Photoinduced Electron Transfer, Decarboxylation, and Radical Fragmentation of Cysteine Derivatives:  A Chemically Induced Dynamic Nuclear Polarization Study

1996 ◽  
Vol 118 (12) ◽  
pp. 2882-2891 ◽  
Author(s):  
Martin Goez ◽  
Jaroslaw Rozwadowski ◽  
Bronislaw Marciniak
2013 ◽  
Vol 9 ◽  
pp. 1448-1454
Author(s):  
Martin Goez ◽  
Martin Vogtherr

Electron transfer between the title compounds and their radical cations, which were generated by photoinduced electron transfer from the sulfides to excited 2,4,6-triphenylpyrylium cations, was investigated by time-resolved measurements of chemically induced dynamic nuclear polarization (CIDNP) in acetonitrile. The strongly negative activation entropies provide evidence for an associative–dissociative electron exchange involving dimeric radical cations. Despite this mechanistic complication, the free energies of activation were found to be well reproduced by the Marcus theory of electron transfer, with the activation barrier still dominated by solvent reorganization.


Author(s):  
Olga B. Morozova ◽  
Dmitri Stass ◽  
Alexandra V. Yurkovskaya

Kinetics of electron transfer (ET) from tyrosine (Tyr) to short-lived histidine (His) radicals in peptides of different structures was monitored using time-resolved chemically induced dynamic nuclear polarization (CIDNP) to follow...


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