Abstract

Three new complexes [Pt(dpop)(Cl) 2], [(Cl) 2Pt(dpop)Pt(Cl) 2] and [(bpy) 2Ru(dpop)Pt(Cl) 2](PF 6) 2 (dpop = dipyrido(2,3-a:3′,2′-h)phenazine) were prepared and studied. The electronic absorption spectra of the complexes display Pt dπ → dpop π* and Ru dπ → dpop π* MLCT transitions at longer wavelengths than for previously reported similar complexes. Results of cyclic voltammograms show reversible dpop centered reductions while for the mixed metal [(bpy) 2Ru(dpop)Pt(Cl) 2] 2+ an irreversible Pt(II) oxidative wave precedes the Ru(II) oxidation/reduction couple. Spectroelectrochemical results show that all oxidative and reductive processes are completely reversible. The [(Cl) 2Pt(dpop)Pt(Cl) 2] complex cleaves in solution with pseudo-first order kinetics resulting in loss of the Pt dπ → dpop π* MLCT transition at 545 nm.

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