Unsymmetric Ir2 and RhIr Dinuclear Complexes Supported by a Linear Tetraphosphine meso-dpmppp, Showing High Reactivity for O2, H2, and HCl.

Abstract

Unsymmetric dinuclear Ir(I) complexes, [Ir2Cl2(L)(meso-dpmppp)] (L = XylNC (1aIr2), tBuNC (1bIr2), CO (1cIr2)), were synthesized using meso-Ph2PCH2P(Ph)(CH2)3P(Ph)CH2PPh2 (meso-dpmppp), which supports cis-P,P (M1) and trans-P,P (M2) metal sites, and exhibited high reactivity for O2, H2, and HCl. The IrRh heterodinuclear complexes, [M1M2Cl2(L)(meso-dpmppp)] (1xM1M2) (M1M2 = IrRh, RhIr; L = XylNC, CO (x = a, c)), were also synthesized and used together with the Rh2 complexes (1a,cRh2) to elucidate the role of each metal site. For the reactions of O2, 1aIr2 and 1aRhIr showed higher reactivity than those of 1aIrRh and 1aRh2, giving η2-peroxide complexes [{M1Cl2}{M2(η2-O2)(XylNC)}(meso-dpmppp)] (2aIr2, 2aRhIr), from which O2 would not dissociate. All the CO complexes 1cM1M2 (M1, M2 = Ir or Rh) showed no reactivity for O2. In the reactions with H2, 1aIr2 reacted with H2 to give the dihydride complex, [{IrCl2}{Ir(H)2L}(meso-dpmppp)] (11aIr2) and the tetrahydride complex, [{Ir(H)Cl2}(μ-H){Ir(H)2L}(meso-dpmppp)] (12aIr2), while 1aRhIr gave the dihydride complex, and 1aIrRh and 1aRh2 gave no hydride complexes. Reactions of 1a,cM1M2 with HCl afforded the dihydride complexes, [{IrCl3}(μ-H){Ir(H)Cl(XylNC)}(meso-dpmppp)] (14aIr2), [{Ir(H)Cl2}(μ-H){M2Cl2(L)}(meso-dpmppp)] (M2 = Ir, L = CO (15cIr2); M2 = Rh, L = XylNC (15aIrRh), CO (15cIrRh)), and [{Rh(H)Cl2}(μ-Cl){Ir(H)Cl(XylNC)}(meso-dpmppp)] (18aRhIr), the structures varying depending on M1 and M2 as well as L.