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Cited by 292

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Diels−Alder Reactions with Novel Polymeric Dienes and Dienophiles: Synthesis of Reversibly Cross-Linked Elastomers

Gheneim, Rana, Perez-Berumen, Catalina, Gandini, Alessandro·2002·Macromolecules

Abstract

Novel highly flexible copolymers bearing dienic or dienophilic moieties were prepared by either free radical copolymerization of hexyl acrylate and 2-furfuryl methacrylate or the chemical modification of siloxane copolymers with pendant primary propylamino functions. In addition, maleimides were synthesized from oligoether bis(amine)s and from the amino pendant groups of the polysiloxane. Diels−Alder reactions between these copolymers and difunctional complementary coupling agents produced cross-linked elastomers in high yields. The thermal reversible character of these networks was confirmed by applying retro-Diels−Alder reactions in the presence of appropriate trapping reagents which restored the initial linear polymers quantitatively.

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Metadata

Authors
Gheneim, R., Perez-Berumen, C., & Gandini, A.
Venue
Macromolecules
Published
2002-08-08
Volume
35
Issue
19
Pages
7246-7253
ISSN
  • 0024-9297 (ISSN-L)
  • 1520-5835
OpenAlex
W1983596263
Cited by
292
References
9
FWCI
4.16
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Diels−Alder Reactions with Novel Polymeric Dienes and Dienophiles: Synthesis of Reversibly Cross-Linked Elastomers. https://app.cochat.ai/papers/10.1021/ma020343c
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Gheneim, R., Perez-Berumen, C., & Gandini, A. (2002). Diels−Alder Reactions with Novel Polymeric Dienes and Dienophiles: Synthesis of Reversibly Cross-Linked Elastomers. Macromolecules. https://doi.org/10.1021/ma020343c

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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.