Organometallic compounds of type [M(3)(CO)(7)(dppm)(tolan)], where M is Os or Ru, dppm is bis(diphenylphosphino)methane and tolan is 1,2-diphenyl-acetylene, have two isomers differing in the orientation of alkyne ligand with respect to the triangular metallic frame. The perpendicular isomer is stable in the oxidized state while the parallel isomer exists in the reduced state. The redox-induced isomerization causes two unusual adsorption waves to be observed on mercury in acetone solution. The osmium cluster gives two adsorption post-waves, whereas the ruthenium cluster gives one adsorption pre-wave and one post-wave. These effects are explained in terms of the different location of the isomerization reaction in the two-electron redox exchange.

Unusual twin adsorption waves in voltammetry of trimetallic clusters of Os and Ru undergoing redox-induced reorientation of the alkyne ligand

OSELLA, Domenico;NERVI, Carlo
1996-01-01

Abstract

Organometallic compounds of type [M(3)(CO)(7)(dppm)(tolan)], where M is Os or Ru, dppm is bis(diphenylphosphino)methane and tolan is 1,2-diphenyl-acetylene, have two isomers differing in the orientation of alkyne ligand with respect to the triangular metallic frame. The perpendicular isomer is stable in the oxidized state while the parallel isomer exists in the reduced state. The redox-induced isomerization causes two unusual adsorption waves to be observed on mercury in acetone solution. The osmium cluster gives two adsorption post-waves, whereas the ruthenium cluster gives one adsorption pre-wave and one post-wave. These effects are explained in terms of the different location of the isomerization reaction in the two-electron redox exchange.
1996
412
147
152
osmium; ruthenium; carbonyls; acetylene-type ligands; redox-induced isomerization; voltammetry
L. Pospisil; J. Fiedler; D. Osella; C. Nervi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/44462
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