Effects of Pressure on the Thermal Back Electron Transfer in a Dibenzylbipyridinium Salt. Solvent Reorganizations and Dynamic Solvent Effects

2004 ◽  
Vol 33 (12) ◽  
pp. 1542-1543 ◽  
Author(s):  
Mehdi S. Shihab ◽  
Koji Kubota ◽  
Toru Takahashi ◽  
Yasushi Ohga ◽  
Tsutomu Asano
1988 ◽  
Vol 66 (2) ◽  
pp. 319-324 ◽  
Author(s):  
R. J. DeVoe ◽  
M. R. V. Sahyun ◽  
Einhard Schmidt ◽  
N. Serpone ◽  
D. K. Sharma

We have studied the anthracene-sensitized photolyses of both diphenyliodonium and triphenylsulphonium salts in solution using both steady-state and laser flash photolysis techniques. Photoproducts, namely, phenylated anthracenes along with iodobenzene or diphenylsulphide, respectively, are obtained from both salts with quantum efficiencies of ca. 0.1 at 375 nm. We infer the intermediacy of diphenyliodo and triphenylsulphur radicals formed by single electron transfer from the singlet-excited anthracene. We have developed a quantitative model of this chemistry, and identify the principal sources of inefficiency as back electron transfer, which occurs at nearly the theoretically limiting rate, intersystem crossing from the initially formed sensitizer–'onium salt encounter complex, and in-cage radical recombination.


2017 ◽  
Vol 19 (22) ◽  
pp. 14412-14423 ◽  
Author(s):  
Ewelina Krzyszkowska ◽  
Justyna Walkowiak-Kulikowska ◽  
Sven Stienen ◽  
Aleksandra Wojcik

Quenching of the thionine singlet excited state in covalently functionalized graphene oxide with an efficient back electron transfer process.


2017 ◽  
Vol 9 (39) ◽  
pp. 33887-33895 ◽  
Author(s):  
Heng Zhu ◽  
Shicheng Yan ◽  
Zhaosheng Li ◽  
Zhigang Zou

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