Ultrafast Electron Transfer Dynamics in Ruthenium Polypyridyl Complexes with a π-Conjugated Ligand†

2010 ◽  
Vol 114 (45) ◽  
pp. 14679-14688 ◽  
Author(s):  
Joseph D. Henrich ◽  
Haoyu Zhang ◽  
Prabir K. Dutta ◽  
Bern Kohler
2020 ◽  
Vol 11 (32) ◽  
pp. 8600-8609 ◽  
Author(s):  
Páraic M. Keane ◽  
Kyra O'Sullivan ◽  
Fergus E. Poynton ◽  
Bjørn C. Poulsen ◽  
Igor V. Sazanovich ◽  
...  

Efficient electron transfer requires the complex to be intercalated at a G-C base-pair. Identification of preferred intercalation sites is achieved by TRIR monitoring of the nucleobase vibrations before electron transfer.


2010 ◽  
Vol 16 (9) ◽  
pp. 2830-2842 ◽  
Author(s):  
Rohan J. Kumar ◽  
Susanne Karlsson ◽  
Daniel Streich ◽  
Alice Rolandini Jensen ◽  
Michael Jäger ◽  
...  

1999 ◽  
Vol 38 (26) ◽  
pp. 6320-6322 ◽  
Author(s):  
Yuan-jun Hou ◽  
Pu-hui Xie ◽  
Bao-wen Zhang ◽  
Yi Cao ◽  
Xu-rui Xiao ◽  
...  

2003 ◽  
Vol 68 (8) ◽  
pp. 1467-1487 ◽  
Author(s):  
Wesley R. Browne ◽  
Frances Weldon ◽  
Adrian Guckian ◽  
Johannes G. Vos

The syntheses and characterisation of a series of mononuclear and dinuclear ruthenium polypyridyl complexes based on the bridging ligands 1,3-bis-[5-(2-pyridyl)-1H-1,2,4-triazol-3-yl]benzene, 1,4-bis-[5-(2-pyridyl)-1H-1,2,4-triazol-3-yl]benzene, 2,5-bis-[5-(2-pyridyl)-1H-1,2,4-triazol-3-yl]thiophene, 2,5-bis-[5-pyrazinyl-1H-1,2,4-triazol-3-yl]thiophene are reported. Electrochemical studies indicate that in these systems, the ground state interaction is critically dependent on the nature of the bridging ligand and its protonation state, with strong and weak interactions being observed for thiophene- and phenylene-bridged complexes, respectively.


2018 ◽  
Vol 190 ◽  
pp. 03012
Author(s):  
Charles W. Stark ◽  
M. Rammo ◽  
K. Petritšenko ◽  
J. Pahapill ◽  
A. Mikhaylov ◽  
...  

Quantitative two-photon absorption (2PA) cross section and 2PA spectrum measurements were used to determine the molecular electric dipole change in the metal-to-ligand charge-transfer transition of ruthenium(II) tris-complexes of 2,2’-bipyridine ([Ru(bpy)3]2+) and 1,10-phenanthroline ([Ru(phen)3]2+) in several solvents.


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