Issue 1, 2010
From the journal:

CrystEngComm

A predicted dimer-based polymorph of 10,11-dihydrocarbamazepine (Form IV)†

Jean-Baptiste Arlin,a   Andrea Johnston,a   Gary J. Miller,a   Alan R. Kennedy,b   Sarah L. Pricec  and  Alastair J. Florence*a  

* Corresponding authors

a Solid-State Research Group, Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, UK
E-mail: alastair.florence@strath.ac.uk
Fax: +0141-552-2565
Tel: +0141-548-4877

b WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow, UK

c Department of Chemistry, University College London, 20 Gordon St, London, UK

Abstract

A novel polymorph of 10,11-dihydrocarbamazepine (form IV), which had been predicted to be thermodynamically feasible, was obtained from the vapour phase and displays an R22(8) hydrogen bonded dimer motif in contrast to the catemeric motifs in forms I–III.

Graphical abstract: A predicted dimer-based polymorph of 10,11-dihydrocarbamazepine (Form IV)

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Article information

DOI
https://doi.org/10.1039/B914365C
Article type
Communication
Submitted
16 Jul 2009
Accepted
23 Sep 2009
First published
05 Oct 2009

CrystEngComm, 2010,12, 64-66

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A predicted dimer-based polymorph of 10,11-dihydrocarbamazepine (Form IV)

J. Arlin, A. Johnston, G. J. Miller, A. R. Kennedy, S. L. Price and A. J. Florence, CrystEngComm, 2010, 12, 64 DOI: 10.1039/B914365C

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