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Kenji Sakota

Researcher at Osaka City University

Publications -  51
Citations -  1235

Kenji Sakota is an academic researcher from Osaka City University. The author has contributed to research in topics: Excited state & Hydrogen bond. The author has an hindex of 21, co-authored 51 publications receiving 1153 citations. Previous affiliations of Kenji Sakota include Kyushu University.

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Excited-state double-proton transfer in a model DNA base pair : Resolution for stepwise and concerted mechanism controversy in the 7-azaindole dimer revealed by frequency- and time-resolved spectroscopy

TL;DR: In this article, the authors reviewed the results and discussions associated with stepwise and concerted mechanism controversy on ESDPT of 7AI 2 together with the excited-state dynamics associated with ESDPTs.
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Excited-state double-proton transfer in the 7-azaindole dimer in the gas phase. 3. Reaction mechanism studied by picosecond time-resolved REMPI spectroscopy.

TL;DR: The observed decay profiles of 7AI2 by exciting the origin and the intermolecular stretch fundamental in the S1 state are well reproduced by single-exponential functions with time constants of 1.9 +/- 0.9 ps and 860 +/- 300 fs, respectively, which provides clear evidence of the concerted mechanism of ESDPT in 7 AI2.
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Excited-state intramolecular proton transfer in photochromic jet-cooled N-salicylideneaniline

TL;DR: In this article, the laser induced fluorescence and dispersed fluorescence spectra of jet-cooled N-salicylideneaniline were observed in a supersonic free jet for the first time.
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Excited-state double-proton transfer in the 7-azaindole dimer in the gas phase. 2. Cooperative nature of double-proton transfer revealed by H/D kinetic isotopic effects.

TL;DR: The observed H/D kinetic isotope effects imply that the ESDPT reaction of 7AI2 has a "cooperative" nature; i.e., the motion of the two moving protons strongly couples each other through the electron motions.
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Cooperative triple-proton/hydrogen atom relay in 7-azaindole(CH3OH)2 in the gas phase: remarkable change in the reaction mechanism from vibrational-mode specific to statistical fashion with increasing internal energy.

TL;DR: The results suggest that the ESTPT/HT reaction in 7AI(CH(3)OH)2-d(0) directly proceeds from the photoexcited states with the internal energy less than approximately 600 cm(-1), but it occurs from the isoenergetically vibrational-energy redistributed states when theinternal energy is large.