Thermally or Photochemically Induced Reductive Cleavage of Metal−Metal Bonds of Metal Carbonyl Dimers by a Titanocene(III)tert-Butoxide:  Novel Reversible Access to Heterobimetallic Complexes

2003 ◽  
Vol 22 (7) ◽  
pp. 1376-1382 ◽  
Author(s):  
Kouki Matsubara ◽  
Shota Niibayashi ◽  
Hideo Nagashima
1979 ◽  
Vol 34 (9) ◽  
pp. 1195-1198 ◽  
Author(s):  
Thomas Madach ◽  
Heinrich Vahrenkamp

The oxidations and reductions of 27 singly arsenic bridged dinuclear metal carbonyl complexes were investigated. There are indications that the complexes as a whole are involved in the redox process. However, the expected one and two electron oxidations with concomitant formation of metal-metal bonds were not observed. Electrochemical electron transfers were irreversible. Chemical oxidation and reduction of a selected example resulted in a series of products originating from the primary fission of one metal-arsenic bond.


1983 ◽  
Vol 36 (3) ◽  
pp. 613 ◽  
Author(s):  
AS Huffadine ◽  
BM Peake ◽  
BH Robinson ◽  
J Simpson

A number of polynuclear metal carbonyl complexes can be used as substrates for electron attachment reactions induced by the photoionization of N,N,N',N'-tetramethyl-p-phenylenediamine. Theproducts of such reactions are derived from metal carbonyl radicals produced by cleavage of the metal-metal bonds.


1994 ◽  
Author(s):  
Steven M. Barnett ◽  
Stephane H. Brienne ◽  
Ian S. Butler ◽  
Frederick W. Einstein ◽  
Mike C. Jennings ◽  
...  

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