Activation of H-H and H-O bonds at phosphorus with diiron complexes bearing pyramidal phosphinidene ligands.

The complex [Fe(2)Cp(2)(μ-PMes*)(μ-CO)(CO)(2)] (Mes* = 2,4,6-C(6)H(2)(t)Bu(3)), which in the solid state displays a pyramidal phosphinidene bridge, reacted at room temperature with H(2) (ca. 4 atm) to give the known phosphine complex [Fe(2)Cp(2)(μ-CO)(2)(CO)(PH(2)Mes*)] as the major product, along with small amounts of other byproducts arising from the thermal degradation of the starting material, such as the phosphindole complex [Fe(2)Cp(2)(μ-CO)(2)(CO){PH(CH(2)CMe(2))C(6)H(2)(t)Bu(2)}], the dimer [Fe(2)Cp(2)(CO)(4)], and free phosphine PH(2)Mes*. During the course of the reaction, trace amounts of the mononuclear phosphide complex [FeCp(CO)(2)(PHMes*)] were also detected, a compound later found to be the major product in the carbonylation of the parent phosphinidene complex, with this reaction also yielding the dimer [Fe(2)Cp(2)(CO)(4)] and the known diphosphene MesP═PMes. The outcome of the carbonylation reactions of the title complex could be rationalized by assuming the formation of an unstable tetracarbonyl intermediate [Fe(2)Cp(2)(μ-PMes*)(CO)(4)] (undetected) that would undergo a fast homolytic cleavage of a Fe-P bond, this being followed by subsequent evolution of the radical species so generated through either dimerization or reaction with trace amounts of water present in the reaction media. A more rational synthetic procedure for the phosphide complex was accomplished through deprotonation of the phosphine compound FeCp(CO)(2)(PH(2)Mes*) with Na(OH), the latter in turn being prepared via oxidation of [Fe(2)Cp(2)(CO)(4)] with FeCp(2) in the presence of PH(2)Mes*. To account for the hydrogenation of the parent phosphinidene complex it was assumed that, in solution, small amounts of an isomer displaying a terminal phosphinidene ligand would coexist with the more stable bridged form, a proposal supported by density functional theory (DFT) calculations of both isomers, with the latter also revealing that the frontier orbitals of the terminal isomer (only 5.7 kJ mol(-1) above of the bridged isomer, in toluene solution) have the right shapes to interact with the H(2) molecule. In contrast to the above behavior, the cyclohexylphosphinidene complex [Fe(2)Cp(2)(μ-PCy)(μ-CO)(CO)(2)] failed to react with H(2) under conditions comparable to those of its PMes* analogue. Instead, it slowly reacted with HOR (R = H, Et) to give the corresponding phosphinous acid (or ethyl phosphinite) complexes [Fe(2)Cp(2)(μ-CO)(2)(CO){PH(OR)Mes*}], a behavior not observed for the PMes* complex. The presence of BEt(3) increased significantly the rate of the above reaction, thus pointing to a pathway initiated with deprotonation of an O-H bond of the reagent by the basic P center of the phosphinidene complex, this being followed by the nucleophilic attack of the OR(-) anion at the P site of the transient cationic phosphide thus formed. The solid-state structure of the cis isomer of the ethanol derivative was determined through a single crystal X-ray diffraction study (Fe-Fe = 2.5112(8) Å, Fe-P = 2.149(1) Å).