We report the first investigation of the fast excited-state intramolecular proton transfer of 3-hydroxyflavone. Picosecond stimulated emission and transient absorption spectroscopy demonstrate that the tautomer formation can be monitored by 620-nm transient absorption. The excited-state proton transfer was studied at 620 nm with femtosecond time resolution, and determined to be 240 +/- 50 fs in a nonpolar solvent environment. The fast excited-state proton transfer in methanol solution, however, was faster than the 125-fs instrument response. A simple model describing the mechanism of the fast excited-state proton transfer of 3-hydroxyflavone in different solvents is presented.
机构:
UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USAUNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USA
BENAMOTZ, D
;
HARRIS, CB
论文数: 0引用数: 0
h-index: 0
机构:
UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USAUNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USA
机构:
UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USAUNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USA
BENAMOTZ, D
;
HARRIS, CB
论文数: 0引用数: 0
h-index: 0
机构:
UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USAUNIV CALIF BERKELEY LAWRENCE BERKELEY LAB, DIV MAT & MOLEC RES, BERKELEY, CA 94720 USA