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Synthesis of New Photoswitchable Tectons Based on Thiacalix[4]arene Azo Derivatives in the 1,3-Alternate Conformation

Synthesis of New Photoswitchable Tectons Based on Thiacalix[4]arene Azo Derivatives in the... The paper describes the first synthesis of molecular tectons, a series of ligands based on thiacalix[4]arenes in the 1,3-alternate stereoisomeric form containing photoswitchable azo groups in the side chain and carboxyl groups as potential binding sites for the synthesis of photoswitchable complexes and coordination polymers. In the case of p-tert-butylcalixarenes, the convergent approach is preferred. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Doklady Chemistry Springer Journals

Synthesis of New Photoswitchable Tectons Based on Thiacalix[4]arene Azo Derivatives in the 1,3-Alternate Conformation

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References (10)

Publisher
Springer Journals
Copyright
Copyright © 2018 by Pleiades Publishing, Ltd.
Subject
Chemistry; Chemistry/Food Science, general; Industrial Chemistry/Chemical Engineering
ISSN
0012-5008
eISSN
1608-3113
DOI
10.1134/S0012500818030023
Publisher site
See Article on Publisher Site

Abstract

The paper describes the first synthesis of molecular tectons, a series of ligands based on thiacalix[4]arenes in the 1,3-alternate stereoisomeric form containing photoswitchable azo groups in the side chain and carboxyl groups as potential binding sites for the synthesis of photoswitchable complexes and coordination polymers. In the case of p-tert-butylcalixarenes, the convergent approach is preferred.

Journal

Doklady ChemistrySpringer Journals

Published: Apr 23, 2018

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