Hashimoto Hideki, Yanagi Kazuhiro, Yoshizawa Masayuki, Polli Dario, Cerullo Giulio, Lanzani Guglielmo, De Silvestri Sandro, Gardiner Alastair T, Cogdell Richard J
Light and Control, PRESTO/JST and Department of Physics, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan.
Arch Biochem Biophys. 2004 Oct 1;430(1):61-9. doi: 10.1016/j.abb.2004.04.022.
The recent availability of laser pulses with 10-20 fs duration, tunable throughout the visible and near infrared wavelengths, has facilitated the investigation, with unprecedented temporal resolution, into the very early events of energy relaxation in carotenoids [Science 298 (2002) 2395; Synth. Metals 139 (2003) 893]. This has enabled us to clearly demonstrate the existence of an additional intermediate state, Sx, lying between the S2 (1(1)Bu+) and S1 (2(1)Ag-) states. In addition, by applying time-resolved stimulated Raman spectroscopy with femtosecond time resolution, it has also been shown that vibrational relaxation in electronic excited states plays an important role in these interconversions. In this mini-review, we describe briefly the current understanding of Sx and the other intermediate excited states that can be formed by relaxation from S2, mainly focusing attention on the above two topics. Emphasis is also placed on some of the major remaining unsolved issues in carotenoid photochemistry.
最近可获得持续时间为10 - 20飞秒、在整个可见光和近红外波长范围内可调谐的激光脉冲,这使得人们能够以前所未有的时间分辨率研究类胡萝卜素中能量弛豫的早期事件[《科学》298 (2002) 2395;《合成金属》139 (2003) 893]。这使我们能够清楚地证明,在S2 (1(1)Bu+)和S1 (2(1)Ag-)态之间存在一个额外的中间态Sx。此外,通过应用具有飞秒时间分辨率的时间分辨受激拉曼光谱,还表明电子激发态中的振动弛豫在这些相互转换中起着重要作用。在这篇小型综述中,我们简要描述了目前对Sx以及可由S2弛豫形成的其他中间激发态的理解,主要关注上述两个主题。同时也强调了类胡萝卜素光化学中一些主要的尚未解决的问题。