Preparation and reactivity of dinuclear complexes having the M2(μ-Pz)(μ-SBut)(μ-dppm) core (M=Rh, Ir; Pz=pyrazolate)
- Pinillos, M.T. 1
- Elduque, A. 1
- Oro, L.A. 1
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1
Instituto de Nanociencia y Materiales de Aragón
info
ISSN: 0020-1693
Año de publicación: 1990
Volumen: 178
Número: 2
Páginas: 179-183
Tipo: Artículo
beta Ver similares en nube de resultadosOtras publicaciones en: Inorganica Chimica Acta
Resumen
The reaction of [M2(μ-Pz)(μ-SBut)(COD)2] with carbon monoxide and bis(diphenylphosphino)methane yields the triply heterobridged complexes [M2(μ-Pz)(μ-SBt)(μ-dppm)(CO)2], M=Rh, Pz=pz (1); M=Ir, Pz=pz (2), dmpz (3). The complexes 1-3 are oxidized by molecular iodine to [M2(μ-Pz)(μ-SBut)(μ-dppm)I2(CO)2], M=Rh, Pz=pz (4); M=Ir, Pz=pz (5), dmpz (6). Complexes 4-6 undergo halide abstraction with silver nitrate to form [M2(μ-Pz)(μ-SBut)(μ-dppm)(NO3)2(CO)2], M=Rh, Pz=pz (7); M=Ir, Pz=pz (8), dmpz (9). Complexes 2 and 3 react with mercury(II) chloride in 1:1 mole ratio to give the iridium(III)-iridium(I) complexes [Ir2(μ-Pz)(μ-SBut)(μ-dppm)(μ-HgCl)Cl(CO)2], Pz=pz (10), dmpz (11) resulting from oxidative addition of HgCl2 to one metal centre. Interaction of the mixed oxidation state complexes 10 and 11 with mercury(II) chloride affords the diiridium(II) compounds [Ir2(μ-Pz)(μ-SBut)(μ-dppm)Cl2(CO)2], Pz=pz (12), dmpz (13). © 1990.