenyl sulfide, thioanisole 100-68-5 FEMA 3873 Identified in roasted coffee flavor by Stoll et al. 1967 . At a concentration of 0.1 ppm it has a phenolic, quinoline, dirty flavor Chemisis, 1997 . Q.26 Phenol, 2- methylthio -, 2- methylsulfanyl phenol, 2- methylthio phenol, 2- methylmercapto phenol, o-hydroxythioanisole 1073-29-6J FEMA 3210 Identified by Stoll et al. 1967 . The flavor is described as burnt, phenolic,...&lt;div class="feedflare"&gt;
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 <category>FlavorChemistry</category>
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 <pubDate>Thu, 22 Sep 2011 19:57:03 GMT</pubDate>
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<item>
 <title>References Yyd Polysaccharides</title>
 <description>1. Chanzy H 1980 J Polym Sci, Polym Phys Ed 18 1137 2. Chanzy H, Nawrot S, Peguy A, Smith P 1982 J Polymer Sci 20 1909 3. Marini I, Brauneis F 1996 Textilveredelung 31 182 4. Firgo H, Eibl M, Eichinger D 1995 Lenzinger Ber 75 47 5. Brandner A, Zengel HG 1980 German Patent DE-OS 3,034,685 Chem Abstr 97 7727d CA 6. Ringel C 1969 Z Chem 9 188 7. Buijtenhuis FA, Abbas M, Witteveen AJ 1986 Papier 40 615 8. Rosenau T, Potthast A, Sixta H, Kosma P 2001 Progr Polym Sci 26 1763 9. Rosenau T, Potthast A,...&lt;div class="feedflare"&gt;
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&lt;/div&gt;</description>
 <category>Polysaccharides</category>
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 <pubDate>Thu, 22 Sep 2011 19:48:39 GMT</pubDate>
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 <title>References DegradationMethods</title>
 <description>1. Glaze WH, Kang JW, Chapin DH. The chemistry of water of water treatment processes involving ozone, hydrogen peroxide and ultraviolet radiation. Ozone Sci Eng 1987 9 335-342. 2. Sayre JM. International standards for drinking water. J Am Water Works Assoc 1988 80 53-60. 3. Organisation Mondiale de la Santee. Directives de qualitee pour l'eau de boisson. Vol. 1. Recommandations. Geneve Organization Mondiale de la Sante, 1994. 4. Rowe DR, Abdel-Magid IM. Handbook of wastewater reclamation and...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 19:35:53 GMT</pubDate>
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 <title>PolyEthylene GlycolAlkyl Dextran Ether DexPEGiCn for Drug Delivery Polysaccharides</title>
 <description>Amphiphilic poly ethylene glycol -alkyl dextran ethers are emerging as vehicles in the oral delivery of poorly water soluble drugs 251, 268, 269 . They form polymer micelles of low critical association concentrations CAC and small micelle sizes in aqueous solution. Particulate delivery systems lead to an enhancement of the absorption efficiency and bioavailability of highly lipophilic drugs orally applied, and provide the drug with some level of pro tection against degradation within the GI...&lt;p&gt;&lt;a href="http://www.arteleo.com/polysaccharides/polyethylene-glycolalkyl-dextran-ether-dexpegicn-for-drug-delivery.html"&gt;&lt;img src="http://www.arteleo.com/polysaccharides/images/1615_300_197.jpg" style="width: 330pt; height: 50pt;" title="Fig Synthesis poly ethylene glycol cetyl and stearyl dextran ether"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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&lt;/div&gt;</description>
 <category>Polysaccharides</category>
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 <media:description type="html">Fig Synthesis poly ethylene glycol cetyl and stearyl dextran ether</media:description>
 <pubDate>Thu, 22 Sep 2011 19:25:16 GMT</pubDate>
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 <title>References DiamondElectrochemistry</title>
 <description>1. M. Iwaki, S. Sato, K. Takahashi and H. Sakairi, Nucl. Instrum. Methods Phys. Res., 209 1983 1129. 2. Y. V. Pleskov, A. Ya. Sakharova, M. Krotova, L. L. Bouilov and B. V. Spitsyn, J. Electroanal. Chem., 228 1987 19. 3. K. Patel, K. Hashimoto and A. Fujishima, Denki Kagaku, 60 1992 659. 4. L. Boonma, T. Yano, D. A. Tryk, K. Hashimoto and A. Fujishima, J. Electrochem. Soc, 144 1997 L142. 5. T. N. Rao, D. A. Tryk, K. Hashimoto and A. Fujishima, J. Electrochem. Soc., 146 1999 680. 6. R. Tenne, K....&lt;div class="feedflare"&gt;
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 <category>DiamondElectrochemistry</category>
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 <pubDate>Thu, 22 Sep 2011 19:25:00 GMT</pubDate>
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 <title>References Wgq DiamondElectrochemistry</title>
 <description>1. M.E. Johll, D.G. Williams and D.C. Johnson, Electroanalysis, 9 1997 1397. 2. D.G. Davis and E. Bianco, Analyst Cambridge, UK , 119 1994 309. 3. R. Guidelli, F. Pergola and G. Rossi, Anal. Chem., 44 1972 745. 4. N.L. Weinberg and H.R. Weinberg, Chem. Rev., 68 1968 449. 5. I.H. Yeo and D.C. Johnson, J. Electroanal. Chem., 495 2001 110. 6. D.T. Fagan, I.F. Hu and T. Kuwana, Anal. Chem., 57 1985 2759. 7. J.W. Strojek, M.C. Granger, T. Dallas, M.W. Holtz and G.M. Swain, Anal. Chem., 68 1996 2031....&lt;div class="feedflare"&gt;
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 <category>DiamondElectrochemistry</category>
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 <pubDate>Thu, 22 Sep 2011 19:16:23 GMT</pubDate>
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 <title>NearMegahertz Sonochemistry DegradationMethods</title>
 <description>In the past, it was argued that 20-50 kHz was the optimal frequency range for sonochemistry 1,33 . More recently, however, a large number of experiments have shown that this is often not the case. Generally, sonochemistry progresses as well, if not better, at the near-megahertz frequencies i.e., 1001000 kHz see Sec. II.C.1 . It is expected that near-megahertz ultrasonic frequencies will soon become as important to sonochemistry as 20-50 kHz has been in the past. Generally, higher-frequency...&lt;p&gt;&lt;a href="http://www.arteleo.com/degradation-methods/nearmegahertz-sonochemistry.html"&gt;&lt;img src="http://www.arteleo.com/degradation-methods/images/1248_124_61.jpg" style="width: 360pt; height: 16pt;" title="Figure Beam geometry linear ultrasound"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 18:42:33 GMT</pubDate>
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 <title>E V vs AgAgCI satd KCI Nanotechnology 3</title>
 <description>FIGURE 14.6. Cyclic voltammetric curves for a Au81Pt19 C catalyst 24 wt. on GC electrode 0.07 cm2 in 0.5M H2SO4 electrolytes saturated with O2 solid curves and Ar dash curves . Scan rate 50 mV s from Ref. 35 . TABLE 14.1. Electrocatalytic activities of several different catalysts for ORR saturated O2 in terms of peak potential Epa and peak current pa from Ref. 35 .&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=TXAGCkeG19o:rnI5lkYyqVY:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=TXAGCkeG19o:rnI5lkYyqVY:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 18:35:26 GMT</pubDate>
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 <title>Coordination Polymerization PollutionControl</title>
 <description>Until 1953 there were only three mainline methods in common use for the initiation or catalysis of the polymerization of vinylic monomers. These were based on free radical, cationic, and anionic techniques. However, in that year Karl Ziegler, working in Germany, announced his discovery that ethylene could be polymerized to a high molecular weight, easily crystallized product under relatively mild conditions. The key to this success lay in the preparation of a heterogeneous catalyst from...&lt;p&gt;&lt;a href="http://www.arteleo.com/pollution-control/coordination-polymerization.html"&gt;&lt;img src="http://www.arteleo.com/pollution-control/images/1403_5010_250.png" style="width: 334pt; height: 234pt;" title="Bridging with new monomer FIGURE bimetallic mechanism for coordination Ziegler Natta polymerization"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=-s-WpJxVUvU:F5-YNYLLnjE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=-s-WpJxVUvU:F5-YNYLLnjE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <media:description type="html">Bridging with new monomer FIGURE bimetallic mechanism for coordination Ziegler Natta polymerization</media:description>
 <pubDate>Thu, 22 Sep 2011 18:25:44 GMT</pubDate>
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 <title>Ohccho HeterocyclicCompounds</title>
 <description>Formation of Pyrazino 1,2,3-de quinoxalines 194 gave 5-phenyl-2,3-dihydro-1H, 195 COCl 2, Et3N 30 880 also analogs.880,1080 Formation of Pyrazino 2,3-g quinazolines Ethyl 196 and urea gave 3H -dione 197 neat reactants, 198 C, 20 min 92 analogs likewise.&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=BfR1hMi0eSA:EiibMBid89Q:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=BfR1hMi0eSA:EiibMBid89Q:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 17:45:12 GMT</pubDate>
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 <title>List of contributors Fire Retardant Materials</title>
 <description>Dean, Faculty of Technology Bolton Institute Deane Road Bolton BL3 5AB UK Tel 01204 903831 Fax 01204 381107 E-mail arh1 bolton.ac.uk Tel 0161 295 4262 Fax 0161 295 5222 E-mail d.price salford.ac.uk Professor D Price, Fire Chemistry Research Group, School of Sciences, University of Salford, Salford, Manchester M5 4WT, UK Dr Geoff Anthony, Great Lakes Chemicals Tenax Road, Trafford Park, Manchester M17 1WT, UK Dr P Carty, Department of Chemical and Life Sciences, University of Northumbria at...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=TWRAzIlsPOQ:L1p0qt2kybE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=TWRAzIlsPOQ:L1p0qt2kybE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 17:17:46 GMT</pubDate>
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 <title>Preface For Chemical Reaction Chemical Reaction Dynamics</title>
 <description>Chemical reaction dynamics research has been an important field in physical chemistry and chemical physics research during the last few decades. This field of research has provided crucial support for atmospheric chemistry, interstellar chemistry as well as combustion chemistry. The development in this field has also greatly enhanced our understanding of the nature of bimolecular and unimolecular chemical reactions, and intermolecular and intramolecular energy transfer processes. Even though...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 17:12:38 GMT</pubDate>
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 <title>books on heterogeneous catalysis of organic reactions HeterogeneousCatalysis</title>
 <description>Not many books specifically address heterogeneous catalysis of organic reactions. The following list includes those whose aim is practical organic synthesis using heterogeneous catalysts and or the fine chemicals industry One, Stereochemistry of Heterogeneous Metal Catalysis, by M. Bartok and his faculty at The Department of Organic Chemistry at Jozsef Attila University in Szeged, Hungary, includes discussions of reaction mechanisms in many chapters. And the most recent addition, Heterogeneous...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=iUKlvA_suYM:qNXamBQeMqY:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=iUKlvA_suYM:qNXamBQeMqY:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 17:12:05 GMT</pubDate>
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 <title>Siemens Automotive SA Siemens AG CatalyticConverters</title>
 <description>The method of W09309335 1993 and US5487269 1996 is applied for the layout of fig. 76 and is explained with the help of fig. 77. Fig 76 shows an internal combustion engine equipped with an air filter, an air inlet duct and a throttle valve for regulating the inlet air flow rate, downstream of which there is an inlet pressure sensor which supplies a signal to a computer CPU . A sensor for the speed of the engine, fixed facing a flywheel of this engine, supplied a second signal to the computer....&lt;p&gt;&lt;a href="http://www.arteleo.com/catalytic-converters/siemens-automotive-sa-siemens-ag.html"&gt;&lt;img src="http://www.arteleo.com/catalytic-converters/images/1515_53_86.jpg" style="width: 268pt; height: 125pt;" title="Fig from W09309335"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=d1rIrkFcOJM:y0SJD2jfHEo:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=d1rIrkFcOJM:y0SJD2jfHEo:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>CatalyticConverters</category>
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 <media:title />
 <media:description type="html">Fig from W09309335</media:description>
 <pubDate>Thu, 22 Sep 2011 17:11:29 GMT</pubDate>
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 <title>Automated Macrosorting Systems PlasticsTechnologies</title>
 <description>Much macrosorting, such as separating PET bottles from HDPE bottles, nylon carpet from polyester carpet, and so on, is still done by hand, often by workers picking materials off conveyor belts and placing them in the appropriate receptacle. However, mechanized means of sorting to make the process more economical and reliable continue to become more prevalent. The various devices commercially available to separate plastics by resin type typically rely on differences in the absorption or...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=8ySROwbtm-o:_tHy4h1r9fg:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=8ySROwbtm-o:_tHy4h1r9fg:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>PlasticsTechnologies</category>
 <link>http://www.arteleo.com/plastics-technologies/automated-macrosorting-systems.html</link>
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 <pubDate>Thu, 22 Sep 2011 16:55:42 GMT</pubDate>
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 <title>Practical Chiral Detectors ChromatographicDetectors</title>
 <description>There are two basic types of chiral detectors for LC, those that measure optical rotation and those that measure circular dichroism. At the time of writing this book, the only commercially available chiral detectors are those that measure optical rotation. Nevertheless, a detector that measures circular dichroism and utilizes a diode array sensor system is thought to be in the design stage and will be briefly described later. The successful development of a chiral detector based on optical...&lt;p&gt;&lt;a href="http://www.arteleo.com/chromatographic-detectors/practical-chiral-detectors.html"&gt;&lt;img src="http://www.arteleo.com/chromatographic-detectors/images/1280_108_201.jpg" style="width: 292pt; height: 310pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=NVEQApi-slE:8kM2PEkZo90:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=NVEQApi-slE:8kM2PEkZo90:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ChromatographicDetectors</category>
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 <pubDate>Thu, 22 Sep 2011 16:32:25 GMT</pubDate>
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 <title>Types Of Polymers And Polymerizations Polymerization</title>
 <description>There has been and still is considerable confusion concerning the classification of polymers. This is especially the case for the beginning student who must appreciate that there is no single generally accepted classification that is unambiguous. During the development of polymer science, two types of classifications have come into use. One classification is based on polymer structure and divides polymers into condensation and addition polymers. The other classification is based on...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=uTM8HQ66PyQ:S93QYVQYdKE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=uTM8HQ66PyQ:S93QYVQYdKE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>Polymerization</category>
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 <pubDate>Thu, 22 Sep 2011 16:00:14 GMT</pubDate>
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 <title>Joule Heating CapillaryElectrophoresis</title>
 <description>The conduction of electric current through an electrolytic solution generates heat via frictional collisions between migrating ions and buffer molecules. Since high field strengths are employed in HPCE, ohmic or Joule heating can be substantial. There are two problems that can result from Joule heating 1. Temperature changes due to ineffective heat dissipation 2. Development of thermal gradients across the capillary If heat is not dissipated at a rate equal to its production, the temperature...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=E31AQVHfMtY:-swdOS-v194:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=E31AQVHfMtY:-swdOS-v194:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <category>CapillaryElectrophoresis</category>
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 <pubDate>Thu, 22 Sep 2011 15:58:52 GMT</pubDate>
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 <title>CH Wfy AsymmetricSynthesis</title>
 <description>5.1.3 Chiral s-Unsubstituted N-Acyloxazolidinones Chiral a, -unsaturated -acyloxazolidinones have been regarded as a complement for type I dienophile reagents. Evans et al.4 reported a Diels-Alder reaction promoted by dialkyl aluminum chloride. In this reaction, chiral a, -unsaturated -acyloxazolidinones were used as highly reactive and diaster-eoselective dienophiles. The stereogenic outcome of the Diels-Alder adducts 34 and 36 depends on the chirality at C-4 of the oxazolidinone auxiliaries....&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 15:58:35 GMT</pubDate>
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 <title>Our Daily Lives ChemicalProperties</title>
 <description>Y ou may have encountered some salts of ternary acids without even being aware of them. For example, the iron in many of your breakfast cereals and breads may have been added in the form of iron II sulfate, FeSO4, or iron II phosphate, Fe3 PO4 2 the calcium in these foods often comes from the addition of calcium carbonate, CaCO3. Fruits and vegetables keep fresh longer after an application of sodium sulfite, Na2SO3, and sodium hydrogen sulfite, NaHSO3. Restaurants also use these two sulfites to...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemical-properties/our-daily-lives.html"&gt;&lt;img src="http://www.arteleo.com/chemical-properties/images/1385_3618_344.jpg" style="width: 91pt; height: 87pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=1Jlpgg6voWc:FUGNGNxJRNs:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=1Jlpgg6voWc:FUGNGNxJRNs:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ChemicalProperties</category>
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 <pubDate>Thu, 22 Sep 2011 15:58:14 GMT</pubDate>
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 <title>Info Tsl AnalyticChemistry</title>
 <description>h 0.762 abs units, ta 14.1 s, T 15.8 s, t 1.7 s, At 15.2 s, T' 13.5 s, sensitivity 7.62 x 10-3 ppm-1, about 260-270 samples h 13,700 ppm Cl-0.071 M HCl a 2.52 b 68 samples h c 94.8 w w cocaine 6.27 x 10-4 M H2SO4&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=B09oH04UNZc:8r6l4IIDwvE:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=B09oH04UNZc:8r6l4IIDwvE:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>AnalyticChemistry</category>
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 <pubDate>Thu, 22 Sep 2011 15:58:00 GMT</pubDate>
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 <title>SCHEME Qea ChiralChemicals</title>
 <description>Although pig liver esterase PLE catalyzes the hydrolysis of all amino esters tested in this work, it was only enantioselective toward esters 30 R1 ArCH2, or n-Bu, R2 Et . This lack of correlation between enantioselectivity and substrate structure has been reported for many PLE catalyzed reactions.120121 The lipase CE was obtained as a crude extract containing about 10 of total protein. The active enzyme catalyzing the amino ester hydrolysis was isolated from the mixture and partially purified....&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=vV3Nk8prYks:u0ahC4doA90:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=vV3Nk8prYks:u0ahC4doA90:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
&lt;/div&gt;</description>
 <category>ChiralChemicals</category>
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 <pubDate>Thu, 22 Sep 2011 15:54:14 GMT</pubDate>
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 <title>H Qea ChemicalProperties</title>
 <description>No hydrogen atoms are attached to the carbon atoms that are involved in fusion of aromatic rings, that is, carbon atoms that are members of two or more aromatic rings. The traditional name is often used as part of the base name in naming an aromatic hydrocarbon and its derivatives. You should know the names and structures of the aromatic hydrocarbons discussed thus far benzene, toluene, the three xylenes, naphthalene, anthracene, and phenanthrene. Distillation of coal tar provides four volatile...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemical-properties/h-qea.html"&gt;&lt;img src="http://www.arteleo.com/chemical-properties/images/1385_8655_986.jpg" style="width: 481pt; height: 211pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 15:54:08 GMT</pubDate>
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 <title>Conclusion Fire Retardant Materials</title>
 <description>Polymer-layered silicate nanocomposites may be considered to be environmentally friendly alternatives to some traditional flame retardants. Not only does this fact give rise to a promising means of producing flame-retarding polymers, but it does not have the usual drawbacks associated with other additives. For instance, relatively low concentrations of silicates are necessary compared with the amounts used for conventional additive flame retardants in order to achieve similar or indeed,...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 15:52:46 GMT</pubDate>
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 <title>References 1 Ethanol</title>
 <description>Ackerson, M. D. 1991 , 16th IGT Conf Energy from Biomass and Wastes, Washington, DC, 725. Adt, R. R., Rhee, K. T. 1978 , U. S. Department of Energy, Report No. eY-76-5-05-5216, 8 pp. Agu, R. C, Amadife, A. E, Ude, C. M 1997 , Waste-Management. 17 1 , 91-96. Aiba, S., Shoda, M. 1969 , Ferment. Technol. 47,790. Aiba, S., Schoda, M., Natatani, M. 1968 , Biotechnol. Bioeng. 10,845. Alcon Biotechnology Ltd. 1980 , 20 Eastbourne Terrace, London. Anonymous 1978 , Chem. Eng. News 56 32 , 22. Anonymous...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 15:46:15 GMT</pubDate>
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 <title>Preparation of isoxazole pyrazole and isothiazole ProductChemistry</title>
 <description>Isoxazole and pyrazole synthesis While 1,3-diketones undergo condensation with hydroxylamine to produce isoxazoles, with hydrazine they yield corresponding pyrazoles. Isothiazole synthesis Isothiazole can be prepared from thioamide in the following way. Reactions of isoxazole, pyrazole and isothiazole Like 1,3-azoles, due to the presence of a pyridine-like nitrogen atom in the ring, 1,2-azoles are also much less reactive towards electrophilic substitutions than furan, pyrrole or thiophene....&lt;p&gt;&lt;a href="http://www.arteleo.com/product/preparation-of-isoxazole-pyrazole-and-isothiazole.html"&gt;&lt;img src="http://www.arteleo.com/product/images/1270_115_193.jpg" style="width: 220pt; height: 33pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:59:42 GMT</pubDate>
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 <title>C Vgf ChromatographicAnalysis</title>
 <description>Extrapolated response ' - Response - 5 Response Cm Minimum detectable concentration Cn Highest linear concentration FIGURE 4.1 A typical calibration curve peak area in absorbance units vs. concentration . Detector noise is the short-term noise in the maximum amplitude of response for all random variations of the detector signal of a frequency greater than one cycle per minute. Long term noise is similar to short term except that the frequency range is between 6 and 60 cycles per hour. Drift is...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:56:25 GMT</pubDate>
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 <title>O Ynm Carbohydrates</title>
 <description>Mp 82-83 . a D3 40.5 c, 1.0 in CHCl3 . 2,4-Dinitrophenylhydrazone Mp 180 . a D' 13.1 c, 0.4 in CHCl3 . 4-Ac C14H16O5 264.277 a D3 26.6 c, 1.0 in CHCl3 . Mp 95-96 . a D2 -23.1 c, 1.0 in CHCl3 . Collins, P.M. et al., Carbohydr. Res., 1974, 32, 203 Fischer, J.-C. et al., Can. J. Chem., 1977, 55, 4078&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:46:23 GMT</pubDate>
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 <title>Halide salts Corrosion of Aluminum</title>
 <description>Halide salts chlorides, fluorides, bromides, and iodides are generally more aggressive towards aluminium than sulphates and phosphates. Their aggressiveness decreases in the order given. 1 The term salt, used for these compounds since the 14th century, first by alchemists, stems from the analogy of their appearance and certain properties, such as their solubility in water, with salt NaCl. Oxidising salts such as chlorates, persulphates, nitrates, and perchlorates generally have no action,...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:35:00 GMT</pubDate>
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 <title>Time Reversal and Symmetry in the ManyElectron Hamiltonian QuantumChemistry</title>
 <description>We have seen how time-reversal symmetry and double-group symmetry are intimately connected in the matrices of one- and two-electron operators. These two symmetries are just as intimately connected in the many-electron Hamiltonian matrix. As for the one-electron matrices, we must choose a representation for the basis with which the matrices are represented. We take as our N-particle basis the determinant basis introduced in chapter 9, given in terms of A and B strings, and consider all possible...&lt;p&gt;&lt;a href="http://www.arteleo.com/quantum-chemistry/time-reversal-and-symmetry-in-the-manyelectron-hamiltonian.html"&gt;&lt;img src="http://www.arteleo.com/quantum-chemistry/images/1476_121_18.jpg" style="width: 190pt; height: 144pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:30:44 GMT</pubDate>
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 <title>Polyorthoesters BiodegradablePolymers</title>
 <description>These polymers appear to be particularly useful for controlled drug release. Initially poly orthoesters were prepared by condensation of 2,2-diethoxytetrahydrofuran and a dialcohol47 B ecause the tetrahydrofuran component of the polymers does not provide the necessary rigidity Tg varies from body temperature or lower , this material had limited utility as a solid implant designed for drug delivery. An alternative route uses 5,5 undecane and a dialcohol.48 Mechanical properties of the polymer...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:25:00 GMT</pubDate>
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 <title>Making Soda Pop From Alchemy to Chemistry</title>
 <description>Joseph Priestley 1733-1804 began a religious odyssey at an early age and is now recognized as one of the founders of Unitarianism.1'2 At 19 he entered the Dissenting Academy of Daventry to study for the Nonconformist Ministry, refecting the early influence of his aunt. By the age of 28 he taught languages including Hebrew , history, law, logic, and anatomy at the highly regarded Dissenting Academy at Warrington. His scientific interests were well under way by this time he had earlier purchased...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 14:19:25 GMT</pubDate>
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 <title>AreneMoCO Complexes TransitionMetal</title>
 <description>Arene tricarbonyl molybdenum complexes are yellow, often crystalline compounds. They are weakly air-sensitive in the solid state and have to be stored under inert atmosphere and out of light. They are best purified by crystallization. In solution, they are unstable to air. The trait that has most hampered development of the use of arene Mo CO 3 complexes in organic synthesis, however, is the lability of the arene metal bond. Lewis basic solvents such as THF, DMF, DM-SO, acetone and acetonitrile...&lt;p&gt;&lt;a href="http://www.arteleo.com/transition-metal/arenemoco-complexes.html"&gt;&lt;img src="http://www.arteleo.com/transition-metal/images/1739_9_6.jpg" style="width: 268pt; height: 194pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 13:51:42 GMT</pubDate>
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 <title>NNCarbonyldiimidazole CDI as Esterification Reagent Polysaccharides</title>
 <description>A method with an enormous potential for dextran modification is the homogeneous one-pot synthesis after in situ activation of the carboxylic acids with CDI, which is a rather well known technique in general organic chemistry and was published in 1962 197 . It is especially suitable for the functionalisation of the biopolymers, because during conversion the reactive imidazolide of the acid is generated and only CO2 and imidazole are formed as by-products Fig. 29 . The reagent and by-products are...&lt;p&gt;&lt;a href="http://www.arteleo.com/polysaccharides/nncarbonyldiimidazole-cdi-as-esterification-reagent.html"&gt;&lt;img src="http://www.arteleo.com/polysaccharides/images/1615_287_184.png" style="width: 269pt; height: 174pt;" title="Fig NMR spectroscopic investigation the situ activation acetic acid with CDI confirming complete consumption the CDI the acetyl imidazolide"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">Fig NMR spectroscopic investigation the situ activation acetic acid with CDI confirming complete consumption the CDI the acetyl imidazolide</media:description>
 <pubDate>Thu, 22 Sep 2011 13:46:06 GMT</pubDate>
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 <title>The Bucherer Reaction The Amino Group</title>
 <description>Naphthols and the corresponding naphthylamines are interconvertible in aqueous media containing sulphite or bisulphite ion at elevated temperatures23. Thus naphthols may be converted to naphthylamines by reaction with ammonia and ammonium sulphite in aqueous solution, usually in the temperature range 90-150 the corresponding dinaphthylamine is sometimes obtained as a byproduct reaction 15 . MonoaLkylamines and dialkylamines similarly give the alkylamino- and dialkylaminonaphthalenes, though...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 13:21:39 GMT</pubDate>
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 <title>Acidity of terminal alkynes ProductChemistry</title>
 <description>Terminal alkynes are acidic, and the end hydrogen can be removed as a proton by strong bases e.g. organolithiums, Grignard reagents and NaNH2 to form metal acetylides and alkynides. They are strong nucleophiles and bases, and are protonated in the presence of water and acids. Therefore, metal acetylides and alkynides must be protected from water and acids. CH3CH2Li _ - - RC C Li CH3CH3&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 13:20:15 GMT</pubDate>
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 <title>O Wag ChemicalProperties</title>
 <description>secondary amines. Amides contain the C N functional group. They are named as Most natural fatty acids contain even numbers of carbon atoms because they are synthesized in the body from two-carbon acetyl groups. Honeybees produce the wax to build their honeycombs. Figure 27-19 Models of long-chain fatty acids. The saturated fatty acids a are linear and tend to pack like sticks of wood to form solid masses in blood vessels, thereby constricting them. The trans unsaturated fatty acids have a...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemical-properties/o-wag.html"&gt;&lt;img src="http://www.arteleo.com/chemical-properties/images/1385_8935_1046.jpg" style="width: 145pt; height: 170pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 13:20:04 GMT</pubDate>
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 <title>PROBLEMS Nie Polymerization</title>
 <description>3-1 When one considers the various polymers produced from carbon-carbon double bond monomers, the following generalizations are apparent a. The polymers are produced almost exclusively from ethylene, monomers that have one substituent on the double bond, or monomers that have two substituents on the same carbon atom of the double bond. Monomers containing one substituent on each carbon of the double bond seldom polymerize. b. Most of the chain polymerizations are carried out by radical...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 13:11:02 GMT</pubDate>
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 <title>Master equations CondensedPhases</title>
 <description>As discussed in Section 8.1, a phenomenological stochastic evolution equation can be constructed by using a model to describe the relevant states of the system and the transition rates between them. For example, in the one-dimensional random walk problem discussed in Section 7.3 we have described the position of the walker by equally spaced points nAx n to, , to on the real axis. Denoting by P n, t the probability that the particle is at position n at time t and by kr and k the probabilities...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 12:59:38 GMT</pubDate>
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 <title>Dglycero Ltalo Heptonic acid dgulo Hexonolactone Carbohydrates</title>
 <description>D-glycero-l-talo -Heptonic acid, H-29 D-glycero-D-galacto -Heptono-1,4-lactone, H-23 D-glycero-D-gulo -Heptono-1,4-lactone, H-25 D-glycero-d-ido -Heptono-1,4-lactone, H-26 D-glycero-L-manno -Heptono-1,4-lactone, H-27 D-glycero-d-talo -Heptono-1,4-lactone, H-28 D-glycero- l-talo -Heptono-1,4-lactone, H-29 a-D-gluco -2-Heptulopyranosonic acid, H-64 Heptyl H-65 3- O -Heptyl-1,2- O -isopropylidene-a-d-glucofuranose, S-28 S-28 Herpid, D-278 Herplex, D-278 Hetangmycin, R-143 Hexa-O...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 12:47:41 GMT</pubDate>
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 <title>Mashing Processes Mashing Equipment Wet Cleaning of Potatoes Ethanol</title>
 <description>Before processing potatoes, they must be cleaned and free from sand, stones, soil, and potato foliage. For this purpose washing rolls with a minimum length of about 3 m and a minimum diameter of 1.5 m are used. The potatoes pass 0 1 2 3 4 5 6 24 48 72 96 Stillage Fermentation Time h Fig. 9. Saccharification of triticale mash using the enzyme combination OPTIMALT . Yeast added after 30 min of saccharification distillation after 96 h of fermentation. through the turning wash roll with...&lt;p&gt;&lt;a href="http://www.arteleo.com/ethanol/mashing-processes-mashing-equipment-wet-cleaning-of-potatoes.html"&gt;&lt;img src="http://www.arteleo.com/ethanol/images/1239_26_11.png" style="width: 250pt; height: 326pt;" title="Fig Henze cooker Kreipe 1981"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=olfOuEsXlE8:V-DV4J25tq8:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=olfOuEsXlE8:V-DV4J25tq8:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <media:description type="html">Fig Henze cooker Kreipe 1981</media:description>
 <pubDate>Thu, 22 Sep 2011 12:41:54 GMT</pubDate>
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 <title>H Bhl Pharmaceuticalsubstances</title>
 <description>DRP595 175 I. G. Farben 1931 . DRP590 175 I. G. Farben 1932 . Formulation s amp. 0.5g 5 g 10 as sodium salt D Dormopan Bayropharm -comb. wfm Evipan Bayer wfm Stodinox Lorenz -comb. wfm F Dormopan Bayer-Pharma -comb. wfm Noctivane Vaillant-Defresne wfm GB Evidorm Winthrop wfm J Cyclopan Teikoku Kagaku-Nagase Oltopan Dainippon Ouropan Soda Shionogi USA Sombulex Riker wfm rn 54-03-5 MF C H NAo MW 592.69 einecs 200-189-1 LD,0 34 mg kg r, i.v. cn 3,4,5-trimethoxybenzoic acid ester rn 50-62-4 MF CjoH...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 12:33:43 GMT</pubDate>
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 <title>Catalase Active Site Diagram IndustrialEnzymes</title>
 <description>J. Polaina and A.P. MacCabe eds. , Industrial Enzymes, 441-459. 2007 Springer. Figure 1. The reaction scheme for the oxidation of yS-D-glucose catalysed by glucose oxidase Figure 1. The reaction scheme for the oxidation of yS-D-glucose catalysed by glucose oxidase P. purpurogenum, P. variabile, P. chrysogenum and A. fumaricus are also good candidates for industrial applications Crueger and Crueger, 1990 Petruccioli et al., 1993 Leiter et al, 2004 . The A. niger and P. amagasakiense enzymes are...&lt;p&gt;&lt;a href="http://www.arteleo.com/industrial-enzymes/info-btg.html"&gt;&lt;img src="http://www.arteleo.com/industrial-enzymes/images/1447_1504_109.jpg" style="width: 327pt; height: 347pt;" title="Figure Proposed mechanism for galactose oxidation galactose oxidase according Whittaker 1988 represents the pyranose ring associated with galactose"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">Figure Proposed mechanism for galactose oxidation galactose oxidase according Whittaker 1988 represents the pyranose ring associated with galactose</media:description>
 <pubDate>Thu, 22 Sep 2011 12:32:27 GMT</pubDate>
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 <title>Our Daily Lives Wox ChemicalProperties</title>
 <description>A Spectacular View of One Mole of Electrons Early in our study of chemistry, we saw that atoms are made up of protons, neutrons, and electrons. We also discussed the incredibly large size of Avogadro's number, 6.022 X 1023. Although individual atoms and molecules are invisible to the naked eye, one mole of atoms or molecules is easily detected. Because subatomic particles are even smaller than atoms and also invisible, you might never expect to see individual electrons. Let's consider the...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemical-properties/our-daily-lives-wox.html"&gt;&lt;img src="http://www.arteleo.com/chemical-properties/images/1385_6953_750.jpg" style="width: 321pt; height: 180pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 12:19:12 GMT</pubDate>
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 <title>KIEs as Mechanistic Probes Biological Chemistry 2</title>
 <description>KIE measurements are routinely used for the elucidation of reaction mechanisms. The reaction coordinate represents the three-dimensional motion of all nuclei along the lowest-energy path that interconverts reactants and products. The reaction coordinate may represent the displacement of atoms within a chemical bond and or the reorientation of surrounding solvent molecules. Regardless of the nature of the reaction coordinate, isotope substitution does not change the electronic potential energy...&lt;p&gt;&lt;a href="http://www.arteleo.com/biological-2/kies-as-mechanistic-probes.html"&gt;&lt;img src="http://www.arteleo.com/biological-2/images/1347_380_276.jpg" style="width: 235pt; height: 238pt;" title="FIGURE Reaction coordinates for abstraction from methane depicting the transition state the intersection potential energy surfaces for stretching and bonds"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">FIGURE Reaction coordinates for abstraction from methane depicting the transition state the intersection potential energy surfaces for stretching and bonds</media:description>
 <pubDate>Thu, 22 Sep 2011 11:57:44 GMT</pubDate>
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 <title>Info Uub Physics and Chemistry 4</title>
 <description>Fig. 7. The influence of certain scattering or transport mechanisms on the contributions to thermal conductivity the symbol is given in the lower right corner of each rectangle in three temperature regions. Tc and Ts are the N cl, Curie and spin reorientation temperatures, respectively. Barbara et al. 1977 . Other compounds are ferromagnetics with Tc in the range 6168 K. The R atoms excluding Ce, Eu and Yb have valency 3. RA12 are metals. The measured k is equal to At temperatures T lt 0...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 11:29:01 GMT</pubDate>
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 <title>Info Kst Fire Retardant Materials</title>
 <description>The intercalated nanocomposites showed much higher char yields than any of the other polymer, immiscible and delaminated systems. The residual weights after different times at different temperatures from isothermal TGA experiments for PEI and PEI-intercalated nanocomposites are given in Table 6.1. There was, however, no difference between the montmorillonite- and fluorohectorite-based nanocomposites containing the same nanostructure, suggesting that the particle size of the silicates is not an...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 11:21:16 GMT</pubDate>
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 <title>Aluminous Goethite Clays</title>
 <description>It is considered as an ideal solid solution between the pure member FeOOH Y1 and the diaspore AlOOH Y2 FeY 1 A1Y2 00H with Y1 Y2 1. The amounts of Al3 and Fe3 depend on the local conditions imposed by the rock composition b FeY 1a1y2 OOH f FeZ1AlZ2 SiO2.5 OH 2 3.120 The equilibrium between Al-goethite and the solutions is reached when the partial equilibria with both composition end members is reached. Aluminous end member Y2 of goethite AlOOH c 3H aq Al aq 2 0 1 3.121 _ flAl3 X 42q log cai3 aH...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 11:15:27 GMT</pubDate>
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 <title>M References AnalyticChemistry</title>
 <description>1. Goedhart, M. J. Verdonk, A. H. J. Chem. Educ. 1991, 68, 1005-1009. 2. Rousseeuw, P. J. J. Chemom. 1991, 5, 1-20. 3. Ellison, S. Wegscheider, W. Williams, A. Anal. Chem. 1997, 69, 607A-613A. 4. Shoemaker, D. P. Garland, C. W. Nibler, J. W. Experiments in Physical Chemistry, 5th ed. McGraw-Hill New York, 1989, pp. 55-63. 5. Lam, R. B. Isenhour, T. L. Anal. Chem. 1980,52, 1158-1161. 6. Mark, H. Workman, J. Spectroscopy, 1988,3 1 , 44-48. 7. Winn, R. L. Statistics for Scientists and Engineers,...&lt;p&gt;&lt;a href="http://www.arteleo.com/analytic/m-references.html"&gt;&lt;img src="http://www.arteleo.com/analytic/images/1520_1004_66.jpg" style="width: 144pt; height: 94pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 11:00:06 GMT</pubDate>
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 <title>Info Gvf Cosmetic Formulations 5</title>
 <description>Heat the ingredients of fatty phase A to 70C. Heat the ingredients of water phase B to 75C. Under stirring add phase B to phase A , cool to 50C, homogenize and cool to 30C. Then add phase C and stir cold. SOURCE Pentapharm Ltd. Application No. G 006.A 03.96 A Imwitor 960K, Flakes Glyceryl Stearate SE 4.00 Mi glyol 840 Propylene Glycol Dicaprylate Dicaprate 7.00 Cetyl A1cohol 1.00 Hostaphat KL 340 N Di1aureth-4-Phosphate 5.00 B Preservative q.s. Keltrol F Gel 2 Xanthan Gum 30.00 Citric Aci d...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 10:57:27 GMT</pubDate>
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 <title>Info Tje Chromatography</title>
 <description>obtained from E. Merck India Ltd. Worli, Mumbai, India . Orthophosphoric acid and acetonitrile HPLC grade were obtained from Qualigens Fine Chemicals Dr. Annie Besant Road, Mumbai, India . The 0.45-p.m nylon filter was obtained from Advanced Microdevices Pvt. Ltd. Ambala Cantt, India and Whatman filter paper 41 was obtained from Whatman International Ltd. Maidstone, England, UK . The tablets containing a combination of metformin and glibenclamide were purchased from the Indian market....&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 10:36:45 GMT</pubDate>
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 <title>Comparison between TMB and SMB model Chromatography 3</title>
 <description>Concentration profiles of SMB models with three or more columns per section show good agreement with those of TMB models Ruthven et al., 1989, Lu and Ching, 1997 and Pais et al. 1998a . In this case, TMB models may be used to design SMB processes. Due to high investment costs SMB plants often have fewer columns. Therefore, SMB plant behavior differs considerably from the TMB process Chapter 7, Chu and Hashim, 1995, Strube et al., 1998a and Pais et al., 1998a . Anyhow, even today initial process...&lt;p&gt;&lt;a href="http://www.arteleo.com/chromatography-3/comparison-between-tmb-and-smb-model.html"&gt;&lt;img src="http://www.arteleo.com/chromatography-3/images/1624_2506_209.jpg" style="width: 325pt; height: 197pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 10:01:30 GMT</pubDate>
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 <title>Importance of functional groups in determining drug actions and toxicity ProductChemistry</title>
 <description>In Chapter 2, you have already learned that most drugs bind to the appropriate receptor molecules to exhibit their pharmacological actions, and also toxicity, which in fact is the adverse pharmacological action. A drug's pharmacological activity is inherently related to its chemical structure. Various functional groups present in the drug molecules are involved in the drug-receptor binding or interaction. For example, drugs containing hydroxyl or amino groups tend to be involved in hydrogen...&lt;p&gt;&lt;a href="http://www.arteleo.com/product/importance-of-functional-groups-in-determining-drug-actions-and-toxicity.html"&gt;&lt;img src="http://www.arteleo.com/product/images/1270_133_253.jpg" style="width: 240pt; height: 76pt;" title="The first sulpha drug nbsp SQ2NHR SQ3H nbsp Prontosil"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">The first sulpha drug nbsp SQ2NHR SQ3H nbsp Prontosil</media:description>
 <pubDate>Thu, 22 Sep 2011 09:54:06 GMT</pubDate>
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 <title>SCHEME Jul ChiralChemicals</title>
 <description>Another application of camphor-based chiral auxiliaries is the use in stereoselective Diels-Alder cycloadditions Chapter 26 , especially for the construction of quaternary carbon centers. One example, shown in Scheme 5.12, uses a camphor-derived lactam 30 as the auxiliary.54 Optically active menthols are also commonly used as chiral auxiliaries in industrial production of fine chemicals. The most recent example of using this inexpensive and readily available monoter-pene as chiral auxiliary for...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 09:39:43 GMT</pubDate>
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 <title>A Uxw Carbohydrates</title>
 <description>15218-38-9 Amino sugar antibiotic. Produced by several Streptomyces spp. Primarily active against gram-positive bacteria. Sol. H2O fairly sol. MeOH, EtOH poorly sol. butanol, hexane. Mp 126-130 dec. a D4 100 3 min. - gt 73.5 20 hr. . LD50 mus, ipr 1600 mg kg LD50 mus, ivn 1250 mg kg. LZ5655000 1-Deoxy See H-175 Mp 122-124 . a D0 -72.1 c, 0.3 in H2O . Inouye, S. et al., J. Antibiot., 1966, 19, 288 struct, nmr Saeki, H. et al., Chem. Pharm. Bull., 1968, 16, 962 synth Inouye, S. et al.,...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=t7dgE2N1s5M:8hl8AmKTOr0:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=t7dgE2N1s5M:8hl8AmKTOr0:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 09:10:01 GMT</pubDate>
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 <title>SUGGESTED ADDITIONAL READING Fjz Chromatography</title>
 <description>Arthur, C. Potter, D. Buchholz, K. Motlagh, S. Pawliszyn, J. Solid phase microextraction for the direct analysis of water Theory and practice. LC GC 1992, 10 9 , 656-661. Barker, S.A. Matrix solid-phase dispersion. J. Chromatogr., A 2000, 885, 115-127. Blevins, D.D. Hall, D.O. Recent advances in disk format solidphase extraction. LC GC 1998, 13 5 , S16-S21. Eskilsson, C.S. Bjorklund, E. Analytical-scale microwave-assisted extraction. J. Chromatogr., A 2000, 902, 227 -250. Georga, K.A....&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=xvwtGVA_Grc:2WYz_uj1S1g:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=xvwtGVA_Grc:2WYz_uj1S1g:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 08:53:15 GMT</pubDate>
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 <title>Oxidation with Singlet Oxygen FoodChemistry</title>
 <description>As just discussed, the major pathway for oxidation of unsaturated fatty acids involves a self-catalytic free-radical mechanism autoxidation that accounts for the chain reaction of hydroperoxide ROOH formation and decomposition. However, the origin of the initial free radicals necessary to begin the process has been difficult to explain. It is unlikely that initiation occurs by direct attack of oxygen in its most stable form triplet state on double bonds of fatty acids RH . This is because the C...&lt;p&gt;&lt;a href="http://www.arteleo.com/food/oxidation-with-singlet-oxygen.html"&gt;&lt;img src="http://www.arteleo.com/food/images/1370_142_175.jpg" style="width: 253pt; height: 65pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 08:29:11 GMT</pubDate>
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 <title>Conventional Transition State Theory Computational Chemistry 5</title>
 <description>Transition state theory TST , also known as conventional TST, goes back to the papers of Eyring8 and Evans and Polanyi9 in 1935. For a general gas-phase reaction of the type where A and B may be either atoms or molecules, the theory assumes that there is an activated complex called the transition state that represents the bottleneck in the reaction process. The fundamental assumption of TST also called the no-recrossing assumption is only expressible in classical mechanics. It states that 1...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 08:22:30 GMT</pubDate>
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 <title>Info Rak ChemicalDynamics</title>
 <description>H2 C4H2S Translational Energy Distribution P Er . The curve represents the normalized product flux as a function of total center-of-mass translational energy for the H C4H2S dissociation channel. This P Er could have some contribution from misinterpretation of dimer dissociation signal see text . Fig. 3-4. C2H2S C2H2 Time-of-Flight Spectra. The m e 58 C,H2S spectrum at 30 is shown in the top half of the figure. The spectrum for the conjugate QH2 fragment is shown in the m e 26, 50 in the lower...&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=51a9RrUR6GA:7V_YkGuRIHs:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=51a9RrUR6GA:7V_YkGuRIHs:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 08:20:10 GMT</pubDate>
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 <title>References 1 HeterocyclicCompounds</title>
 <description>Information was gleaned from each original publication except where an additional reference to Chemical Abstracts is included. Each citation of a Russian journal or Angewandte Chemie refers to the original Russian or German version, not to any subsequent English translation. Abbreviations for journal titles are those recommended in the Chemical Abstracts Service Source Index 1994 and quarterly supplements. 1. M. J. Grabowski, A. Stepien, M. Cygler, and E. Wajsman, Acta Crystallogr., Sect. B,...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 08:15:37 GMT</pubDate>
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 <title>TABLE Uid ChemicalProperties</title>
 <description>Li K Ca Na Mg Al Mn Zn Cr Fe Cd Co Ni Sn Pb H2 Sb Cu Hg Ag Pt Au Cr3 , Cr6 Fe2 , Fe3 Cd2 Co2 Ni2 A large piece of zinc metal is placed in a copper II sulfate, CuSO4, solution. The blue solution becomes colorless as copper metal falls to the bottom of the container. The resulting solution contains zinc sulfate, ZnSO4. Write balanced formula unit, total ionic, and net ionic equations for the reaction. The metals zinc and copper are not ionized or dissociated in contact with H2O. Both CuSO4 and...&lt;p&gt;&lt;a href="http://www.arteleo.com/chemical-properties/table-uid.html"&gt;&lt;img src="http://www.arteleo.com/chemical-properties/images/1385_765_123.jpg" style="width: 146pt; height: 144pt;" title="H2SO4 can function oxidizing agent with other substances but not oxidizing agent its reaction with active metals"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">H2SO4 can function oxidizing agent with other substances but not oxidizing agent its reaction with active metals</media:description>
 <pubDate>Thu, 22 Sep 2011 08:10:23 GMT</pubDate>
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 <title>Reactions of monosaccharides as alcohols ProductChemistry</title>
 <description>Monosaccharides contain a number of alcoholic hydroxyl groups, and thus can react with acid anhydrides to yield corresponding esters. For example, when glucose is treated with acetic anhydride and pyridine, it forms a pentaacetate. The ester functions in glucopyranose pentaacetate undergo the typical ester reactions. pentaacetate Monosaccharides also form phosphate esters with phosphoric acid. Mono-saccharide phosphate esters are important molecules in biological system. For example, in the DNA...&lt;p&gt;&lt;a href="http://www.arteleo.com/product/reactions-of-monosaccharides-as-alcohols.html"&gt;&lt;img src="http://www.arteleo.com/product/images/1270_225_362.jpg" style="width: 42pt; height: 29pt;"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
&lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=8i4VBQoCAq4:BS0AnDngyOs:yIl2AUoC8zA"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=yIl2AUoC8zA" border="0"&gt;&lt;/img&gt;&lt;/a&gt; &lt;a href="http://feeds.feedburner.com/~ff/ChemistryJournal?a=8i4VBQoCAq4:BS0AnDngyOs:qj6IDK7rITs"&gt;&lt;img src="http://feeds.feedburner.com/~ff/ChemistryJournal?d=qj6IDK7rITs" border="0"&gt;&lt;/img&gt;&lt;/a&gt;
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 <pubDate>Thu, 22 Sep 2011 07:56:14 GMT</pubDate>
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 <title>Info Bxs DistillationProcesses</title>
 <description>Fig. 59. The effect of packing fraction on heat transfer coefficient and mass flux of ideal hollow fiber module. Fig. 59. The effect of packing fraction on heat transfer coefficient and mass flux of ideal hollow fiber module. It can be seen from Fig. 58 lhat packing fraction has a significant effect on the performance of a non-uniformly packed module. There are two possible reasons for the mass flux enhancement by increasing packing fraction. It is known lhat heat transfer at the shell side can...&lt;p&gt;&lt;a href="http://www.arteleo.com/distillation-processes/info-bxs.html"&gt;&lt;img src="http://www.arteleo.com/distillation-processes/images/1663_2483_150.jpg" style="width: 307pt; height: 345pt;" title="Fig The effect packing fraction heat transfer coefficient and mass flux ideal hollow fiber module"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <media:description type="html">Fig The effect packing fraction heat transfer coefficient and mass flux ideal hollow fiber module</media:description>
 <pubDate>Thu, 22 Sep 2011 07:51:04 GMT</pubDate>
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 <title>REFERENCES Vjz Chromatography</title>
 <description>1. Nagy, D.J. J. Appl. Polym. Sci. 1996, 62 5 , 845. 2. Toussaint, B. Duchateau, A.L.L. van der Wal, Sj. Albert, A. Hubert, Ph. Crommen, J. J. Chromatogr., A 2000, 890, 239-249. 3. Risley, D.S. Strege, M.A. Anal. Chem. 2000, 72, 17361739. 4. Chen, S. Yuan, H. Grinberg, N. Dovletoglou, A. Bicker, Evaporative Light Scattering Detection for Liquid Chromatography G. J. Liq. Chromatogr. Relat. Technol. 2003, 26 3 , 425442. 5. Charlesworth, J. Anal. Chem. 1978, 50 11 , 1402-1414. 6. Righezza, M....&lt;div class="feedflare"&gt;
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 <title>CH Tmw HomogeneousCatalysis</title>
 <description>Figure 4.5. Diastereomeric alkene complexes with DIPAMP-Rh One can try to figure out from the pictures how two diastereomeric intermediates are formed. It is more convenient to adopt a formal approach. We can explain the formation of enantiomers when a metal even a bare Ag ion would do co-ordinates to our alkene substrate, and equally so the formation of diastereomers in Figure 4.5. Ligand intermezzo. A large series of asymmetric ligands have been developed most of which having the asymmetric...&lt;p&gt;&lt;a href="http://www.arteleo.com/homogeneous-catalysis/ch-tmw.html"&gt;&lt;img src="http://www.arteleo.com/homogeneous-catalysis/images/1437_265_64.jpg" style="width: 114pt; height: 66pt;" title="Figure Clutches having good fit"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 07:37:11 GMT</pubDate>
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 <title>Arrheniusabiding Aging Analytical Chemistry 3</title>
 <description>Introduction During the early stages of development of a dosage form or a drug substance one rarely has more than a notion of which temperatures the material will be processed or stored at once all has been said, done, and submitted. Also, the decomposition of a component might be subject to more than one mechanism, often with one reaction pathway dominating at lower, and another at higher temperatures. For these reasons, stress tests are conducted at a number of different temperatures that,...&lt;div class="feedflare"&gt;
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 <title>Unitary Transformations of the Dirac Hamiltonian 1 QuantumChemistry</title>
 <description>The separation of the spin-dependent terms in the Dirac Hamiltonian enables us to make an approximation in which the spin-free terms are included in the orbital optimization and the spin-dependent terms may be treated later as a perturbation. In this process, the parameter space required to treat the large and small components has not changed. Even with the extraction of a p from the small component, we still have to calculate integrals involving p4L, which essentially regenerates the original...&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 07:12:08 GMT</pubDate>
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 <title>Electrochemical Intercalation Electrochemistry</title>
 <description>Electrochemical intercalation is a process of incorporation of foreign species ions, atoms, or compounds into the bulk into the crystal lattice of solid electrodes hosts during their polarization. Deintercalation is the reverse process, removal of these species. As a result of the intercalation process, a new solid intercalation compound is formed with properties different from those of the host material. The intercalating species intercalates arrive either from the electrolyte or are formed in...&lt;p&gt;&lt;a href="http://www.arteleo.com/electrochemistry/electrochemical-intercalation.html"&gt;&lt;img src="http://www.arteleo.com/electrochemistry/images/1380_1034_190.jpg" style="width: 108pt; height: 144pt;" title="Boris Kabanov 1904 1988"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;div class="feedflare"&gt;
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 <pubDate>Thu, 22 Sep 2011 06:46:27 GMT</pubDate>
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