The Separation of Racemic Crystals into Enantiomers by Chiral Block Copolymers


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MASTAI, Yitzhak, Miloš SEDLÁK, Helmut CÖLFEN, Markus ANTONIETTI, 2002. The Separation of Racemic Crystals into Enantiomers by Chiral Block Copolymers. In: Chemistry - A European Journal. 8(11), pp. 2429-2437. ISSN 0947-6539. eISSN 1521-3765. Available under: doi: 10.1002/1521-3765(20020603)8:11<2429::AID-CHEM2429>3.0.CO;2-6

@article{Mastai2002-06-03Separ-40432, title={The Separation of Racemic Crystals into Enantiomers by Chiral Block Copolymers}, year={2002}, doi={10.1002/1521-3765(20020603)8:11<2429::AID-CHEM2429>3.0.CO;2-6}, number={11}, volume={8}, issn={0947-6539}, journal={Chemistry - A European Journal}, pages={2429--2437}, author={Mastai, Yitzhak and Sedlák, Miloš and Cölfen, Helmut and Antonietti, Markus} }

<rdf:RDF xmlns:dcterms="" xmlns:dc="" xmlns:rdf="" xmlns:bibo="" xmlns:dspace="" xmlns:foaf="" xmlns:void="" xmlns:xsd="" > <rdf:Description rdf:about=""> <dc:contributor>Antonietti, Markus</dc:contributor> <dc:contributor>Cölfen, Helmut</dc:contributor> <dcterms:available rdf:datatype="">2017-10-26T14:00:32Z</dcterms:available> <dc:language>eng</dc:language> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:date rdf:datatype="">2017-10-26T14:00:32Z</dc:date> <dcterms:isPartOf rdf:resource=""/> <dcterms:issued>2002-06-03</dcterms:issued> <dc:contributor>Mastai, Yitzhak</dc:contributor> <dc:contributor>Sedlák, Miloš</dc:contributor> <dc:creator>Cölfen, Helmut</dc:creator> <dc:creator>Sedlák, Miloš</dc:creator> <bibo:uri rdf:resource=""/> <dcterms:abstract xml:lang="eng">A series of chiral double hydrophilic block copolymers (DHBCs) was synthesized and employed as additives in the crystallization of calcium tartrate tetrahydrate (CaT). We found that appropriate polymers can slow down the formation of the thermodynamically most stable racemic crystals as well as the formation of one of the pure enantiomeric crystals so that chiral separation by crystallization occurs even when racemic crystals can be formed. In addition, the presence of DHBCs results in major modifications of crystal morphology, creating unusual morphologies of higher complexity. Our study demonstrates the potential application of chiral DHBCs in the control of chirality throughout crystallization, in particular for racemic crystal systems, and also shows that enantiomeric excess of one enantiomer can be maximized by the kinetic control of crystallization.</dcterms:abstract> <foaf:homepage rdf:resource="http://localhost:8080/jspui"/> <dc:creator>Antonietti, Markus</dc:creator> <dcterms:title>The Separation of Racemic Crystals into Enantiomers by Chiral Block Copolymers</dcterms:title> <dspace:isPartOfCollection rdf:resource=""/> <dc:creator>Mastai, Yitzhak</dc:creator> </rdf:Description> </rdf:RDF>

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