Issue 3, 2006

Selective enclathration of picoline isomers by a resorcinarene host

Abstract

The resorcinarene host 14,16,54,56-tetrahydroxy-2,4,6,8-tetrapentyl-34,36,74,76-tetra(p-toluene-sulfonyl-oxy)-1,3,5,7(1,3)-tetrabenzenacyclooctaphane forms inclusion compounds with 2-, 3- and 4-picoline. The structures of these inclusion complexes have been elucidated and compared, with some being found to additionally include water molecules as guests. Competition experiments were carried out to determine whether this host would selectively enclathrate any of the picolines and thus investigate the capability of this host for the separation of picoline isomers. A very interesting result was obtained for the 3-picoline versus 4-picoline competition experiment, which displays a concentration dependent selectivity, but instead of selective inclusion of the guest of higher concentration, it was in fact the guest of lower concentration in the solution which was preferentially enclathrated. This unusual result was explained in terms of solubilities of the clathrates in the two guests.

Graphical abstract: Selective enclathration of picoline isomers by a resorcinarene host

Supplementary files

Article information

Article type
Paper
Submitted
02 Feb 2006
Accepted
09 Mar 2006
First published
17 Mar 2006

CrystEngComm, 2006,8, 275-280

Selective enclathration of picoline isomers by a resorcinarene host

M. R. Caira, T. le Roex and L. R. Nassimbeni, CrystEngComm, 2006, 8, 275 DOI: 10.1039/B601560C

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