Effect of Relaxation of Intramolecular High-Frequency Vibrational Mode on Nonthermal Electron Transfer Probability. Stochastic Point-Transition Approach

2007 ◽  
Vol 111 (11) ◽  
pp. 4445-4451 ◽  
Author(s):  
Valentina A. Mikhailova ◽  
Anatoly I. Ivanov
1999 ◽  
Vol 19 (1-4) ◽  
pp. 385-387
Author(s):  
Chengfei Wang ◽  
Boris Akhremitchev ◽  
Gilbert C. Walker

We present charge transfer absorption, resonance Raman and time-resolved infrared spectral data for (CN)5FeCNRu(NH3)5− in various solvents. The transient infrared spectra and anisotropies reveal both non-equilibrium vibrational populations of high frequency modes and local solvent heating.


Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1326 ◽  
Author(s):  
Noura Zamzam ◽  
Jasper van Thor

We present ground and excited state frequency calculations of the recently discovered extremely red-shifted chlorophyll f. We discuss the experimentally available vibrational mode assignments of chlorophyll f and chlorophyll a which are characterised by particularly large downshifts of 131-keto mode in the excited state. The accuracy of excited state frequencies and their displacements are evaluated by the construction of Franck–Condon (FC) and Herzberg–Teller (HT) progressions at the CAM-B3LYP/6-31G(d) level. Results show that while CAM-B3LYP results are improved relative to B3LYP calculations, the displacements and downshifts of high-frequency modes are underestimated still, and that the progressions calculated for low temperature are dominated by low-frequency modes rather than fingerprint modes that are Resonant Raman active.


1997 ◽  
Vol 70 (18) ◽  
pp. 2452-2454 ◽  
Author(s):  
N. Evers ◽  
J. Laskar ◽  
N. M. Jokerst ◽  
T. S. Moise ◽  
Y.-C. Kao

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