D
Daisuke Yokogawa
Researcher at Nagoya University
Publications - 73
Citations - 1191
Daisuke Yokogawa is an academic researcher from Nagoya University. The author has contributed to research in topics: Solvation & Density functional theory. The author has an hindex of 17, co-authored 64 publications receiving 1029 citations. Previous affiliations of Daisuke Yokogawa include National Institute for Nanotechnology & Osaka University.
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Super-Reduced Polyoxometalates: Excellent Molecular Cluster Battery Components and Semipermeable Molecular Capacitors
TL;DR: Evidence is presented that the super-reduction is accompanied by metal-metal bond formation, beginning from the 12th to 14th excess electron transferred to the cluster, and this "semiporous molecular capacitor" structure is likely the reason for the effective electron uptake in POMs.
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New generation of the reference interaction site model self-consistent field method: introduction of spatial electron density distribution to the solvation theory.
TL;DR: The authors propose the new generation of the reference interaction site model self-consistent field (RISM-SCF) method for the solvation effect on the electronic structure of a solute molecule, in which the procedure proposed by Gill et al. is adopted.
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A Strap Strategy for Construction of an Excited‐State Intramolecular Proton Transfer (ESIPT) System with Dual Fluorescence
Naoya Suzuki,Aiko Fukazawa,Kazuhiko Nagura,Shohei Saito,Hirotaka Kitoh-Nishioka,Daisuke Yokogawa,Stephan Irle,Shigehiro Yamaguchi +7 more
TL;DR: An amine-embedded flexible alkyl strap has been incorporated into an emissive boryl-substituted dithienylpyrrole skeleton as a new entity of excited-state intramolecular proton transfer (ESIPT) chromophores that shows a dual emission.
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A Theoretical Analysis of a Diels−Alder Reaction in Ionic Liquids
TL;DR: The Diels-Alder reaction of cyclopentadinene with methyl acrylate in room-temperature ionic liquids (RTILs) is theoretically examined and the origin of the relatively moderate solvation effects of RTILs and the mechanism of endo-exo selectivity is examined.
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Near infrared two-photon-excited and -emissive dyes based on a strapped excited-state intramolecular proton-transfer (ESIPT) scaffold
Naoya Suzuki,Kayo Suda,Daisuke Yokogawa,Hirotaka Kitoh-Nishioka,Stephan Irle,Akihiro Ando,Luis M. G. Abegão,Luis M. G. Abegão,Kenji Kamada,Aiko Fukazawa,Shigehiro Yamaguchi +10 more
TL;DR: In this article, a dialkylamine-strapped 2,5-dithienylpyrrole scaffold was used as an ESIPT scaffold and electron-accepting units were added to the terminal positions of this scaffold to generate acceptor-π-donor-,π-acceptor, π-conjugated compounds with red-shifted fluorescence.