Theoretical studies on the electronic structure and spectral properties of versatile diarylethene-containing 1,10-phenanthroline ligands and their rhenium(I) complexes

The structures of versatile diarylethene-containing 1,10-phenanthroline ligands (L1 and L2) and their rhenium(I) complexes [Re(CO)3(L)Cl] (1 and 2) in the ground and low-lying excited states have been optimized at the B3LYP functional and the ab initio configuration interaction singlets (CIS) level, respectively. The spectral properties are predicted with use of time-dependent density functional theory (TDDFT). As shown, the transition character of the strongest absorption band and luminescent spectrum for closed-ring complex 1 is different from that of 2, the former has ππ∗ character and the latter has MLCT and LLCT character. We presume the second triplet excited state contributes to the phosphorescence of 1, while the lowest triplet excited state accounts for the phosphorescence of 2. Spin–orbit coupling influences the excitation energies for d(Re)-joined transitions whereas it has negligible effect on the transition character for complexes 1 and 2.

A DFT/TDDFT study on versatile diarylethene-containing 1,10-phenanthroline ligands (L1 and L2) and their rhenium(I) complexes [Re(CO)3(L)Cl] (1 and 2) has been carried out. The electronic structures and spectral properties of these systems were theoretically explained.Figure optionsDownload as PowerPoint slide