A Study of the Liquid and Solvent Properties of Optically Active and Racemic α-Methylbenzylamine
Author:
Affiliation:
1. Departments of Chemistry and Physics, University of Tennessee, Knoxville, Tennessee 37996
Publisher
American Chemical Society (ACS)
Subject
Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp072174%2B
Reference20 articles.
1. Phase equilibriums and PVT data for the methane-methanol system to 300 MPa and 240.degree.C
2. Discriminating interactions between chiral molecules in the liquid phase: effect on volumetric properties
3. On the validity of Wallach's rule: on the density and stability of racemic crystals compared with their chiral counterparts
4. Chiral discrimination in liquids II. Excess molar enthalpies of {(1 − x)A+ + xA−}, where A denotes fenchone or α-methylbenzylamine
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1. A New centrosymmetric supramolecular Hybrid Antimony (III)-based material :X-ray characterization, vibrational studies, theoretical (DFT and TD-DFT) studies, thermal behavior, opto-electric properties and atomic Hirshfeld surface analysis.;Journal of Molecular Structure;2024-11
2. Paradoxes of Symmetry: Homochirality; Cryptochiral Reactions; Chiral Field, Memory, and Induction; Chiral and Racemic Environment;Current Organic Chemistry;2017-03-30
3. Solvent effect on the optical rotation of (S)-(−)-α-methylbenzylamine;Russian Journal of General Chemistry;2014-02
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