Hsu Feng-Cheng, Hayashi Michitoshi, Wang Houng-Wei, Lin Sheng Hsien, Wang Juen-Kai
Department of Chemistry, National Taiwan University, Taipei, Taiwan 106.
J Phys Chem A. 2007 Feb 8;111(5):759-63. doi: 10.1021/jp0652897.
We report a study of excited-state dynamics of trans,trans-distyrylbenzene in hexane solution with femtosecond two-color transient absorption spectroscopy. A consistent model of two distinct excited states, S1 and X, connected by the 10 ps dynamics is proposed with the support from the analysis of excited-state anisotropy. An investigation on the 10 ps dynamics with varying excitation energy has been also conducted. In the assumption of fast intramolecular vibrational redistribution, a dependence of this nonradiative 10 ps process on intramolecular temperature in the S1 state has been analyzed. We have found that an effective mode of approximately 1270 cm-1 is responsible for the 10 ps dynamics. The analysis of both anisotropy and pump-dependent results further implies that a distribution of rotamers may exist in the X state. The result indicates a drastic different excited-state relaxation pathway than that of trans-stilbene.
我们报道了一项利用飞秒双色瞬态吸收光谱对反式、反式二苯乙烯基苯在己烷溶液中的激发态动力学进行的研究。在激发态各向异性分析的支持下,提出了一个由10皮秒动力学连接的两个不同激发态S1和X的一致模型。还对不同激发能量下的10皮秒动力学进行了研究。在快速分子内振动重新分布的假设下,分析了这种非辐射10皮秒过程对S1态分子内温度的依赖性。我们发现,约1270厘米-1的一个有效模式是10皮秒动力学的原因。对各向异性和泵浦依赖结果的分析进一步表明,X态中可能存在旋转异构体分布。结果表明,其激发态弛豫途径与反式芪截然不同。