Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9575255 | Chemical Physics | 2005 | 9 Pages |
Abstract
Theoretical investigation on the intramolecular electron transfer between the side chains of tryptophan and tyrosine in the cyclopeptide has been performed. After geometric optimization and the double-well potential construction, reorganization energy and reaction energy difference of electron transfer are obtained. Furthermore, a corrected new two-sphere model for solvent reorganization energy, which differs from the conventional one, is deduced. For the double-well potential construction, the linear reaction coordinate approximation has been adopted. The electron transfer rate constant for the model system after deprotonation is estimated, kETÂ =Â 9.1Â ÃÂ 108 sâ1 and it is in agreement with the experimental observations. Also, the dependence of the rate constant on pH is simply discussed.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Jin Tang, Xiang-Yuan Li, Ke-Xiang Fu, Ji-Feng Liu, Shen-Zhuang Lu,