4.5 Review

Complex polymer architectures through free-radical polymerization of multivinyl monomers

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NATURE REVIEWS CHEMISTRY
卷 4, 期 4, 页码 194-212

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41570-020-0170-7

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资金

  1. Science Foundation Ireland (SFI) [13/IA/1962]
  2. National Science Foundation (NSF) Division of Materials Research (DMR) [1501324]
  3. National Natural Science Foundation of China (NSFC) [51873179]
  4. State Key Laboratory of Molecular Engineering of Polymers, Fudan University [19FGJ07]
  5. Irish Research Council (IRC) Employment-Based Postgraduate Programme [EBPPG/2018/159]
  6. University College Dublin
  7. Direct For Mathematical & Physical Scien
  8. Division Of Materials Research [1501324] Funding Source: National Science Foundation
  9. Science Foundation Ireland (SFI) [13/IA/1962] Funding Source: Science Foundation Ireland (SFI)

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The construction of complex polymer architectures with well-defined topology, composition and functionality has been extensively explored as the molecular basis for the development of modern polymer materials. The unique reaction kinetics of free-radical polymerization leads to the concurrent formation of crosslinks between polymer chains and rings within an individual chain and, thus, free-radical (co)polymerization of multivinyl monomers provides a facile method to manipulate chain topology and functionality. Regulating the relative contribution of these intermolecular and intramolecular chain-propagation reactions is the key to the construction of architecturally complex polymers. This can be achieved through the design of new monomers or by spatially or kinetically controlling crosslinking reactions. These mechanisms enable the synthesis of various polymer architectures, including linear, cyclized, branched and star polymer chains, as well as crosslinked networks. In this Review, we highlight some of the contemporary experimental strategies to prepare complex polymer architectures using radical polymerization of multivinyl monomers. We also examine the recent development of characterization techniques for sub-chain connections in such complex macromolecules. Finally, we discuss how these crosslinking reactions have been engineered to generate advanced polymer materials for use in a variety of biomedical applications.

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