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

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.

Graphical abstractRhenium(I) tricarbonyl complexes with bispyridine ligands incorporating with delocalized sulfur-rich units, Re(CO)3(Medpydt)X and Re(CO)3(MebpyTTF)X, have been prepared. Hydrolysis of the above complexes affords the analogue products with carboxylate derivatives. Complexes 3–6 exhibit blue to red emissions. The performance of some typical complexes as photosensitizers for anatase TiO2 solar cells has been preliminarily investigated.Figure optionsDownload full-size imageDownload as PowerPoint slide