Theoretical Studies on Structures and Spectroscopic Properties of Cyclometalated Gold(III) Complexes

Abstract

The electronic structures and spectroscopic properties of the four tridentate cyclometalated Au(III) complexes [Au(ĈN̂C)C≡CPh] (1), [Au(N̂ĈC)C≡CPh] (2), [Au(N̂N̂C)C≡CPh]+ (3), and [Au(N̂ĈN)C≡CPh]+ (4) [HĈN̂CH = 2,6 -diphenylpyridine, N̂CĤCH = 3-(2-pyridyl)biphenyl, N̂N̂CH = 6-phenyl-2,2′- bipyridine, N̂CHN̂ = 1,3-di(2-pyridyl)benzene] were calculated to explore their spectroscopic nature. The geometry structures of 1−4 in the ground and excited states were optimized under the density functional theory (DFT) and the single-excitation configuration interaction (CIS) level, respectively. The absorption and emission spectra in CH2Cl2 solution were calculated by the time-dependent density functional theory (TD-DFT) with the PCM solvent model. As revealed from the calculations, with the variation of pyridyl in position and the number, the electron-accepting ability of pyridyl in 1−4 are different. With increasing the electron-accepting ability of pyridyl, the HOMO−LUMO energy gaps of 1−4 decrease, and the lowest-energy absorption bands and emission bands are red-shifted in the order 1 2 4 3. All of the lowest-energy absorptions are assigned as the LLCT character, and the solvent polarity has little impact on the absorption spectra. The 477 nm emission of 1 arises from the 3ILCT transition, whereas the 517 and 634 nm emission of 2 and 3, respectively, come from the 3LLCT and 3ILCT. In addition, the 577 nm emission of 4 is assigned as 3LLCT/3LMCT character