Author： Byabartta Prithwiraj
Publisher： Springer Publishing Company
ISSN： 0340-4285
Source： Transition Metal Chemistry, Vol.30, Iss.6, 2005-09, pp. : 738-747
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Abstract
Ag+-assisted dechlorination of blue cis-trans-cis Ru(R-aai-R′)2Cl2 followed by the reaction with chloranilic acid (H2CA) in the presence of Et3N, gives a neutral mononuclear violet complex [Ru(R-aai-R′)2(CA)]. [R-aai-R′=p-R-C6H4—N=N—C3H2—NN, abbreviated as an N,N′ chelator where N(imidazole) and N(azo) represent N and N′, respectively; R = H (a), OMe (b), NO2 (c) and R′= Me (4), Et(5), Bz(6)]. All the complexes exhibit strong intense MLCT transitions in the visible region and weak broad bands at higher wavelength (>700 nm). Visible transitions (580–595 nm) show a negative solvatochromic effect. The cyclic voltammograms show two quasireversible to irreversible couples positive to SCE and are due to CA−/CA2− (1.2–1.35 V) and Ru(III)/Ru(II) (1.6–1.8 V) redox processes. Three couples, negative to SCE, are assigned to CA2−/CA3− (−0.2 to −0.3 V), and azo reductions (−0.5 to −0.7, −0.8 to −0.9 V) of the chelated R-aai-R′.
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