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Published on: March 9, 2012
Excited-state proton transfer reactions of 10-hydroxycamptothecin
Kyril M Solntsev1, Erica N Sullivan, Laren M Tolbert
1School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta 30332-0400, USA. solntsev@chemistry.gatech.edu
Abstract:
Time-resolved and steady-state emission characterization of 10-hydroxycamptothecin reveals a rich but less complex proton-transfer behavior than its parent hydroxyquinoline. The electronic effect of the additional electron-withdrawing ring makes the excited-state both less basic and more acidic than the parent and adds to the class of high-acidity excited-state proton donors in photochemistry and photobiology.
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