Wild Duncan A, Winkler Kathrin, Stalke Sebastian, Oum Kawon, Lenzer Thomas
Max-Planck-Institut für biophysikalische Chemie, Abt. Spektroskopie und Photochemische Kinetik (10100), Göttingen, Germany.
Phys Chem Chem Phys. 2006 Jun 7;8(21):2499-505. doi: 10.1039/b601669c. Epub 2006 Apr 28.
The ultrafast internal conversion (IC) dynamics of the carbonyl carotenoid 12'-apo-beta-caroten-12'-al has been investigated in solvents of varying polarity using time-resolved femtosecond transient absorption spectroscopy. The molecules were excited to the S(2) state by a pump beam of either 390 or 470 nm. The subsequent intramolecular dynamics were detected at several probe wavelengths covering the S(0)--> S(2) and S(1)--> S(n) bands. For the S(1)--> S(0) internal conversion process, a remarkably strong acceleration with increasing polarity was found, e.g., lifetimes of tau(1) = 220 ps (n-hexane), 91 ps (tetrahydrofuran) and 8.0 ps (methanol) after excitation at 390 nm. The observation can be rationalized by the formation of a combined S(1)/ICT (intramolecular charge transfer) state in the more polar solvents. The effect is even stronger than the strongest one reported so far in the literature for peridinin. Addition of lithium salts to a solution of 12'-apo-beta-caroten-12'-al in ethanol leads only to small changes of the IC time constant tau(1). In addition, we estimate an upper limit for the time constant tau(2) of the S(2)--> S(1) internal conversion process of 300 fs in all solvents.
利用时间分辨飞秒瞬态吸收光谱,在不同极性的溶剂中研究了羰基类胡萝卜素12'-脱辅基-β-胡萝卜素-12'-醛的超快内转换(IC)动力学。通过390或470nm的泵浦光束将分子激发到S(2)态。在覆盖S(0)→S(2)和S(1)→S(n)能带的几个探测波长处检测随后的分子内动力学。对于S(1)→S(0)内转换过程,发现随着极性增加有显著的加速,例如,在390nm激发后,τ(1)的寿命分别为220ps(正己烷)、91ps(四氢呋喃)和8.0ps(甲醇)。这一观察结果可以通过在极性更强的溶剂中形成组合的S(1)/ICT(分子内电荷转移)态来解释。这种效应甚至比文献中迄今报道的叶绿素蛋白最强的效应还要强。向12'-脱辅基-β-胡萝卜素-12'-醛的乙醇溶液中添加锂盐只会导致IC时间常数τ(1)有微小变化。此外,我们估计在所有溶剂中S(2)→S(1)内转换过程的时间常数τ(2)的上限为300fs。