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EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER IN DICOUMAROL, A $CH_2$-BRIDGED DIMER OF 4-HYDROXYCOUMARIN
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  • EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER IN DICOUMAROL, A $CH_2$-BRIDGED DIMER OF 4-HYDROXYCOUMARIN
  • EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER IN DICOUMAROL, A $CH_2$-BRIDGED DIMER OF 4-HYDROXYCOUMARIN
저자명
Cho. Dae-Won
간행물명
Journal of photoscience: an international journal officail organ of the Korean Society of Photoscience
권/호정보
1995년|2권 1호|pp.13-18 (6 pages)
발행정보
한국광과학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The steady-state emission spectra of dicoumarol (DC) in ethanol and EPA have been examined at various temperatures (77-298 K). At room temperature, a fluorescence spectrum of DC in ethanol shows a emission maximum at 350 nm. In EPA a Stokes-shifted emission band appears around 470 nm in addition to the 350 nm emission, and its intensity is enhanced as temperature decreases. This emission is attributed to a zwitterionic tautomer of DC formed by a single excited-state intramolecular proton transfer (ESIPT) along the internal hydrogen-bonding. The fluorescence lifetimes have been measured at 350 and 450 nm as a function of temperature. The fluorescence decay at 350 nm is single exponential at any temperature, whereas the one at 450 nm becomes biexponential at temperatures below 250 K. These results are discussed in terms of a conformational change followed by the ESIPT. The activation energy barrier for the conformational change has been determined to be 3.7 $pm$ 0.2 kJ/mole.