摘要

A rhenium(I) tricarbonyl complex, [Re(CO)(3)(IDIMPhen)Cl] (IDIMPhen-Re) [where IDIMPhen = 2-(3-indolyl)-imidazo[4,5-f]-[1,10] phenanthroline], have been successfully synthesized and fully characterized by H-1 NMR, C-13 NMR, IR, GC-MS, elemental analysis, UV-Vis and cyclic voltammetry (CV). Meanwhile, the electronic structure and spectroscopic features of IDIMPhen-Re have been investigated using the density functional theory (DFT) and time-dependent DFT methods. Based on the calculated results, the experiment data are explained in great detail. The calculated orbital energies of the HOMO and LUMO of IDIMPhen-Re are in reasonable agreement with those obtained from the electrochemical measurements. The lowest lying singlet -> singlet absorption band of IDIMPhen-Re, corresponding to the prominent absorption peak at 447 nm observed in experiments, should be assigned to the pure HOMO -> LUMO transition. The calculated IP and EA show that IDIMPhen-Re possesses the good hole-transfer ability and the balanced transport of electrons and holes is more accessible compared with its analogue Phen-Re.