Literature DB >> 12381187

A versatile approach to affinitychromic polythiophenes.

Stéphanie Bernier1, Sébastien Garreau, Maïté Béra-Abérem, Catherine Gravel, Mario Leclerc.   

Abstract

The preparation of both postfunctionalizable and chromic poly[3-(N-succinimido-p-phenylcarboxylate(tetraethoxy)oxy)-4-methylthiophene] is reported. The N-hydroxysuccinimide ester side group can easily react with different amine-bearing molecules in the solid state to yield a library of new polythiophene derivatives. The resulting polymers can be dissolved in various solvents, and interactions between the side chains (ligands) and different analytes (targets) can be detected from modifications of both the side-chain and the backbone conformations resulting in important color changes (i.e., affinitychromism). This colorimetric polymeric transducer could therefore lead to highly valuable, versatile, and inexpensive tools for highthroughput screening and drug discovery.

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Year:  2002        PMID: 12381187     DOI: 10.1021/ja027387l

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  1 in total

1.  Pentafluorobenzene end-group as a versatile handle for para fluoro "click" functionalization of polythiophenes.

Authors:  Pierre Boufflet; Abby Casey; Yiren Xia; Paul N Stavrinou; Martin Heeney
Journal:  Chem Sci       Date:  2016-12-15       Impact factor: 9.825

  1 in total

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