Abstract
The reaction of HTIMP(3) (HTIMP(3) = tris[1-(diphenylphosphino)-3-methyl-1H-indol-2-yl]methane) with [RhCl(COD)](2) and Rh(acac)(CO)(2) produces RhHCl(TIMP(3)) (1H) and Rh(TIMP(3))(CO) (2), respectively, both exhibiting tetradentate kappaC,kappa(3)P-coordination of the TIMP(3) moiety. The reaction of RhHCl(TIMP(3)) with nucleophiles (L) in the presence of AgBF(4) or AgPF(6) produces different compounds depending on the nature of L. Indeed, cationic Lewis adducts of formula [RhH(L)(TIMP(3))](+) ((2H+)-(5H+)) are obtained when L is CO, CNCH(2)Ph, pyridine or CH(2)CHCN. On the other hand, when the incoming nucleophile is CH(3)COOH the hydride-free complex [Rh(CH(3)COO)(TIMP(3))](+) ((6+)) is obtained. Finally, the reaction of RhHCl(TIMP(3)) with PhCCPh and CH(2)CHCOOMe in the presence of AgPF(6) leads to the insertion products [Rh(PhCCHPh)(TIMP(3))](+) ((+)) and [Rh(CH(2)CH(2)COOMe)(TIMP(3))](+) ((8+)), respectively. The solid state structure has been determined by single crystal X-ray diffraction in selected cases (1H, (6+)).
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