Adams Bethany S, Shillito Georgina E, van der Salm Holly, Horvath Raphael, Larsen Christopher B, Sun Xue-Zhong, Lucas Nigel T, George Michael W, Gordon Keith C
School of Chemistry, University of Nottingham , University Park, Nottingham NG7 2RD, U.K.
Department of Chemistry, University of Otago , P.O. Box 56, Dunedin, New Zealand.
Inorg Chem. 2017 Nov 6;56(21):12967-12977. doi: 10.1021/acs.inorgchem.7b01710. Epub 2017 Oct 6.
The ground- and excited-state properties of a series of [ReCl(CO)(dppz)] complexes with substituted donor groups were investigated. Alteration of donor-acceptor communication through modulation of torsional angle and the number and nature of the donor substituents allowed the effects on the photophysical properties to be characterized though both computational and spectroscopic techniques, including time-dependent density functional theory and resonance Raman and time-resolved infrared spectroscopy. The ground-state optical properties show significant variation as a result of donor group modulation, with an increased angle between the donor and acceptor blue-shifting and depleting the intensity of the lowest-energy transition, which is consistently intraligand charge transfer (ILCT) in nature. However, across all complexes studied there was minimal perturbation to the excited-state properties and dynamics. Three excited states on the picosecond, nanosecond, and microsecond time scales were observed in all cases, corresponding to ILCT, ππ*, and ILCT, respectively.
研究了一系列带有取代供体基团的[ReCl(CO)(dppz)]配合物的基态和激发态性质。通过扭转角以及供体取代基的数量和性质的调制来改变供体-受体相互作用,从而能够通过计算和光谱技术(包括含时密度泛函理论、共振拉曼光谱和时间分辨红外光谱)来表征对光物理性质的影响。由于供体基团的调制,基态光学性质显示出显著变化,供体与受体之间角度的增加导致蓝移并降低了最低能量跃迁的强度,该跃迁本质上始终是配体内电荷转移(ILCT)。然而,在所研究的所有配合物中,激发态性质和动力学受到的扰动最小。在所有情况下均观察到皮秒、纳秒和微秒时间尺度上的三个激发态,分别对应于ILCT、ππ*和ILCT。