Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Michael B. Ghebreab"'
Publikováno v:
Journal of the American Chemical Society. 136:9240-9243
Catalytic hydrophosphination of terminal alkenes and dienes with primary phosphines (RPH2; R = Cy, Ph) under mild conditions has been demonstrated using a zirconium complex, [κ(5)-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH]Zr (1). Exclusively anti-Mar
Publikováno v:
Polyhedron. 29:42-45
The readily prepared zirconium complex, [κ5-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH2]Zr (1), is an effective precatalyst in the dehydrocoupling of o-bisphosphinobenzene and 1,2-bisphosphinoethane to the known intercalated products. The phosphanido complex (N
Autor:
Jillian J. Davidson, Tamila Shalumova, Russell P. Hughes, L. Taylor Elrod, Joseph M. Tanski, Rory Waterman, Michael B. Ghebreab, Andrew J. Roering, Samantha N. MacMillan, Stephanie M. Chan, Annalese F. Maddox, Kyle L. Donovan
Publikováno v:
Organometallics. 28:573-581
A homoleptic triamidoamine zirconium complex featuring a metalated trimethylsilyl substituent, [κ5-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH2]Zr (1), was synthesized by reaction of Zr(CH2Ph)4 with N(CH2CH2NHSiMe3)3 followed by sublimation. Complex 1 is a gener
Autor:
Arne Ficks, Christine A. Bange, Michael B. Ghebreab, Rory Waterman, Neil T. Mucha, Lee J. Higham
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 45(5)
Catalytic hydrophosphination of alkenes using a chiral, air-stable primary phosphine, (R)-[2'-methoxy(1,1'-binapthalen)-2-yl]phosphine, (R)-MeO-MOPH2, proceeds under mild conditions with a zirconium catalyst, [κ(5)-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NS
Publikováno v:
ChemInform. 46
Catalytic hydrophosphination of terminal alkenes and dienes with primary phosphines (RPH2; R = Cy, Ph) under mild conditions has been demonstrated using a zirconium complex, [κ5-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH]Zr (1). Exclusively anti-Marko
Publikováno v:
Dalton Transactions. 40:7683
Relating to the catalytic dehydrocoupling of secondary phosphine substrates, zirconium phosphide complexes supported by triamidoamine and pentamethylcyclopentadienyl ligands exhibit different stability that is attributed to β-hydride elimination.
Autor:
Andrew J. Roering, Annalese F. Maddox, L. Taylor Elrod, Stephanie M. Chan, Michael B. Ghebreab, Kyle L. Donovan, Jillian J. Davidson, Russell P. Hughes, Tamila Shalumova, Samantha N. MacMillan, Joseph M. Tanski, Rory Waterman
Publikováno v:
Organometallics; Jan2009, Vol. 28 Issue 2, p573-581, 9p
Publikováno v:
Dalton Transactions: An International Journal of Inorganic Chemistry; Jul2011, Vol. 40 Issue 30, p7683-7685, 3p