Publication:
Infrared Rotatory Dispersion of Liquid‐Crystalline Solutions of Chiral Molecules

dc.contributor.authorErnst‐Heiner ‐H Korteen_US
dc.contributor.authorBernhard Schraderen_US
dc.contributor.authorSauvarop Bualeken_US
dc.contributor.authorHans Jürgen Krabbeen_US
dc.contributor.otherInstitute for Analytical Sciences, Dortmunden_US
dc.contributor.otherUniversitat Duisburg-Essenen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherRWEen_US
dc.date.accessioned2018-03-22T09:29:03Z
dc.date.available2018-03-22T09:29:03Z
dc.date.issued1977-01-01en_US
dc.description.abstractThe absolute configuration of molecules with a chiral center can be established by a new empirical procedure: nematic phases of liquid‐crystalline compounds become cholesteric on dissolution of a chiral “guest substance”. The sign of the measured Reflection Cotton Effect provides information whether the three ligands of greatest priority a > b > c (see priority scheme) are arranged clockwise or counterclockwise. (Figure Presented.) Copyright © 1977 by Verlag Chemie, GmbH, Germanyen_US
dc.identifier.citationAngewandte Chemie International Edition in English. Vol.16, No.11 (1977), 790-791en_US
dc.identifier.doi10.1002/anie.197707901en_US
dc.identifier.issn15213773en_US
dc.identifier.issn05700833en_US
dc.identifier.other2-s2.0-84980136349en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/10247
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84980136349&origin=inwarden_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleInfrared Rotatory Dispersion of Liquid‐Crystalline Solutions of Chiral Moleculesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84980136349&origin=inwarden_US

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