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Koichiro Jitsukawa

Researcher at Nagoya Institute of Technology

Publications -  109
Citations -  2088

Koichiro Jitsukawa is an academic researcher from Nagoya Institute of Technology. The author has contributed to research in topics: Ligand & Hydrogen bond. The author has an hindex of 25, co-authored 109 publications receiving 2029 citations.

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Synthesis, Structure, and Spectroscopic Properties of [Feiii (tnpa)(OH)(PhCOO)]ClO4 : A Model Complex for an Active Form of Soybean Lipoxygenase-1.

TL;DR: The cis configuration between the hydroxo and the carboxylato and the three amino groups of the tetradentate, tripodal ligand tris(6-neopentylamino-2-pyridylmethyl)amine favors the formation of hydrogen bonds which stabilize the hydoxo-Feiii complex 1.
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An infinite chiral single-helical structure formed in Cu(II)-l-/d-glutamic acid system

TL;DR: In this paper, the reaction of Cu(ClO4)2·6H2O with l -glutamic acid ( l -glu) in 1:1 or 1:2 molar ratio at pH 5 gave only the complex [Cu( l −glu)-(H 2O)]·H2
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Steric and hydrogen-bonding effects on the stability of copper complexes with small molecules.

TL;DR: The UV-vis and ESR spectral data indicate that the increase of NH(2) groups of ligands causes the structural change from trigonal-bipyramidal to square-pyramidal geometry, which is regulated by a combination of steric repulsion and hydrogen bond.
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Preparation, Structure Characterization, and Oxidation Activity of Ruthenium Complexes with Tripodal Ligands Bearing Noncovalent Interaction Sites

TL;DR: Ruthenium(II/III) complexes with tripodal tris(pyridylmethyl)amine ligands bearing one, two, or three pivalamide groups or neopentylamine ones at the 6-position of the pyridine ring have been synthesized and structurally characterized.
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Copper hydroperoxo species activated by hydrogen-bonding interaction with its distal oxygen.

TL;DR: A novel copper(II)[bond]OOH complex with functional ligand that can form a hydrogen bond with the distal oxygen of hydroperoxide has been designed and prepared as a structural/functional model of dopamine beta-hydroxylases, whose spectroscopic characterization and decomposition rates have indicated that the Hydroperoxide is activated through the hydrogen-bonding interaction with thedistal oxygen.