Crystallisation and physicochemical property characterisation of conformationally-locked co-crystals of fenamic acid derivatives-Reference-Cited by-同舟云学术

Crystallisation and physicochemical property characterisation of conformationally-locked co-crystals of fenamic acid derivatives

Published:2015 Issue:19 Volume:17 Page:3610-3618
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Wittering K. E.¹²³⁴²,Agnew L. R.¹²³⁴²,Klapwijk A. R.¹²³⁴²,Robertson K.¹²³⁴²,Cousen A. J. P.¹²³⁴²,Cruickshank D. L.¹²³,Wilson C. C.¹²³⁴²

Affiliation:

1. Department of Chemistry

2. University of Bath

3. Bath, UK

4. Engineering and Physical Sciences Research Council (EPSRC) Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation (CMAC)

Abstract

Co-crystals of fenamic acid and its highly polymorphic derivatives with 4,4′-bipyridine are prepared using various crystallisation techniques and have been shown to afford single polymorphic forms for each of the co-crystals.

Funder

Engineering and Physical Sciences Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CE/C5CE00297D

Reference37 articles.

1. Nonamorphism in Flufenamic Acid and a New Record for a Polymorphic Compound with Solved Structures

2. Conformational Polymorphism in a Non-steroidal Anti-inflammatory Drug, Mefenamic Acid

3. Mefenamic Acid Anti-Inflammatory Drug: Probing Its Polymorphs by Vibrational (IR and Raman) and Solid-State NMR Spectroscopies