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Living Vinyl Addition Polymerization of Substituted Norbornenes by a t-Bu3P-Ligated Methylpalladium Complex

Author(s): Kim, D-G; Bell, A; Register, Richard A

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dc.contributor.authorKim, D-G-
dc.contributor.authorBell, A-
dc.contributor.authorRegister, Richard A-
dc.date.accessioned2020-04-03T20:11:45Z-
dc.date.available2020-04-03T20:11:45Z-
dc.date.issued2015en_US
dc.identifier.citationKim, D-G, Bell, A, Register, RA. (2015). Living Vinyl Addition Polymerization of Substituted Norbornenes by a t-Bu<inf>3</inf>P-Ligated Methylpalladium Complex. ACS Macro Letters, 4 (327 - 330. doi:10.1021/acsmacrolett.5b00079en_US
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1vr4b-
dc.description.abstractThe vinyl addition polymerization of substituted norbornene (NB) monomers, via (t-Bu3P)PdMeCl activated by [Li(OEt2)2.5]B(C6F5)4, is investigated. NB monomers bearing alkyl, aryl, fluoroaryl, and even hexafluoroisopropanol substituents yield polymers exhibiting monomodal and narrow molecular weight distributions, with molecular weight controlled by reaction time and monomer to initiator ratio, demonstrating the living nature of these polymerizations. These polymers are soluble in common organic solvents and possess excellent thermal stability. Block copolymers are also prepared via sequential monomer addition; these are the first examples of well-defined block copolymers of substituted NB monomers enchained by vinyl addition polymerization. (Figure Presented).en_US
dc.format.extent327 - 330en_US
dc.language.isoen_USen_US
dc.relation.ispartofACS Macro Lettersen_US
dc.rightsFinal published version. This is an open access article.en_US
dc.titleLiving Vinyl Addition Polymerization of Substituted Norbornenes by a t-Bu<inf>3</inf>P-Ligated Methylpalladium Complexen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1021/acsmacrolett.5b00079-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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