Impact of chirality on peculiar ibuprofen molecular dynamics: hydrogen bonding organization and syn vs. anti carboxylic group conformations
Author:
Affiliation:
1. Univ. Lille
2. CNRS
3. INRA
4. ENSCL
5. UMR 8207 – UMET – Unité Matériaux et Transformations
6. CQFM and IN,CQE
7. Instituto Superior Técnico
8. Universidade de Lisboa
9. 1049-001 Lisboa
10. Portugal
Abstract
Impact of chirality (R and S enantiomers) on syn vs. anti carboxylic group conformations, hydrogen bond dimers and peculiar ibuprofen molecular dynamics.
Funder
Fundação para a Ciência e a Tecnologia
Interreg
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2018/CP/C8CP04837A
Reference57 articles.
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2. G. Coquerel and R.Tamura , in Disordered Pharmaceutical Materials , ed. M. Descamps , Wiley-VCH Verlag , 2016 , pp. 135–160
3. The effect of hydrogen bonding propensity and enantiomeric composition on the dynamics of supercooled ketoprofen – dielectric, rheological and NMR studies
4. Crystallization from the Amorphous State of a Pharmaceutical Compound: Impact of Chirality and Chemical Purity
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