4.8 Article

Topology-Reset Execution: Repeatable Postcyclization Recyclization of Cyclic Polymers

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 1, 页码 144-148

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201809621

关键词

cyclic polymers; macromolecular architectures; photochemistry; polymers; rheology

资金

  1. JSPS [18H04479]
  2. JSPS KAKENHI [16K14074, 16H04032]
  3. Grants-in-Aid for Scientific Research [18H04479, 16K14074, 16H04032] Funding Source: KAKEN

向作者/读者索取更多资源

Repeatable topological transformation of polymers for the modulation of material functions is a challenge. We have developed a method for repeatedly resetting a cyclic macromolecular architecture to a linear architecture by photostimulation, namely, topology-reset execution (T-rex) based on the photochemistry of hexaarylbiimidazoles (HABIs). We synthesized cyclic poly(dimethylsiloxane)s (PDMSs) of various ring sizes with HABIs linked in the chains. UV irradiation of the cyclic PDMSs produced telechelic linear PDMSs with triphenylimidazolyl radical (TPIR) end groups. After termination of UV irradiation, end-to-end recyclization occurred by the recoupling of TPIRs. The cyclic PDMSs also responded to ultrasound, which decreased their molecular weight (MW) by site-specific cleavage of in-chain HABI moieties, and we are able to reset the MWs by subsequent phototriggered T-rex. Furthermore, T-rex enabled solvent-free switching of the rheological properties of the materials while retaining the liquid character of PDMS.

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