Kim Jeongho, Kim Kyung Hwan, Oang Key Young, Lee Jae Hyuk, Hong Kiryong, Cho Hana, Huse Nils, Schoenlein Robert W, Kim Tae Kyu, Ihee Hyotcherl
Department of Chemistry, Inha University, Incheon 402-751, Republic of Korea.
Center for Nanomaterials and Chemical Reactions, Institute for Basic Science, Daejeon, 305-701, Republic of Korea.
Chem Commun (Camb). 2016 Mar 7;52(19):3734-49. doi: 10.1039/c5cc08949b.
Characterization of transient molecular structures formed during chemical and biological processes is essential for understanding their mechanisms and functions. Over the last decade, time-resolved X-ray liquidography (TRXL) and time-resolved X-ray absorption spectroscopy (TRXAS) have emerged as powerful techniques for molecular and electronic structural analysis of photoinduced reactions in the solution phase. Both techniques make use of a pump-probe scheme that consists of (1) an optical pump pulse to initiate a photoinduced process and (2) an X-ray probe pulse to monitor changes in the molecular structure as a function of time delay between pump and probe pulses. TRXL is sensitive to changes in the global molecular structure and therefore can be used to elucidate structural changes of reacting solute molecules as well as the collective response of solvent molecules. On the other hand, TRXAS can be used to probe changes in both local geometrical and electronic structures of specific X-ray-absorbing atoms due to the element-specific nature of core-level transitions. These techniques are complementary to each other and a combination of the two methods will enhance the capability of accurately obtaining structural changes induced by photoexcitation. Here we review the principles of TRXL and TRXAS and present recent application examples of the two methods for studying chemical and biological processes in solution. Furthermore, we briefly discuss the prospect of using X-ray free electron lasers for the two techniques, which will allow us to keep track of structural dynamics on femtosecond time scales in various solution-phase molecular reactions.
表征化学和生物过程中形成的瞬态分子结构对于理解其机制和功能至关重要。在过去十年中,时间分辨X射线液体成像(TRXL)和时间分辨X射线吸收光谱(TRXAS)已成为用于溶液相中光诱导反应的分子和电子结构分析的强大技术。这两种技术都采用泵浦-探测方案,该方案包括:(1)一个光泵浦脉冲来引发光诱导过程;(2)一个X射线探测脉冲来监测分子结构随泵浦脉冲和探测脉冲之间时间延迟的变化。TRXL对整体分子结构的变化敏感,因此可用于阐明反应溶质分子的结构变化以及溶剂分子的集体响应。另一方面,由于芯能级跃迁的元素特异性,TRXAS可用于探测特定X射线吸收原子的局部几何结构和电子结构的变化。这些技术相互补充,两种方法的结合将增强准确获取光激发引起的结构变化的能力。在这里,我们回顾了TRXL和TRXAS的原理,并展示了这两种方法在研究溶液中的化学和生物过程方面的最新应用实例。此外,我们简要讨论了将X射线自由电子激光用于这两种技术的前景,这将使我们能够在各种溶液相分子反应中跟踪飞秒时间尺度上的结构动力学。