| Literature DB >> 25693570 |
Kyung Hwan Kim1, Jong Goo Kim1, Shunsuke Nozawa2, Tokushi Sato2, Key Young Oang1, Tae Wu Kim1, Hosung Ki1, Junbeom Jo1, Sungjun Park1, Changyong Song3, Takahiro Sato3, Kanade Ogawa3, Tadashi Togashi4, Kensuke Tono4, Makina Yabashi3, Tetsuya Ishikawa3, Joonghan Kim5, Ryong Ryoo1, Jeongho Kim6, Hyotcherl Ihee1, Shin-ichi Adachi7.
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.Year: 2015 PMID: 25693570 DOI: 10.1038/nature14163
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962