Ruthenium monoterpyridine complexes with 2,6-bis(benzoxazol-2-yl)pyridine as an ancillary ligand: Synthesis, structure and spectral studies
2008
Abstract Ruthenium monoterpyridine complexes, [ 1 ] + and [ 2 ] 2+ , with 2,6-bis(benzoxazol-2-yl)pyridine as an ancillary ligand, L, have been synthesized and characterized by UV–Vis, FT-IR and 1 H NMR spectroscopic techniques. The formulations of the complexes were confirmed by the single crystal structure of their perchlorate salts. In both complexes, the Ru II center is hexa-coordinated in a distorted geometry. In complex [ 1 ] + , the ancillary ligand L behaves as a bidentate ligand; in [ 2 ] 2+ , however, it binds the metal center as a tridentate ligand. The central pyridine nitrogen of terpyridine (N p,trpy ) is in a cis position with respect to the central pyridine nitrogen of the ancillary ligand (N p,benz ) in complex [ 1 ] + and in a trans -position in complex [ 2 ] 2+ . The cis orientation of N p,trpy and N p,benz in complex [ 1 ] + forces L to behave as bidentate. The quasi-reversible Ru II /Ru III couple appears at 0.90 and 1.44 V versus SCE in the case of complex [ 1 ] + and [ 2 ] 2+ , respectively. [ 1 ] + , in the presence of aqueous AgNO 3 , affords [ 2 ] 2+ through an intramolecular dissociative interchange pathway.
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