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利用飞秒 X 射线散射直接观察溶液中键的形成。

Direct observation of bond formation in solution with femtosecond X-ray scattering.

机构信息

1] Center for Nanomaterials and Chemical Reactions, Institute for Basic Science, Daejeon 305-701, South Korea [2] Department of Chemistry, KAIST, Daejeon 305-701, South Korea.

Institute of Materials Structure Science, High Energy Accelerator Research Organization, 1-1 Oho, Tsukuba, Ibaraki 305-0801, Japan.

出版信息

Nature. 2015 Feb 19;518(7539):385-9. doi: 10.1038/nature14163.

DOI:10.1038/nature14163
PMID:25693570
Abstract

The making and breaking of atomic bonds are essential processes in chemical reactions. Although the ultrafast dynamics of bond breaking have been studied intensively using time-resolved techniques, it is very difficult to study the structural dynamics of bond making, mainly because of its bimolecular nature. It is especially difficult to initiate and follow diffusion-limited bond formation in solution with ultrahigh time resolution. Here we use femtosecond time-resolved X-ray solution scattering to visualize the formation of a gold trimer complex, [Au(CN)2(-)]3 in real time without the limitation imposed by slow diffusion. This photoexcited gold trimer, which has weakly bound gold atoms in the ground state, undergoes a sequence of structural changes, and our experiments probe the dynamics of individual reaction steps, including covalent bond formation, the bent-to-linear transition, bond contraction and tetramer formation with a time resolution of ∼500 femtoseconds. We also determined the three-dimensional structures of reaction intermediates with sub-ångström spatial resolution. This work demonstrates that it is possible to track in detail and in real time the structural changes that occur during a chemical reaction in solution using X-ray free-electron lasers and advanced analysis of time-resolved solution scattering data.

摘要

原子键的形成和断裂是化学反应中的基本过程。虽然使用时间分辨技术已经对键断裂的超快动力学进行了深入研究,但研究键形成的结构动力学非常困难,主要是因为它的双分子性质。特别是在超高速分辨率下,在溶液中引发和跟踪扩散限制的键形成非常困难。在这里,我们使用飞秒时间分辨 X 射线溶液散射技术实时可视化金三聚体复合物[Au(CN)2(-)]3 的形成,而不受缓慢扩散的限制。这种光激发的金三聚体在基态下具有结合较弱的金原子,经历了一系列结构变化,我们的实验探测了包括共价键形成、弯曲到线性转变、键收缩和四聚体形成在内的各个反应步骤的动力学,时间分辨率约为 500 飞秒。我们还以亚埃的空间分辨率确定了反应中间体的三维结构。这项工作表明,使用 X 射线自由电子激光和对时间分辨溶液散射数据的高级分析,有可能详细实时地跟踪溶液中化学反应过程中发生的结构变化。

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