Formation of a long-lived radical pair in a Sn(iv) porphyrin–di(l-tyrosinato) conjugate driven by proton-coupled electron-transfer

2018 ◽  
Vol 54 (48) ◽  
pp. 6148-6152 ◽  
Author(s):  
Mirco Natali ◽  
Agnese Amati ◽  
Nicola Demitri ◽  
Elisabetta Iengo

A surprisingly long-lived radical pair state is achieved in a tin-porphyrin/l-tyrosine conjugate by exploiting a photochemical PCET quenching mechanism.

2003 ◽  
Vol 81 (6) ◽  
pp. 789-798 ◽  
Author(s):  
Guilford Jones II ◽  
Xiaochun Wang ◽  
Jingqiu Hu

The electron-transfer photochemistry of rhodamine 6G thiocyanate ion pairs has been investigated. For dye in a low polarity solvent, such as ethyl acetate, the emission of rhodamine 6G is significantly quenched by thiocyanate counterions. Laser photolysis of rhodamine 6G and thiocyanate in ethyl acetate was studied in detail with the identification of the reduced rhodamine 6G radical species (λmax = 410 nm). The growth and decay of the R6G radical could be accounted for in part by a mechanism involving initial formation of dye triplet followed by electron transfer which provides a triplet radical-pair state on a µs timescale.Key words: electron transfer, ion pair, rhodamine 6G, triplet state.


2017 ◽  
Vol 231 (2) ◽  
Author(s):  
Prashanth K. Poddutoori ◽  
Yuri E. Kandrashkin ◽  
Art van der Est

AbstractThe stabilization of light-induced charge separation in two axially bound triads based on aluminum(III) porphyrin (AlPor) are investigated using the electron spin polarization patterns of the final radical pair state. In the triads, TTF-(Ph)


2021 ◽  
Vol 143 (8) ◽  
pp. 3104-3112
Author(s):  
Yusuke Yoneda ◽  
S. Jimena Mora ◽  
James Shee ◽  
Brian L. Wadsworth ◽  
Eric A. Arsenault ◽  
...  

2021 ◽  
Author(s):  
Anthony Wong ◽  
Arunavo Chakraborty ◽  
Deependra Bawari ◽  
Guang Wu ◽  
Roman Dobrovetsky ◽  
...  

Coordination induced bond weakening (CIBW) leads to facile PCET at various E–H bonds.


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