Issue 52, 2003
From the journal:

CrystEngComm

Unexpected isostructurality by permutation of classical and “weak” hydrogen bonds

Peter G. Jones*a  and  Fabiola Vanceaa  

* Corresponding authors

a Institut für Anorganische und Analytische Chemie, Technical University of Braunschweig, Postfach 3329, Braunschweig, Germany
E-mail: p.jones@tu-bs.de
Fax: +49-531-391-5387
Tel: +49-531-391-5382

Abstract

The compounds 2-chloromethylpyridinium chloride and 3-bromomethylpyridinium bromide are essentially isostructural despite their different substitution loci; the basic structural motif in both cases is a hydrogen-bonded dimer, but the positions of the classical and weak hydrogen bonds are interchanged.

Graphical abstract: Unexpected isostructurality by permutation of classical and “weak” hydrogen bonds

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DOI
https://doi.org/10.1039/B309038H
Article type
Paper
Submitted
30 Jul 2003
Accepted
07 Aug 2003
First published
18 Aug 2003

CrystEngComm, 2003,5, 303-304

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Unexpected isostructurality by permutation of classical and “weak” hydrogen bonds

P. G. Jones and F. Vancea, CrystEngComm, 2003, 5, 303 DOI: 10.1039/B309038H

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