N
Nobuyuki Nishi
Researcher at National Institutes of Natural Sciences, Japan
Publications - 26
Citations - 756
Nobuyuki Nishi is an academic researcher from National Institutes of Natural Sciences, Japan. The author has contributed to research in topics: Excited state & Acetylide. The author has an hindex of 15, co-authored 26 publications receiving 718 citations. Previous affiliations of Nobuyuki Nishi include Graduate University for Advanced Studies & Tohoku University.
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Conversion of liquids to cluster beams by adiabatic expansion of liquid jets: mass spectrometric analysis of molecular association in aqueous solution systems
Nobuyuki Nishi,Kazunori Yamamoto +1 more
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Synthesis and characterization of mesoporous carbon nano-dendrites with graphitic ultra-thin walls and their application to supercapacitor electrodes
TL;DR: Mesoporous carbon nano-dendrites (MCNDs) with ultra-thin graphitic walls are synthesized by controlling the highly exothermic segregation reaction of silver acetylide into a carbon skeleton and silver vapor as discussed by the authors.
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Ultrafast excited-state dynamics in photochromic N-salicylideneaniline studied by femtosecond time-resolved REMPI spectroscopy
TL;DR: Investigation of ultrafast processes in photoexcited N-salicylideneaniline with femtosecond time-resolved resonance-enhanced multiphoton ionization spectroscopy reveals that an internal conversion to the S(1)(n,pi( *)) state of the enol form may provide opposite effect on the quantum yield of photochromic products.
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Ultrafast Intersystem Crossing of 4-Thiothymidine in Aqueous Solution
Yosuke Harada,Chie Okabe,Takashi Kobayashi,Tadashi Suzuki,Teijiro Ichimura,Nobuyuki Nishi,Yao-Zhong Xu +6 more
TL;DR: In this paper, the authors investigated the photophysical pathway of UVA-sensitive 4-thiothymidine in aqueous solution by pump-probe transient absorption and found that the triplet form is the initial toxic source to DNA and other biomolecules.
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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.