Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Christine A. Bange"'
Autor:
Christine A. Bange, Neil T. Mucha, Morgan E. Cousins, Abigail C. Gehsmann, Anna Singer, Taylor Truax, Lee J. Higham, Rory Waterman
Publikováno v:
Inorganics, Vol 4, Iss 3, p 26 (2016)
Zirconium-catalyzed alkene hydrophosphination and dehydrocoupling with an air-stable, fluorescent primary phosphine 8-[(4-phosphino)phenyl]-4,4-dimethyl-1,3,5,7-tetramethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene furnishes fluorescent phosphine pro
Externí odkaz:
https://doaj.org/article/6c0d6bd34a5846169417babd1c3d82f6
Publikováno v:
European Journal of Inorganic Chemistry. 2019:1640-1643
Autor:
Christine A. Bange, Rory Waterman
Publikováno v:
Polyhedron. 156:31-34
The zirconium compound, [κ5-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH2]Zr (1) , catalyzes the hydroarsination of alkenes with primary arsines, previously unknown substrates for this transformation. Irradiation in the ultraviolet, near-UV, or visible
Autor:
Elizabeth R. Young, Rory Waterman, Christine A. Bange, Matthew A. Conger, Matthew D. Liptak, Bryan T. Novas
Publikováno v:
ACS Catalysis. 8:6230-6238
Catalytic hydrophosphination using [κ5-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH2]Zr (1) under photolysis substantially enhances activity and avails greater substrate scope. Quantitative conversions of alkenes to secondary phosphines are reached in a
Publikováno v:
Organometallics. 36:3891-3895
[CpFe(CO)2]2 (1) (Cp = η5-C5H5) is an effective precatalyst for the hydrophosphination of alkenes with Ph2PH under visible light irradiation, which appears to be a unique way to promote metal-catalyzed hydrophosphination. Additionally, 1 is a photoc
Autor:
Christine A. Bange, Rory Waterman
Publikováno v:
ACS Catalysis. 6:6413-6416
Catalytic double hydrophosphination of internal alkynes and primary phosphines is possible using a zirconium complex, [κ5-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH]Zr (1). The reaction proceeds via stepwise hydrophosphination to give vinyl phosphine
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
Autor:
Rory Waterman, Christine A. Bange
Publikováno v:
ChemInform. 47
Despite significant advances, metal-catalyzed hydrophosphination has ample room for discovery, growth, and development. Many of the key successes in metal-catalyzed hydrophosphination over the last decade have indicated what is needed and what is yet
Autor:
Christine A. Bange, Rory Waterman
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 22(36)
Despite significant advances, metal-catalyzed hydrophosphination has ample room for discovery, growth, and development. Many of the key successes in metal-catalyzed hydrophosphination over the last decade have indicated what is needed and what is yet
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 45(14)
Simple tin derivatives, Cp*2SnCl2 (1) and Ph2SnCl2 (2), catalyze the hydrophosphination of alkene substrates with diphenylphosphine. Competitive dehydrocoupling to give Ph4P2 was observed, but this side reaction can be mitigated when the catalysis is