Synthesis, Characterization, and H-Bonding Abilities of Ruthenium(II) Complexes Bearing Bidentate NR,NH-Carbene/Phosphine Ligands

Two new diphenylphosphine-substituted benzimidazoles featuring an ethylene ( 2 ) or a methylene linker ( 5 ) between the benzimidazole and the phosphine have been prepared. These precursors for bidentate carbene/phosphine ligands react with [RuCp*(μ 3 -Cl)] 4 under tautomerization with formation of complexes of type [RuCp*Cl(L)] ([ 6 ] and [ 7 ], L = NR,NH-carbene/phosphine ligand). The crystal structures of [ 6 ] and [ 7 ] have been determined by X-ray diffraction. These studies revealed that the length of the bridge between the benzimidazol-2-ylidene and the phosphine determines the geometric parameters of the carbene/phosphine chelate ring and the donor properties of the phosphine. A 1 H NMR titration of complex [ 6 ] with DMPU revealed the formation of a (carbene)N−H···O(DMPU) hydrogen bond in solution.