Controlled chain-growth polymerization via propargyl/allenyl palladium intermediates

In contrast to allyl palladium complexes, propargylic/allenylic palladium species display complex reactivities that limit their implementation in polymer chemistry, especially for chain-growth polymerizations. Here we report an example of controlled chain-growth polymerization via propargyl/allenyl palladium intermediates. Vinylidenecyclopropane 1,1-dicarboxylate (VDCP), a unique allenylic electrophile, selectively reacts via the σ-allenyl palladium complex rather than the more common π-propargyl pathway, thereby unlocking a chain-growth process. Based on this concept, precise synthesis of alkyne-backbone polymers is realized, featuring fast rate, high molecular weight, narrow dispersity, high chemoselectivity, and excellent end-group fidelity. We demonstrate preparation of unsaturated macromolecules with advanced sequences and architectures using this method, including block, gradient, and graft copolymers.

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Publication Details

Journal
Nature Communications
Published
2025-03-13
DOI
https://doi.org/10.1038/s41467-025-57723-8
Citations
2
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

Controlled chain-growth polymerization via propargyl/allenyl palladium intermediates

Zheng-Lin Wang, Rong Zhu
2 citations
Nature Communications
Synthetic Organic Chemistry Methods
1.87
article

Controlled chain-growth polymerization via propargyl/allenyl palladium intermediates

Zheng-Lin Wang, Rong Zhu
article en
2 citations

Abstract

In contrast to allyl palladium complexes, propargylic/allenylic palladium species display complex reactivities that limit their implementation in polymer chemistry, especially for chain-growth polymerizations. Here we report an example of controlled chain-growth polymerization via propargyl/allenyl palladium intermediates. Vinylidenecyclopropane 1,1-dicarboxylate (VDCP), a unique allenylic electrophile, selectively reacts via the σ-allenyl palladium complex rather than the more common π-propargyl pathway, thereby unlocking a chain-growth process. Based on this concept, precise synthesis of alkyne-backbone polymers is realized, featuring fast rate, high molecular weight, narrow dispersity, high chemoselectivity, and excellent end-group fidelity. We demonstrate preparation of unsaturated macromolecules with advanced sequences and architectures using this method, including block, gradient, and graft copolymers.

Nature CommunicationsVol. 16(1)
Peking University (CN), Beijing National Laboratory for Molecular Sciences (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality
Openalex Percentile: Top 17%
Synthetic Organic Chemistry Methods
1.87
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