Systematic comparison of racemic and enantiopure multicomponent crystals of phenylsuccinic acid—the role of chirality
Author:
Affiliation:
1. Department of Chemistry
2. Cape Peninsula University of Technology
3. Cape Town
4. South Africa
Abstract
Comparison of binary cocrystals of chiral and racemic carboxylic acids showed that the introduction of chiral building blocks may lead to the formation of subclasses of multicomponent crystals with unique Z′′/Zr values combined with complex protonation stages of the molecules.
Funder
National Research Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
Condensed Matter Physics,General Materials Science,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/CE/D0CE00072H
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