2 article(s) from Vidavsky, Yuval
DCPD (1) and ruthenium benzylidene catalyst 2.
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ROMP of dicyclopentadiene by a ruthenium alkylidene initiator.
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Top: DSC plot of PDCPD 24 hours after polymerization. Blue line: 1st heating–cooling cycle. Black l...
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Change in Tg for a representative PDCPD sample as a function of time.
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Intensity of exothermic peak as a function of rest time at room temperature for different samples.
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Peak intensity as function of age. Samples were analyzed every two weeks. The abnormal low intensit...
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Resting temperature effect. Blue columns: resting at room temperature. Orange columns: resting at −...
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Top: Sample after 1 week with ethyl vinyl ether. Bottom: Sample after 1 week with diethyl ether.
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Beilstein J. Org. Chem. 2015, 11, 1469–1474, doi:10.3762/bjoc.11.159
Light activated metathesis of trans-2-pentene.
Light induced generation of metathesis active species 2.
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Well-defined tungsten photoactive catalysts.
The first ruthenium based complexes for PROMP.
Cyclic strained alkenes for PROMP.
Proposed mechanism for photoactivation of sandwich complexes.
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Ruthenium and osmium complexes with p-cymene and phosphane ligands for PROMP.
Commercially available photoactive ruthenium precatalyst.
Some of the rings produced by photo-RCM.
Photopromoted ene-yne RCM by cationic allenylidene ruthenium complex 14.
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Dihydrofurans synthesised by photopromoted ene-yne RCM.
Ruthenium complexes with p-cymene and NHC ligands.
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Ruthenium NHC complexes for PROMP containing p-cymene and trifluroacetate (17, 19) or phenylisonitr...
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Photoactivated cationic ROMP precatalysts.
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Different monomers for PROMP.
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Proposed mechanism for photoinitiated polymerisation by 22 and 23.
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Light-induced cationic catalysts for ROMP.
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Sulfur chelated ruthenium benzylidene pre-catalysts for olefin metathesis.
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Proposed mechanism for the photoactivation of sulfur-chelated ruthenium benzylidene.
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Photoacid generators for photoinduced metathesis.
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Synthesis of precatalysts 36 and 37.
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Trapping of proposed intermediate 41.
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Encapsulated 39, isolated from the monomer.
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Beilstein J. Org. Chem. 2010, 6, 1106–1119, doi:10.3762/bjoc.6.127
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