Rhenium(I) tricarbonyl complexes with bispyridine ligands attached to sulfur-rich core: Syntheses, structures and properties

Abstract

Abstract Rhenium(I) tricarbonyl complexes with bispyridine ligands bearing sulfur-rich pendant, Re(CO)3(Medpydt)X (Medpydt = dimethyl 2-(di(2-pyridyl)methylene)-1,3-dithiole-4,5-dicarboxylate; X = Cl, 1; X = Br, 2) and Re(CO)3(MebpyTTF)X (MebpyTTF = 4,5-bis(methyloxycabonyl)-4′,5′-(4′-methyl-2,2′-dipyrid-4-ylethylenedithio)-tetrathiafulvalene; X = Cl, 5; X = Br, 6), were prepared from the reactions between Re(CO)5X (X = Cl, Br) and Medpydt or MebpyTTF, respectively. Hydrolysis of the above complexes afforded the analogues with carboxylate derivatives, Re(CO)3(H2dpydt)X (X = Cl, 3; X = Br, 4) and Re(CO)3(H2bpyTTF)X (X = Cl, 7; X = Br, 8). The crystal structures for complexes 1 · 2H2O, 5 and 6 were determined using X-ray single crystal diffraction. UV–Vis absorption spectra of the rhenium complexes show the intraligand and MLCT transitions. Electrochemical behaviors of all new compounds were studied with cyclic voltammetry. Upon irradiation, complexes 3–6 exhibit blue to red emissions in fluid solutions at the room temperature. The performance of complexes 3, 4, 7 and 8 as photosensitizers for anatase TiO2 solar cells was preliminarily investigated as well.