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Shiro Hikichi

Researcher at Kanagawa University

Publications -  113
Citations -  3803

Shiro Hikichi is an academic researcher from Kanagawa University. The author has contributed to research in topics: Ligand & Catalysis. The author has an hindex of 35, co-authored 105 publications receiving 3599 citations. Previous affiliations of Shiro Hikichi include Tokyo Institute of Technology & University of Tokyo.

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Acid–base catalyses by dimeric disilicoicosatungstates and divacant γ-Keggin-type silicodecatungstate parent: Reactivity of the polyoxometalate compounds controlled by step-by-step protonation of lacunary WO sites

TL;DR: The catalytic properties of disilicoicosatungstates, [{γ-SiW10O32(H2O)2}2(μ-O)4− (2) and their parent divacant γ-Keggin type silicodecatungstate as discussed by the authors, toward C-C bond formation reactions have been investigated.
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Thermally stable coordinatively unsaturated alkyl complexes resistant to β-hydride elimination: TpiPrM–CH2CH3 (M = Co, Fe)

TL;DR: Coordinatively unsaturated hydrocarbyl complexes bearing β-hydrogen atoms, TpiPrM-CH2CH3 [M = Fe, Co; TPIPr = hydrotris(3,5-diisopropylpyrazolyl)borate], 14e and 15e species, respectively, are prepared; they are resistant to β-oxide elimination as mentioned in this paper.
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A Coordinatively Unsaturated Species with an Agostic C−H Interaction, [(κ4-TpiPr)Ru(dppe)]OSO2CF3, and Its Addition Reaction

TL;DR: In this article, the substitution reaction of the cationic aquo−ruthenium complex [TpiPrRu(dppe)(OH2)]OTf was shown to have an agostic interaction with a methyl C−H bond in the isopropyl substituent of the TpiPr ligand.
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N/O- and C-Bound (Enolato)palladium Complexes with Hydrotris(pyrazolyl)borato Ligands (TpR: R = iPr2, Me2) Obtained via Dehydrative Condensation between the Hydroxo Complexes TpRPd(Py)OH and Active Methylene Compounds: Factors Determining the Isomer Distribution and Dimerization of Cyano Compounds

TL;DR: In this paper, a hydroxopalladium complex bearing the TpiPr2 ligand was analyzed with active methylene compounds, X−CH2−Y 2 [dicyanomethane (2a), methyl cyanoacetate (2b), benzoylaceton...
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Hydrogen bonding interaction between imidazolyl N-H group and peroxide : Stabilization of Mn(III)-peroxo complex TpiPr2Mn(η2-O2)(imMeH) (imMeH = 2-methylimidazole)

TL;DR: A mononuclear side-on peroxo managanese (III) complex, TpiPr2Mn(η2-O2)(imMeH) (3) was prepared by the reaction of [TpiPr 2Mn (O)]2 with excess amount of H2O2 in the presence of 2-methylimidazole (IMMeH), its X-ray structure clearly demonstrated the involvement of intermolecular hydrogen bonding interaction between η 2-peroxide and imidazolyl N-H functional