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Ruthenium‐Catalyzed Alternating Ring‐Opening Metathesis Copolymerization of Norborn‐2‐ene with Cyclic Olefins
Author(s) -
Paradiso Veronica,
Grisi Fabia
Publication year - 2019
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201900565
Subject(s) - cyclopentene , carbene , metathesis , chemistry , ruthenium , chemoselectivity , cyclooctene , catalysis , ring opening metathesis polymerisation , polymer chemistry , copolymer , romp , ligand (biochemistry) , grubbs' catalyst , ring (chemistry) , organic chemistry , polymerization , biochemistry , receptor , polymer
A Grubbs‐type olefin metathesis catalyst bearing a backbone‐substituted unsymmetrical N‐heterocyclic carbene (NHC) ligand has been prepared from readily available reagents using a four‐step synthetic protocol. This catalyst was found able to promote the alternating ring‐opening metathesis copolymerization of norborn‐2‐ene (NBE) with cis ‐cyclooctene (COE) or cyclopentene (CPE) with a high degree of chemoselectivity (98% and 95% of alternating diads, respectively) at low comonomers ratios.

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