Kim JunWoo, Kang Dong-Gu, Kim Sang Kyu, Joo Taiha
Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
Phys Chem Chem Phys. 2020 Nov 18;22(44):25811-25818. doi: 10.1039/d0cp05368f.
Ultrafast intersystem crossing (ISC) in transition metal complexes leads to a long-lived active state with a high yield, which leads to efficient light energy conversion. The detailed mechanism of ISC may lead to a rational molecular design of superior transition metal complexes. Coherent nuclear wave packets observed in femtosecond time-resolved spectroscopies provide important information on the excited-state dynamics. In particular, analyzing the nuclear wave packets in both the reactant and the product may unveil the molecular dynamics of an ultrafast reaction. In this study, experimental evidence proving the reaction coordinates of the ultrafast ISC of ruthenium(ii) complexes is presented using coherent vibrational spectroscopy with a quantum chemical simulation of coherent vibrational motion. We observed vibrational modes strongly coupled to the ISC, whose vibrational coherences undergo remarkable attenuation after the ISC. The coupled modes contain metal-ligand stretching or symmetry breaking components, and the faster ISC rates of lower-symmetry ruthenium(ii) complexes support the significance of the latter.
过渡金属配合物中的超快系间窜越(ISC)会产生高产率的长寿命活性态,从而实现高效的光能转换。ISC的详细机制可能会促成对优质过渡金属配合物进行合理的分子设计。在飞秒时间分辨光谱中观察到的相干核波包提供了有关激发态动力学的重要信息。特别是,分析反应物和产物中的核波包可能会揭示超快反应的分子动力学。在本研究中,我们利用相干振动光谱并结合相干振动运动的量子化学模拟,给出了证明钌(II)配合物超快ISC反应坐标的实验证据。我们观察到与ISC强烈耦合的振动模式,其振动相干性在ISC之后会经历显著衰减。耦合模式包含金属-配体拉伸或对称性破缺成分,并且低对称性钌(II)配合物更快的ISC速率支持了后者的重要性。