Alternating Copolymerization of Arynes and Aldehydes Enabled by an N -Arylamine Initiator

Abstract Here, we report the direct alternating copolymerization of arynes and aldehydes initiated by a simple N-arylamine. The N-arylamine framework is critical for suppressing competing aryne homopolymerization and promotes selective alternating polymerization through a Smiles-type rearrangement pathway. Regeneration of a neutral N-arylamine chain end during each propagation cycle enables complex polymer architectures, including block copolymers and cyclic polymers, through ring-expansion alternating copolymerization. The resulting polymers contain embedded ether linkages that impart an acid-triggered degradability.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-09-21
DOI
https://doi.org/10.1021/jacs.6c13641
Primary Topic
Cyclization and Aryne Chemistry
Type
article
Field-Weighted Citation Impact
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article

Alternating Copolymerization of Arynes and Aldehydes Enabled by an N -Arylamine Initiator

Mamoru Tobisu, Hayato Fujimoto, Shisato Yamamura, R Murakami
Journal of the American Chemical Society
Cyclization and Aryne Chemistry
article

Alternating Copolymerization of Arynes and Aldehydes Enabled by an N -Arylamine Initiator

Mamoru Tobisu, Hayato Fujimoto, Shisato Yamamura, R Murakami
article en

Abstract

Abstract Here, we report the direct alternating copolymerization of arynes and aldehydes initiated by a simple N-arylamine. The N-arylamine framework is critical for suppressing competing aryne homopolymerization and promotes selective alternating polymerization through a Smiles-type rearrangement pathway. Regeneration of a neutral N-arylamine chain end during each propagation cycle enables complex polymer architectures, including block copolymers and cyclic polymers, through ring-expansion alternating copolymerization. The resulting polymers contain embedded ether linkages that impart an acid-triggered degradability.

Journal of the American Chemical Society
Osaka City University (JP), The University of Osaka (JP)
Openalex Percentile: Top 21%
Cyclization and Aryne Chemistry
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