Excited State Dynamics and Activation Parameters of Remarkably Slow Photoinduced CO Loss from (η6-Benzene)Cr(CO)3inn-Heptane Solution: A DFT and Picosecond-Time-Resolved Infrared Study

2010 ◽  
Vol 114 (43) ◽  
pp. 11425-11431 ◽  
Author(s):  
Ian P. Clark ◽  
Michael W. George ◽  
Gregory M. Greetham ◽  
Emma C. Harvey ◽  
Conor Long ◽  
...  
2019 ◽  
Vol 10 (1) ◽  
pp. 134-144 ◽  
Author(s):  
Monica C. Carey ◽  
Sara L. Adelman ◽  
James K. McCusker

In order to better define the nature of the nuclear coordinate associated with excited state dynamics in first-row transition metal chromophores, variable-temperature ultrafast time-resolved absorption spectroscopy has been used to determine activation parameters associated with ground state recovery in a series of low-spin Fe(ii) polypyridyl complexes.


2015 ◽  
Vol 17 (47) ◽  
pp. 31978-31987 ◽  
Author(s):  
Franziska Buchner ◽  
Berit Heggen ◽  
Hans-Hermann Ritze ◽  
Walter Thiel ◽  
Andrea Lübcke

Time-resolved photoelectron spectroscopy is performed on aqueous guanosine solution to study its excited-state relaxation dynamics.


2020 ◽  
Vol 11 (20) ◽  
pp. 5191-5204 ◽  
Author(s):  
Jennifer N. Miller ◽  
James K. McCusker

Time-resolved spectroscopic measurements of ground-state recovery for [Fe(bpy)3]2+ reveal that the solvent can induce an outer-sphere reorganization energy effect on excited-state dynamics involving metal-centered ligand-field electronic states.


2004 ◽  
Vol 121 (19) ◽  
pp. 9436-9442 ◽  
Author(s):  
Chie Okabe ◽  
Takakazu Nakabayashi ◽  
Yoshiya Inokuchi ◽  
Nobuyuki Nishi ◽  
Hiroshi Sekiya

2019 ◽  
Vol 205 ◽  
pp. 05014 ◽  
Author(s):  
Roseanne J. Sension ◽  
Nicholas A. Miller ◽  
Aniruddha Deb ◽  
Roberto Alonso-Mori ◽  
James M. Glownia ◽  
...  

Polarized time-resolved X-ray absorption near edge structure (XANES) is used to characterize the sequential ballistic excited state dynamics of two B12 vitamers: cyanocobalamin and adenosylcobalamin. Excitation at 550 nm and 365 nm is used to resolve axial and equatorial contributions to the excited state dynamics.


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