Specific features of supramolecular organisation and hydrogen bonding in proline cocrystals: a case study of fenamates and diclofenac-Reference-Cited by-同舟云学术

Specific features of supramolecular organisation and hydrogen bonding in proline cocrystals: a case study of fenamates and diclofenac

Published:2018 Issue:43 Volume:20 Page:6970-6981
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Surov Artem O.¹²³^ORCID,Voronin Alexander P.¹²³^ORCID,Vener Mikhail V.⁴⁵³^ORCID,Churakov Andrei V.⁶⁷³^ORCID,Perlovich German L.¹²³^ORCID

Affiliation:

1. G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences

2. 153045 Ivanovo

3. Russia

4. Mendeleev University of Chemical Technology

5. 125047 Moscow

6. N.S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

7. Moscow

Abstract

New zwitterionic cocrystals of fenamate drugs and diclofenac with the naturally occurring amino acid l-proline have been obtained and thoroughly characterised by a variety of experimental and theoretical techniques.

Funder

Russian Foundation for Basic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CE/C8CE01458B

Reference84 articles.

1. Pharmaceutical cocrystals: along the path to improved medicines

2. Pharmaceutical cocrystals: walking the talk

3. Co-crystallization and small molecule crystal form diversity: from pharmaceutical to materials applications

4. Pharmaceutical cocrystals, salts and multicomponent systems; intermolecular interactions and property based design

5. L-Proline 2,5-Dihydroxybenzoic Acid (1/1): A Zwitterion Co-crystal.

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