scholarly journals Filming ultrafast roaming-mediated isomerization of bismuth triiodide in solution

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Eun Hyuk Choi ◽  
Jong Goo Kim ◽  
Jungmin Kim ◽  
Hosung Ki ◽  
Yunbeom Lee ◽  
...  

AbstractRoaming reaction, defined as a reaction yielding products via reorientational motion in the long-range region (3 – 8 Å) of the potential, is a relatively recently proposed reaction pathway and is now regarded as a universal mechanism that can explain the unimolecular dissociation and isomerization of various molecules. The structural movements of the partially dissociated fragments originating from the frustrated bond fission at the onset of roaming, however, have been explored mostly via theoretical simulations and rarely observed experimentally. Here, we report an investigation of the structural dynamics during a roaming-mediated isomerization reaction of bismuth triiodide (BiI3) in acetonitrile solution using femtosecond time-resolved x-ray liquidography. Structural analysis of the data visualizes the atomic movements during the roaming-mediated isomerization process including the opening of the Bi-Ib-Ic angle and the closing of Ia-Bi-Ib-Ic dihedral angle, each by ~40°, as well as the shortening of the Ib···Ic distance, following the frustrated bond fission.

2004 ◽  
Author(s):  
Kazutaka G. Nakamura ◽  
Hiroaki Kishimura ◽  
Yoichiro Hironaka ◽  
Ken-ichi Kondo

Author(s):  
A. H. Chin ◽  
R. W. Schoenlein ◽  
T. E. Glover ◽  
P. Balling ◽  
W. P. Leemans ◽  
...  

Author(s):  
Matthew R. Ross ◽  
Benjamin E Van Kuiken ◽  
Matthew L. Strader ◽  
Hana Cho ◽  
Amy Cordones-Hahn ◽  
...  

1999 ◽  
Vol 83 (2) ◽  
pp. 336-339 ◽  
Author(s):  
A. H. Chin ◽  
R. W. Schoenlein ◽  
T. E. Glover ◽  
P. Balling ◽  
W. P. Leemans ◽  
...  

Author(s):  
Majed Chergui

The need to visualize molecular structure in the course of a chemical reaction, a phase transformation or a biological function has been a dream of scientists for decades. The development of time-resolved X-ray and electron-based methods is making this true. X-ray absorption spectroscopy is ideal for the study of structural dynamics in liquids, because it can be implemented in amorphous media. Furthermore, it is chemically selective. Using X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) in laser pump/X-ray probe experiments allows the retrieval of the local geometric structure of the system under study, but also the underlying photoinduced electronic structure changes that drive the structural dynamics. Recent developments in picosecond and femtosecond X-ray absorption spectroscopy applied to molecular systems in solution are reviewed: examples on ultrafast photoinduced processes such as intramolecular electron transfer, low-to-high spin change, and bond formation are presented.


2002 ◽  
Vol 116 (7) ◽  
pp. 2955-2966 ◽  
Author(s):  
Christian Bressler ◽  
Melanie Saes ◽  
Majed Chergui ◽  
Daniel Grolimund ◽  
Rafael Abela ◽  
...  

2016 ◽  
Vol 3 (2) ◽  
pp. 023610 ◽  
Author(s):  
Jong Goo Kim ◽  
Srinivasan Muniyappan ◽  
Key Young Oang ◽  
Tae Wu Kim ◽  
Cheolhee Yang ◽  
...  

2021 ◽  
Author(s):  
Yuushi Shimoda ◽  
Kiyoshi Miyata ◽  
Masataka Funaki ◽  
Tatsuki Morimoto ◽  
Shunsuke Nozawa ◽  
...  

We have explored the structural factors on the photophysical properties in two rhenium(I) diimine complexes in acetonitrile solution, cis,trans-[Re(dmb)(CO)<sub>2</sub>(PPh<sub>2</sub>Et)<sub>2</sub>]+ (Et(2,2)) and cis,trans-[Re(dmb)(CO)<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>]+ ((3,3)) (dmb = 4,4'-dimethyl-2,2'-bipyridine, Ph = phenyl, Et = ethyl) using the combination method of time-resolved infrared spectroscopy, time-resolved extended X-ray absorption fine structure, and quantum chemical calculations. The difference between these complexes is the number of phenyl groups in the phosphine ligand, and this only indirectly affects the central Re(I). Despite this minor difference, the complexes exhibit large differences in emission wavelength and excited-state lifetime. Upon photoexcitation, the bond length of Re-P and angle of P-Re-P are significantly changed in both complexes, while the phenyl groups are largely rotated by ~20º only in (3,3). We concluded that the instability from steric effects of phenyl groups and diimine leads to the smaller Stokes shift of the lowest excited triplet state (T<sub>1</sub>) in (3,3). The large structural change between the ground and excited states causes the longer lifetime of T<sub>1</sub> in (3,3).


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