Carbon-carbon bond formation versus hydrogen transfer in the reaction of alkynes with mono(cyclopentadienyl)zirconium(II) complexes: regioselective dimerization, cocyclotrimerization, and catalytic cyclotrimerization. The preparation and x-ray structures of Cp(dmpe)XZr[(R)C:C(R')C(R):C(R')] [R = CH3; R' = H, CH3; X = Cl, CH3; dmpe = 1,2-bis(dimethylphosphino)ethane] and of CpZr(dmpe)Cl[C.tplbond.C(t-Bu)][CH:CH(t-Bu)]

Autor: Ytsen Wielstra, Sandro Gambarotta, Auke Meetsma, Jan L. De Boer, Michael Y. Chiang
Rok vydání: 1989
Předmět:
Zdroj: Organometallics. 8:2696-2702
ISSN: 1520-6041
0276-7333
DOI: 10.1021/om00113a028
Popis: La reaction de CpZr(dmpe) 2 X, [X=Cl, Me; dmpe=bis-dimethylphosphino ethane et d'alcynes aliphatiques donne le complexe CpZr(dmpe) Cl [C≡C(t-Bu)] [CH=CH(t-Bu)] et un derive de cyclopentadienyl-1 dimethyl-2,4 zirconacyclopentadiene-2,4. Ces complexes interviennent dans les reactions de cyclotrimerisation et cocyclotrimerisation de propyne, acetylene, acetonitrile
Databáze: OpenAIRE