Abstract
1,8-Naphthyridine (napy) and terpyridine-analogous (N,N,C) tridentate ligands coordinated ruthenium (II) complexes, [Ru L(napy-κ 2 N, N′) (dmso)](PF 6) 2 ( 1: L= L 1= N″-methyl-4′-methylthio-2,2′:6′,4″-terpyridinium, 2: L = L 2 = N″-methyl-4′-methylthio-2,2′:6′,3″-terpyridinium) were prepared and their chemical and electrochemical properties were characterized. The structure of complex 1 was determined by X-ray crystallographic study, showing that it has a distorted octahedral coordination style. The cyclic voltammogram of 1 in DMF exhibited two reversible ligand-localized redox couples. On the other hand, the CV of 2 shows two irreversible cathodic peaks, due to the Ru–C bond of 2 containing the carbenic character. The IR spectra of 1 in CO 2-saturated CH 3CN showed the formation of Ru-(η 1-CO 2) and Ru–CO complexes under the controlled potential electrolysis of the solution at −1.44 V (vs. Fc/Fc +). The electrochemical reduction of CO 2 catalyzed by 1 at −1.54 V (vs. Fc/Fc +) in DMF-0.1 M Me 4NBF 4 produced CO with a small amount of HCO 2H.
Published Version
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