Issue 1, 2014

Hydrogen bond-assisted solid-state formation of a salt-bridged calix[5]arene pseudo-dimer

Abstract

Co-crystallization of a carboxylcalix[5]arene in the presence of n-butylamine afforded the corresponding host–guest carboxylate–butylammonium salt-bridged complex as a result of a proton transfer process assisted by a second non-ionized calixarene molecule. The crystals isolated consist of a supramolecular pseudo-dimer in which a host–guest inclusion complex is connected to a formally neutral receptor molecule – hosting a solvent molecule in the aromatic cavity – via a strong negative charge-assisted H-bond between the carboxyl/carboxylate substituents present at the narrow rim of the two interacting calixarene molecules.

Graphical abstract: Hydrogen bond-assisted solid-state formation of a salt-bridged calix[5]arene pseudo-dimer

Supplementary files

Article information

Article type
Paper
Submitted
21 Aug 2013
Accepted
20 Oct 2013
First published
22 Oct 2013

CrystEngComm, 2014,16, 89-93

Hydrogen bond-assisted solid-state formation of a salt-bridged calix[5]arene pseudo-dimer

G. Brancatelli, S. Pappalardo, G. Gattuso, A. Notti, I. Pisagatti, M. F. Parisi and S. Geremia, CrystEngComm, 2014, 16, 89 DOI: 10.1039/C3CE41667D

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