JianFeng Li

Find an error

Name: 李建峰; Li, JianFeng
Organization: Nankai Univerisity , China
Department:
Title: Lecturer (PhD)

TOPICS

Co-reporter:Yinghua Shi;Chunming Cui
Dalton Transactions 2017 vol. 46(Issue 33) pp:10957-10962
Publication Date(Web):2017/08/22
DOI:10.1039/C7DT01837A
The dimeric heteroleptic ytterbium amido complex [(2,6-(3,5-Me2C6H3)2C6H3NH)Yb(N(SiMe3)2)]2 (1) has been prepared and characterized. This divalent terphenylamido complex enabled highly regioselective hydrosilylation of various terminal alkenes with very low catalyst loadings. The reaction of 1 with phenylsilane at high temperature led to the dehydrogenative coupling of silane with a terphenylamide ligand and redistributions of amide ligands via a hypervalent silane intermediate, which has been spectroscopically characterized.
Silanamine, N-[2,6-bis(1-methylethyl)phenyl]-N-[chloro[1,3-dihydro-4,5-dimethyl-1,3-bis(1-methylethyl)-2H-imidazol-2-ylidene]silyl]-1,1,1-trimethyl-
PHENYL(6-PHENYLSILYLHEXYL)SILANE
Pyridine, 2-[1,2-bis(diphenylphosphinyl)ethyl]-
Silane, phenyl(3-phenylpropyl)-
Silane, [1-(4-methoxyphenyl)ethyl]phenyl-
Silane, (cyclopentylmethyl)phenyl-
1,3-Di-tert-butyl-1H-imidazol-3-ium-2-ide
HEX-1-ENYL(DIPHENYL)PHOSPHANE
Silane, phenyl(1-phenylethyl)-