Roles of a tetrahydroborate ligand in a facile route to ruthenium(ii) ethyl hydride complexes, and a kinetic study of ethane reductive elimination

2004 ◽  
pp. 3788-3797 ◽  
Author(s):  
Simon B. Duckett ◽  
J. Claire Lowe (née Stott) ◽  
John P. Lowe ◽  
Roger J. Mawby
1999 ◽  
Vol 38 (11) ◽  
pp. 2624-2631 ◽  
Author(s):  
K. Peter C. Vollhardt ◽  
J. Kevin Cammack ◽  
Adam J. Matzger ◽  
Andreas Bauer ◽  
Kenneth B. Capps ◽  
...  

1998 ◽  
Vol 53 (5-6) ◽  
pp. 587-598 ◽  
Author(s):  
Hans-Friedrich Klein ◽  
Stefan Haller ◽  
Hongjian Sun ◽  
Xiaoyan Li ◽  
Thomas Jung ◽  
...  

Abstract Salicylaldehyde derivatives and related β-hydroxo aldehydes CHO-CR=CR′-OH react with CoMe(PMe3)4 via oxidative substitution to form low-spin d6 complexes mer-CoH(CO-CR=CR-O)(PMe3)3. Reductive elimination of acyl and hydride functions from cis positions at the metal is less favourable than in carbonyl cobalt intermediates through a pronounced stabilization by neutral phosphane σ-donor and dianionic acylenolato chelate ligands. Reactions of the hydride complexes with iodomethane or with protic acids HX afford octahedral molecular complexes mer-CoX(CO-CR=CR′-O)(PMe3)3 (X =I, OAc) and mer-CoX(CO-CR=CR′-O)(PMe3)2 (X = OAc, O-CR′=CR-CHO) without opening of the acylenolato chelate ring.


1995 ◽  
Vol 14 (12) ◽  
pp. 5677-5685 ◽  
Author(s):  
Anthony D. Selmeczy ◽  
William D. Jones ◽  
Robert Osman ◽  
Robin Perutz

2008 ◽  
Vol 105 (12) ◽  
pp. 601-608
Author(s):  
Seung Min Han ◽  
Dong Joon Min ◽  
Joo Hyun Park ◽  
Jung Ho Park ◽  
Jong Min Park
Keyword(s):  

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