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Cited by 185

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Synthesis of Functional Polyolefins Using Cationic Bisphosphine Monoxide–Palladium Complexes

Carrow, Brad P., Nozaki, Kyoko·2012·Journal of the American Chemical Society

Abstract

The copolymerization of ethylene with polar vinyl monomers, such as vinyl acetate, acrylonitrile, vinyl ethers, and allyl monomers, was accomplished using cationic palladium complexes ligated by a bisphosphine monoxide (BPMO). The copolymers formed by these catalysts have highly linear microstructures and a random distribution of polar functional groups throughout the polymer chain. Our data demonstrate that cationic palladium complexes can exhibit good activity for polymerizations of polar monomers, in contrast to cationic α-diimine palladium complexes (Brookhart-type) that are not applicable to industrially relevant polar monomers beyond acrylates. Additionally, the studies reported here point out that phosphine-sulfonate ligated palladium complexes are no longer the singular family of catalysts that can promote the reaction of ethylene with many polar vinyl monomers to form linear functional polyolefins.

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Metadata

Authors
Carrow, B. P., & Nozaki, K.
Venue
Journal of the American Chemical Society
Published
2012-05-16
Volume
134
Issue
21
Pages
8802-8805
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2326456169
Cited by
185
References
0
FWCI
5.10
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Synthesis of Functional Polyolefins Using Cationic Bisphosphine Monoxide–Palladium Complexes. https://app.cochat.ai/papers/10.1021/ja303507t
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Carrow, B. P., & Nozaki, K. (2012). Synthesis of Functional Polyolefins Using Cationic Bisphosphine Monoxide–Palladium Complexes. Journal of the American Chemical Society. https://doi.org/10.1021/ja303507t

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.