Electron Transfer. 125. Intermediate Oxidation States in the Reduction of Chromium(VI) with Hypophosphite

1995 ◽  
Vol 34 (16) ◽  
pp. 4057-4061 ◽  
Author(s):  
Swapan K. Chandra ◽  
E. Gelerinter ◽  
E. S. Gould
1974 ◽  
Vol 96 (13) ◽  
pp. 4136-4142 ◽  
Author(s):  
Robert A. Scott ◽  
G. P. Haight ◽  
J. N. Cooper

2018 ◽  
Vol 69 (1) ◽  
pp. 231-252 ◽  
Author(s):  
Leah G. Dodson ◽  
Michael C. Thompson ◽  
J. Mathias Weber

1982 ◽  
Vol 37 (3) ◽  
pp. 324-331 ◽  
Author(s):  
Heindirk torn Dieck ◽  
Ewald Kühl

Abstract Carbonyl complexes of chromium, molybdenum and tungsten of the type DAD M(CO)4 with DAD - diazadiene (R-N=CR′-CR′=NR) are shown by cyclic voltammetry to undergo electron transfer reactions to [DAD M(CO)4]+ and [DAD M(CO)4]-. The rate of subsequent chemical reactions with nucleophiles or by loss of ligands depend on the sol-vent, the metal and the ligands' electronic and steric properties. Chromium(+I) is more readily stabilized than Mo(+I) or W(-I) while the opposite is true for the stability of the anions formed. The dimerisation of a low-coordinate species DAD Mo(CO)3 from the reduction of DAD Mo(CO)3(CH3CN) is detected electrochemically. The stabilization of oxidation states +1 and -I is briefly discussed in view of the DAD ligand properties.


ChemInform ◽  
1987 ◽  
Vol 18 (50) ◽  
Author(s):  
T. P. SMITH ◽  
D. J. IVERSON ◽  
M. W. DROEGE ◽  
K. S. KWAN ◽  
H. TAUBE

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