4.7 Article

The influence of polymer architecture in polymer mechanochemistry

Journal

CHEMICAL COMMUNICATIONS
Volume 57, Issue 53, Pages 6465-6474

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc02501e

Keywords

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Funding

  1. NRF, Korea through Creative Research Initiative Grant
  2. NRF, Korea through Nano-Material Technology Development Program
  3. NRF, Korea [NRF-2021R1A2C1006301]

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This Feature Article summarizes recent developments in utilizing polymer architecture to modulate mechanochemical reactions within polymers. Various well-defined architectures have been explored, including cyclic, intramolecularly cross-linked, dendritic, star, bottlebrush, and dendronized polymers. The focus is on describing the enhancement or suppression of mechanochemical reactivity, with respect to analogous linear polymers, as well as differences in solution- and solid-state behavior.
Polymer architecture is an important factor in polymer mechanochemistry. In this Feature Article, we summarize recent developments in utilizing polymer architecture to modulate mechanochemical reactions within polymers, or more specifically, the location and rates of bond scission events that lead to polymer fragmentation or mechanophore activation. Various well-defined architectures have been explored, including those of cyclic, intramolecularly cross-linked, dendritic, star, bottlebrush, and dendronized polymers. We primarily focus on describing the enhancement or suppression of mechanochemical reactivity, with respect to analogous linear polymers, as well as differences in solution- and solid-state behavior.

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