화학공학소재연구정보센터
Inorganic Chemistry, Vol.59, No.20, 14654-14665, 2020
Excitation-Wavelength-Dependent and Auxiliary-Ligand-Tuned Intersystem-Crossing Efficiency in Cyclometalated Platinum(II) Complexes: Spectroscopic and Theoretical Studies
Understanding the factors affecting the intersystem-crossing (ISC) rate constant (k(ISC)) of transition-metal complexes is crucial to material design with tailored photophysical properties. Most of the works on ISC to date focused on the influence by the chromophoric ligand and the understanding of the ISC efficiency were mainly drawn from the steady-state fluorescence to phosphorescence intensity ratio and ground-state calculations, with only a few high-level calculations on k(ISC) that take excited-state structural change and solvent reorganization into account for quantitative comparisons with the experimental data. In this work, a series of [Pt(thpy)X)](+) complexes were prepared [Hthpy = 2-(2'-thienyl)pyridine, where X = auxiliary ligands] and characterized by both steady-state and time-resolved luminescence spectroscopies. A panel of auxiliary ligands with varying sigma-donating/ pi-accepting character have been used. For comparison, analogues of [Pt(ppy)((PP)-P-boolean AND)](+) (Hppy = 2-phenylpyridine and (PP)-P-boolean AND = diphosphino ligand) were also examined. The [Pt(thpy)((PP)-P-boolean AND)](+) complexes exhibit dual fluorescence-phosphorescence emission, with their ISC rate constants varied with the electronic characteristics of the auxiliary ligand: the more electron-donating ligand induces faster ISC from the S-1 excited state to the triplet manifold. Density functional theory (DFT)/time-dependent DFT calculations of k(ISC) (S-1 -> T-2) at the optimized excited-state geometries give excellent quantitative agreement with the femtosecond time-resolved fluorescence measurements; it was revealed that the more electron-donating auxiliary ligand increases metal contributions to both occupied and virtual orbitals and decreases the energy gap of the coupling excited states, leading to a decrease in the activation energy and an increase in spin-orbit coupling. Furthermore, the ISC rate constants of [Pt(thpy)((PP)-P-boolean AND)](+) complexes are found to depend on the excitation wavelengths. The deviation from Kasha-Vavilov's rule upon photoexcitation at lambda(exc) < 350 nm is due to the ultrafast S-2 -> T-2 and S-2 -> T-3 ISCs, as demonstrated by the calculated tau(ISC) < 100 fs, giving hints as to why S-2 -> S-1 internal conversion (tau(IC) similar to ps ) is not competitive with this hyper-ISC.