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BielawskiChristopher W

Bielawski, Christopher W.
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Redox-switchable olefin cross metathesis (CM) reactions and acyclic diene metathesis (ADMET) polymerizations

Author(s)
Ryu, YeonkyeongShao, HuilingAhumada, GuillermoLiu, PengBielawski, Christopher W.
Issued Date
2019-10
DOI
10.1039/c9qm00391f
URI
https://scholarworks.unist.ac.kr/handle/201301/29061
Fulltext
https://pubs.rsc.org/en/content/articlelanding/2019/QM/C9QM00391F#!divAbstract
Citation
MATERIALS CHEMISTRY FRONTIERS, v.3, no.10, pp.2083 - 2089
Abstract
We show that redox-switchable catalysis may be used to control acyclic diene metathesis (ADMET) polymerizations and related reactions. A Ru(ii) complex was found to display catalytic activities that were dependent on the oxidation state of a quinone-containing ligand. While the neutral form of the complex was found to catalyze ADMET polymerizations at rates that were commensurate with a commercially-available catalyst, significantly lower activities were observed when the complex was reduced. Using the rate differential, a series of ADMET polymerizations were modulated by alternately reducing and oxidizing the catalyst over time. A similar approach was also used to regulate the molecular weights of the polymers produced. Cross metathesis reactions and computational studies were performed in parallel to gain a deeper understanding of the underlying redox-switchable chemistry.
Publisher
ROYAL SOC CHEMISTRY
ISSN
2052-1537
Keyword
RING-OPENING POLYMERIZATIONCATALYSTSISOMERIZATIONKINETICS

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