Issue 33, 2022

Tributylphosphine-catalyzed aziridine-based cycloaddition polymerization toward thiacyclic polymers

Abstract

An organocatalytic cycloaddition polymerization approach for the facile synthesis of thiacyclic polymers is established in this work. Bis(N-sulfonyl aziridine)s and diisocyanates are employed as the monomers, and they undergo cycloaddition polymerizations smoothly in the presence of tributylphosphine. Different kinds of bis(N-sulfonyl aziridine)s, including 2,3-disubstituted and 2-substituted ones, are applicable for this polymerization. Two kinds of diisocyanates, 1,4-phenylene diisothiocyanate and 1,4-butane diisothiocyanate, are used, and the produced poly(thiazolidin-2-imine)s exhibited different photophysical properties. The synthesized poly(thiazolidin-2-imine)s with alkyl linkages are luminous in the solid state and in solution, but the aryl-linked ones are nonluminous. In addition, the luminescent polymer can serve as a selective and sensitive fluorescence sensor for Fe3+.

Graphical abstract: Tributylphosphine-catalyzed aziridine-based cycloaddition polymerization toward thiacyclic polymers

Supplementary files

Article information

Article type
Paper
Submitted
01 May 2022
Accepted
01 Aug 2022
First published
02 Aug 2022

Polym. Chem., 2022,13, 4809-4816

Tributylphosphine-catalyzed aziridine-based cycloaddition polymerization toward thiacyclic polymers

Z. Zhou, Y. Wang, L. Zhu, D. Dang and Z. Zhang, Polym. Chem., 2022, 13, 4809 DOI: 10.1039/D2PY00569G

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