Unsymmetric Dinuclear RhI2 and RhIRhIII Complexes Supported by Tetraphosphine Ligands and Their Reactivity of Oxidative Protonation and Reductive Dechlorination.

Abstract

Two linear tetradentate phosphine ligands, meso-Ph2PCH2P(Ph)CH2XCH2P(Ph)CH2PPh2 (X = CH2 (meso-dpmppp), NBn (meso-dpmppmNBn; Bn = benzyl)) were utilized to synthesize unsymmetrical dinuclear RhI complexes, [Rh2Cl2(meso-dpmppp)(L)] (L = XylNC (1a), CO (1b)) and [Rh2Cl2(meso-dpmppmNBn)(L)] (L = XylNC (1c), CO (1d)), where electron-deficient RhI → RhI centers with 30 valence electrons are supported by a tetraphosphine in an unusual cis-/trans-P,P coordination mode. The RhI dimers of 1a-d were treated with HCl under air to afford the RhI → RhIII dimers with 32 e-, [Rh2Cl4(meso-dpmppp)(L)] (L = XylNC (4a), CO (4b)) and [Rh2Cl4(meso-dpmppmNBn)(L)] (L = XylNC (4c), CO (4d)), via intermediate hydride complexes, [{RhCl2(μ-H)RhCl(L)}(meso-dpmppp)] (L = XylNC (2a), CO (2b)) and [{RhCl2(μ-H)RhCl(L)}(meso-dpmppmNBn)] (L = XylNC (2c), CO (2d)), and [{Rh(H)Cl2(μ-Cl)Rh(L)}(meso-dpmppp)] (L = XylNC (3a), CO (3b)) and [{Rh(H)Cl2(μ-Cl)Rh(L)}(meso-dpmppmNBn)] (L = XylNC (3c), CO (3d)). The hydride intermediates 2 and 3 were monitored under nitrogen by 1H{31P} and 31P{1H} NMR techniques to reveal two reaction pathways depending on the terminal auxiliary ligand L. Further, the reductive dechlorination converting RhIRhIII (4b,d) to RhI2 (1b,d) was accomplished with a CO terminal ligand by reacting with various amines that acted as one-electron reducing agents through an inner-sphere electron transfer mechanism. DFT calculations were performed to elucidate the electronic structures of 1a-d and 4a-d and to estimate the structures of the hydride intermediate complexes 2 and 3.