AKIO ICHIMURA

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Organization: Osaka City University , Japan
Department:
Title: Professor(PhD)
Co-reporter:Sachiko Tanimoto and Akio Ichimura
Journal of Chemical Education 2013 Volume 90(Issue 6) pp:778-781
Publication Date(Web):April 26, 2013
DOI:10.1021/ed200604m
A laboratory experiment for undergraduate students who are studying homogeneous and heterogeneous electron-transfer reactions is described. Heterogeneous or electrode reaction kinetics can be examined by using the electrochemical reduction of three FeIII/FeII redox couples at platinum and glassy carbon disk electrodes. Cyclic voltammetric measurement is suitable for determining the electrode-reaction rate constants. The dependence of the rate constant on the electrode materials enables the students to discriminate and discuss the mechanism of the electrode reaction. The experiment is completed in a 5-h laboratory period for pairs of students in analytical chemistry lab class. This material is also suitable for an inorganic chemistry lab class.Keywords: Analytical Chemistry; Aqueous Solution Chemistry; Coordination Compounds; Cyclic Voltammetry; Electrochemistry; Inorganic Chemistry; Instrumental Methods; Kinetics; Laboratory Instruction; Oxidation/Reduction; Upper-Division Undergraduate;
Co-reporter:Ryoko Santo;Riichi Miyamoto;Rika Tanaka Dr.;Takanori Nishioka Dr.;Kazunobu Sato Dr.;Kazuo Toyota Dr.;Makoto Obata Dr.;Shigenobu Yano Dr.;Isamu Kinoshita Dr. Dr.;Takeji Takui Dr.
Angewandte Chemie 2006 Volume 118(Issue 45) pp:
Publication Date(Web):20 OCT 2006
DOI:10.1002/ange.200603127

Alles ändert sich: Der im Bild gezeigte stabile, diamagnetische, trigonal-bipyramidale CuIII-Komplex, der bei der Einelektronenoxidation eines CuII-Komplexes erhalten wird, lagert sich bei der Zugabe von Cl-Ionen in einen paramagnetischen, oktaedrischen CuIII-Komplex um. Die Charakterisierung der Komplexe und Dichtefunktionalrechnungen sprechen dafür, dass die urspüngliche Einelektronenoxidation metall- und nicht ligandenzentriert ist.

Co-reporter:Ryoko Santo;Riichi Miyamoto;Rika Tanaka Dr.;Takanori Nishioka Dr.;Kazunobu Sato Dr.;Kazuo Toyota Dr.;Makoto Obata Dr.;Shigenobu Yano Dr.;Isamu Kinoshita Dr. Dr.;Takeji Takui Dr.
Angewandte Chemie International Edition 2006 Volume 45(Issue 45) pp:
Publication Date(Web):20 OCT 2006
DOI:10.1002/anie.200603127

All change: The stable, diamagnetic, trigonal-bipyramidal CuIII complex (see picture) arising from one-electron oxidation of a CuII complex undergoes conversion into a paramagnetic octahedral CuIII complex upon addition of Cl ions. Characterization of the complexes and density functional calculations indicate that the initial one-electron oxidation is metal- rather than ligand-centered.

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