A pentanuclear osmium complex with two adjacent, unusually short metal–metal bonds: the X-ray crystal structure of [HOs5(CO)13(PHNC6H4N)]

1980 ◽  
pp. 712-714 ◽  
Author(s):  
Zain Dawoodi ◽  
Martin J. Mays ◽  
Paul R. Raithby
Keyword(s):  
Crystal Structure ◽  
X Ray ◽  
Metal Metal ◽  
Metal Metal Bonds ◽  
Metal Bonds

Resonance Raman and X-ray Crystallographic Studies of Intertriad Metal−Metal Bonds. 2. WRu and MoOs Porphyrin Dimers

1999 ◽  
Vol 38 (9) ◽  
pp. 2093-2097 ◽  
Author(s):  
James P. Collman ◽  
S. T. Harford ◽  
Stefan Franzen ◽  
Andrew P. Shreve ◽  
William H. Woodruff
Keyword(s):  
Resonance Raman ◽  
X Ray ◽  
Metal Metal ◽  
Metal Metal Bonds ◽  
Metal Bonds ◽  
Porphyrin Dimers

Öffnung von Dreikernclustern durch Diphosphinomethan-Liganden / Opening of Trinuclear Clusters by Diphosphinomethane Ligands

1989 ◽  
Vol 44 (2) ◽  
pp. 139-144 ◽  
Author(s):  
Roy P. Planalp ◽  
Heinrich Vahrenkamp
Keyword(s):  
Crystal Structure ◽  
Structure Determination ◽  
Addition Product ◽  
Crystal Structure Determination ◽  
Metal Metal ◽  
Trinuclear Clusters ◽  
Metal Metal Bonds ◽  
Metal Bonds

Abstract The phosphinidene bridged clusters FeCo2(CO)9(PMe) and FeCoWCp(CO)8(PM e) add the diphosphinomethane ligands dmpm and dppm with concomitant opening of two metal-metal bonds. The crystal structure determination of the addition product (Me2P-CH2-PMe2)FeCoWCp(CO)8(PMe) has shown that the Fe -W and Fe -Co bonds have been opened and the chelating diphosphine spans the Co -W bond. This is in contrast to the reaction with monodentate phosphines where the Co -W and Co -Fe bonds are broken. Upon heating the addition products eliminate two moles of CO with formation of the diphos­ phinom ethane substituted starting clusters, which in turn add CO under pressure to re-form the addition products.

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