期刊
ACS CATALYSIS
卷 8, 期 9, 页码 8182-8191出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.8b02122
关键词
olefin metathesis; ruthenium; sulfur-chelated benzylidenes; photoinduced catalysis; CAAC ligand; latency; double-bond isomerization
资金
- Israel Science Foundation
Sulfur-chelated ruthenium olefin metathesis precatalysts that possess cyclic (alkyl)(amino)carbenes (CAAC) can benefit from the synergetic effect of both ligands. Changing the steric bulk of the CAAC ligand by using different substitution patterns was shown to affect the geometry of the complexes produced and determined whether the complexes could be catalytically dormant. The cis-dichloro latent catalysts could be activated both by heat or light, even in the visible region, for representative acyclic diene metathesis and ring-opening metathesis polymerization reactions, olefin cross-metathesis, and ring-closing metathesis without isomerization byproducts. Thus, these complexes were shown to combine the uniqueness of CAAC-containing Ru olefin metathesis catalysts with the advantage of the thermal and photolatency imposed by sulfur chelation of the benzylidene.
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