Issue 6, 2007

Synthesis and complexation study of (1,4-linked)-homothiaisocalixnaphthalenes

Abstract

A series of new cavity-containing molecular receptors, “homothiaisocalixnaphthalenes” containing 2,3-dialkoxy-substituted naphthalene units, have been synthesized, and some of their complexation properties have been investigated. The syntheses of the octaethoxy- and n-octapropoxy-octahomotetrathiaisocalix[4]naphthalenes were accompanied by small amounts of the corresponding higher dodecahomohexathia homologues. All of the macrocycles which were synthesized were highly symmetrical and conformationally flexible. Although these new macrocycles were not effective hosts for C60- and C70-fullerenes or the tetramethylammonium cation, two of them were shown, in a limited study, to effectively bind with Ag+ and only modestly with Hg2+.

Graphical abstract: Synthesis and complexation study of (1,4-linked)-homothiaisocalixnaphthalenes

Supplementary files

Article information

Article type
Paper
Submitted
12 Feb 2007
Accepted
13 Mar 2007
First published
02 Apr 2007

New J. Chem., 2007,31, 921-926

Synthesis and complexation study of (1,4-linked)-homothiaisocalixnaphthalenes

H. Tran and P. E. Georghiou, New J. Chem., 2007, 31, 921 DOI: 10.1039/B702152F

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