Issue 18, 2006

Hydrogen-bonded dimers of a thiacalixarene substituted by carbamoylmethylphosphineoxide groups at the wide rim

Abstract

A thiacalix[4]arene derivative bearing four carbamoylmethylphosphineoxide groups at the wide rim forms hydrogen-bonded, dimeric capsules with S8 symmetry in the crystalline state and in apolar solvents, where the inclusion of cationic guests could be proved by 1H NMR and ESI mass spectra.

Graphical abstract: Hydrogen-bonded dimers of a thiacalixarene substituted by carbamoylmethylphosphineoxide groups at the wide rim

Supplementary files

Article information

Article type
Communication
Submitted
23 Jan 2006
Accepted
08 Mar 2006
First published
23 Mar 2006

Chem. Commun., 2006, 1932-1934

Hydrogen-bonded dimers of a thiacalixarene substituted by carbamoylmethylphosphineoxide groups at the wide rim

O. Kasyan, V. Kalchenko, M. Bolte and V. Böhmer, Chem. Commun., 2006, 1932 DOI: 10.1039/B601016D

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