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Cited by 319

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

A Facile Procedure for Controlling Monomer Sequence Distribution in Radical Chain Polymerizations

Pfeifer, Sebastian, Lutz, Jean-François·2007·Journal of the American Chemical Society

Abstract

A novel sequential copolymerization strategy was investigated for preparing macromolecules with programmed sequences of functional comonomers. Four different N -substituted maleimides ( N -propyl maleimide, N -benzyl maleimide, N -methyl maleimide, and N -[3,5-bis(trifluoromethyl)phenyl] maleimide) were consecutively added during the atom transfer radical polymerization of styrene performed at 110 °C in the presence of a catalyst composed of copper(I) bromide and 4,4‘-dinonyl)-2,2‘-bipyridine. Owing to the exceptional cross-propagation of N -substituted maleimides with styrene, the four functional comonomers could be sequentially incorporated in the growing polymer chains.

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Metadata

Authors
Pfeifer, S., & Lutz, J.-F.
Venue
Journal of the American Chemical Society
Published
2007-07-17
Volume
129
Issue
31
Pages
9542-9543
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2084326111
Cited by
319
References
2
FWCI
4.11
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A Facile Procedure for Controlling Monomer Sequence Distribution in Radical Chain Polymerizations. https://app.cochat.ai/papers/10.1021/ja0717616
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Pfeifer, S., & Lutz, J.-F. (2007). A Facile Procedure for Controlling Monomer Sequence Distribution in Radical Chain Polymerizations. Journal of the American Chemical Society. https://doi.org/10.1021/ja0717616

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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.