Multicomponent crystals of nitrofurazone – when more is less

Kudzaishe N. Sharara; Kudzanai Nyamayaro; Merrill M. Wicht; Gerhard A. Venter; Nikoletta B. Báthori

doi:10.1039/C8CE01911H

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Multicomponent crystals of nitrofurazone – when more is less†

Kudzaishe N. Sharara,

^a Kudzanai Nyamayaro,

^a Merrill M. Wicht,

^a Gerhard A. Venter

^b and Nikoletta B. Báthori

*^a

Author affiliations

* Corresponding authors

^a Department of Chemistry, Cape Peninsula University of Technology, P.O. Box 652, Cape Town, South Africa
E-mail: bathorin@cput.ac.za
Fax: +27 21 460 3854
Tel: +27 21 460 8354

^b Scientific Computing Research Unit and Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa

Abstract

Multicomponent crystal formation of nitrofurazone, a conformationally flexible drug that is capable of forming various supramolecular synthons, was challenging when coformers were selected based on popular crystal engineering principles.

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Article information

DOI: https://doi.org/10.1039/C8CE01911H
Article type: Communication
Submitted: 07 Nov 2018
Accepted: 03 Jan 2019
First published: 03 Jan 2019

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CrystEngComm, 2019,21, 1091-1096

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Multicomponent crystals of nitrofurazone – when more is less

K. N. Sharara, K. Nyamayaro, M. M. Wicht, G. A. Venter and N. B. Báthori, CrystEngComm, 2019, 21, 1091 DOI: 10.1039/C8CE01911H

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CrystEngComm

Multicomponent crystals of nitrofurazone – when more is less†

Abstract

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Multicomponent crystals of nitrofurazone – when more is less

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