6533b7d0fe1ef96bd125a337

RESEARCH PRODUCT

Highly trans-stereospecific Isoprene Polymerization by Neodymium Borohydrido Catalysts

And Angela PereiraDenise Barbier-baudryMarc VisseauxFanny Bonnet

subject

Polymers and Plasticschemistry.chemical_element010402 general chemistry01 natural sciencesNeodymiumCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundStereospecificityPolymer chemistryMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryBimetallic stripIsoprene010405 organic chemistryChemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/PolymersPolymerizationHomogeneousStoichiometry

description

Highly stereospecific polymerization of isoprene was achieved using borohydridoneodymium complexes. In combination with stoichiometric amounts of dialkylmagnesium, Nd(BH4)3(THF)3 (1) and Cp*‘Nd(BH4)2(THF)2 (2) (Cp*‘ = C5Me4nPr) afford very efficient catalysts. The activity reaches 37300 (g of polyisoprene/mol of Nd)/h. Half-lanthanidocene 2 gives rise to polyisoprene, 98.5% trans-regular, the highest content yet described for a homogeneous organometallic catalyst. NMR experiments argue for the formation of bimetallic Nd(μ-BH4)Mg active species.

10.1021/ma047615rhttps://hal.science/hal-00106202