46th Annual Meeting of the APS Division of Atomic, Molecular and Optical Physics
Volume 60, Number 7
Monday–Friday, June 8–12, 2015;
Columbus, Ohio
Session U2: Hot Topics
10:30 AM–12:30 PM,
Friday, June 12, 2015
Room: Union ABC
Chair: David Weiss, Pennsylvania State University
Abstract ID: BAPS.2015.DAMOP.U2.3
Abstract: U2.00003 : Visualizing Au-Au bond formation in solution with femtosecond X-ray scattering
11:30 AM–12:00 PM
Preview Abstract
Abstract
Author:
Shin-ichi Adachi
(Photon Factory, Institute of Materials Structure Science, KEK)
Bond formation is an essential process in chemical reactions, but it is
challenging to keep track of detailed atomic movements associated with bond
formation because of its bimolecular nature. Bond formation in solution
phase has been especially elusive because it is difficult to initiate and
follow such diffusion-limited bimolecular processes with ultrafast time
resolution. In this regard, a Au oligomer complex, [Au(CN)$^{-}_{]n}$,
offers a good model system in which to study the dynamics of bond formation
in solution [,2].Using femtosecond time-resolved X-ray scattering, we
successfully visualized in real time the birth of a gold trimer complex,
[Au(CN)$_{2}^{-}$]$_{3}$, that occurs via photoinduced formation of Au-Au
covalent bonds [3]. The ground state of the trimer has Au atoms that are
weakly bound to each other by aurophilic interaction and aligned in a bent
geometry. Upon photoexcitation, the ground state rapidly converts into the
first excited state where Au-Au covalent bonds are formed among Au atoms
aligned in a linear geometry. Subsequently, the state transforms to a
triplet state in 1.6 ps while accompanying further contraction of Au-Au
bonds by 0.1 {\AA}. Later, the triplet state of the trimer converts to a
tetramer on nanosecond time scale. This work showcases the possibility of
tracking detailed structural changes in solution with sub-ps temporal and
sub-angstrom spatial resolutions, thanks to the advent of X-ray free
electron lasers and the advance of data analysis of time-resolved solution
scattering data.\\[4pt]
[1] Rawashdeh-Omary, M. A., Omary, M. A., Patterson, H. H. {\&} Fackler, J.
P., J. Am. Chem. Soc. 123, 11237--11247 (2001). \\[0pt]
[2] Iwamura, M., Nozaki, K., Takeuchi, S. {\&} Tahara, T., J. Am. Chem. Soc.
135, 538--541 (2013). \\[0pt]
[3] Kim, K. H., Kim, J. G., Nozawa, S., Sato, T., Oang, K. Y., Kim, T. W.,
Ki, H., Jo, J., Park, S., Song, C., Sato, T., Ogawa, K., Togashi, T., Tono,
K., Yabashi, M., Ishikawa, T., Kim, J., Ryoo, R., Kim, J., Ihee, H. {\&}
Adachi, S., Nature, 518, 385-389 (2015).
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2015.DAMOP.U2.3