Houk Amanda L, Zheldakov Igor L, Tommey Tyler A, Elles Christopher G
Department of Chemistry, University of Kansas, Lawrence, Kansas 66045, United States.
J Phys Chem B. 2015 Jul 23;119(29):9335-44. doi: 10.1021/jp509959n. Epub 2014 Nov 10.
The photoisomerization dynamics of trans-stilbene have been well studied in the lowest excited state, but much less is known about the behavior following excitation to higher-lying electronically excited states. This contribution reports a combined study of the spectroscopy and dynamics of two-photon accessible states above S1. Two-photon absorption (2PA) measurements using a broadband pump-probe technique reveal distinct bands near 5.1 and 6.4 eV. The 2PA bands have absolute cross sections of 40 ± 16 and 270 ± 110 GM, respectively, and a pump-probe polarization dependence that suggests both of the transitions access Ag-symmetry excited states. Separate transient absorption measurements probe the excited-state dynamics following two-photon excitation into each of the bands using intense pulses of 475 and 380 nm light, respectively. The initially excited states rapidly relax via internal conversion, leading to the formation of an S1 excited-state absorption band that is centered near 585 nm and evolves on a time scale of 1-2 ps due to intramolecular vibrational relaxation. The subsequent evolution of the S1 excited-state absorption is identical to the behavior following direct one-photon excitation of the lowest excited state at 4.0 eV. The complementary spectroscopy and dynamics measurements provide new benchmarks for computational studies of the electronic structure and dynamics of this model system on excited states above S1. Probing the dynamics of molecules in their higher-lying excited states is an important frontier in chemical reaction dynamics.
反式芪的光异构化动力学在最低激发态已得到充分研究,但对于激发到更高电子激发态后的行为了解较少。本文报道了对S1以上双光子可及态的光谱学和动力学的联合研究。使用宽带泵浦 - 探测技术进行的双光子吸收(2PA)测量揭示了在5.1和6.4 eV附近的不同谱带。这两个2PA谱带的绝对截面分别为40±16和270±110 GM,并且泵浦 - 探测偏振依赖性表明这两个跃迁均通向Ag对称激发态。分别进行的瞬态吸收测量使用475和380 nm的强脉冲光探测双光子激发到每个谱带后的激发态动力学。初始激发态通过内转换迅速弛豫,导致形成一个以585 nm附近为中心的S1激发态吸收带,并且由于分子内振动弛豫,该吸收带在1 - 2 ps的时间尺度上演变。S1激发态吸收的后续演变与在4.0 eV处直接单光子激发最低激发态后的行为相同。互补的光谱学和动力学测量为该模型系统在S1以上激发态的电子结构和动力学的计算研究提供了新的基准。探测分子在其更高激发态的动力学是化学反应动力学中的一个重要前沿领域。