Synthesis, Structure and Inclusion Properties of distal-bis{[(5′-methyl-2,2′-bipyridyl)-5-yl]methoxy}tetrathiacalix[4]arene with 1,3-alternate Conformation

Author:

Shimizu Tomoe1,Rahman Shofiur1,Xi Zeng2,Yamato Takehiko1

Affiliation:

1. Department of Applied Chemistry, Faculty of Science and Engineering, Saga University, Honjo-machi 1, Saga-shi, Saga 840-8502, Japan

2. Key Laboratory of Macrocyclic and Supramolecular Chemistry of Guizhou Province, Guizhou University, Guiyang, Guizhou, 550025, P.R. China

Abstract

distal-Tetrathiacalix[4]arene having [(5′-methyl-2,2′-bipyridyl)-5-yl]methoxy group with 1,3- alternate conformation was prepared, which shows strong Ag+ affinity and the high Ag+ selectivity. The conformational change of 2,2′-bipyridyl moiety from the original outward orientation of the ring nitrogen to the inside orientation toward the thiacalixarene cavity was observed in the process of Ag+ complexation.

Publisher

SAGE Publications

Subject

General Chemistry

Reference44 articles.

1. Calixarenes: A Versatile Class of Macrocyclic Compounds

2. ShinkaiS., Advances in supramolecular chemistry, vol. 3, pp. 97, ed. GokelG.W., Jai Press Inc Ltd., London, 1993.

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