Effect of the Chemical Modification by Viologen on the Reduction of Metmyogloblin
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概要
- 論文の詳細を見る
- 1992-07-05
著者
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Tsukahara Keiichi
Department Of Chemistry Faculty Of Science Nara Women's University
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TODOROBARU Hiromi
Department of Chemistry, Faculty of Science, Nara Women's University
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Todorobaru Hiromi
Department Of Chemistry Faculty Of Science Nara Women's University
関連論文
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- Electrochemical and Phosphorescent Properties of New Ir(III) Complexes Coordinated by Various Bipyridine Derivatives
- Kinetics and Mechanisms of the Reaction of PH_2O_2^- with O_2, Photocatalyzed by [Ru(bpy)_3]^ (bpy=2,2'-bipyridine), Forming Peroxodiphosphate Ions in an Aqueous Solution
- A Novel Reaction of HCrO_4^- with PH_2O_2^-, Induced by Molecular Oxygen, Forming Peroxodiphosphate Ions in an Aqueous Solution
- Stereoselective Photoinduced Electron Transfer of Zinc Myoglobin with Optically Active Viologens
- Intracomplex Quenching by Copper(II)Ion of Excited Singlet and Triplet States of Zinc Myoglobin Modified with Diethylenetriaminepentaacetic Acid
- Syntheses, Characterizations, and Redox Behavior of Optically Active Viologens and Bisviologens
- Stereoselective Luminescence Quenching in the Complex of Excited Triplet State of Δ-Tris(2, 2'-bipyridine)ruthenium(II)with Optically Active Viologens in an Aqueous Solution^1
- Direct Comparison of Chiral Substituent Effects for Viologens in Stereoselective Photoinduced Electron-Transfer Reactions with Zinc Myoglobin
- Formation of Peroxodiphosphate by the Copper(II)-Catalyzed Oxidation Reaction of the Phosphinate Ion by the Molecular Oxygen. Kinetics and Mechanisms in Aqueous Solutions
- Chiral Recognition in Disproportionation of Monoradical Cation of Optically Active Bisviologen in an Aqueous Solution
- Stereoselective Photoinduced Electron-Transfer Reaction between Zinc Myoglobin and New Chiral Quinolinium Ions
- Mechanisms of Oxidation Reactions of Iodide and Hexacyanoferrate(II) Ions, Induced BY the Reaction betwiin Phosphinate Ion and Molecular Oxygen in an Aqueous Solution
- Assembly of Diethylenetriaminepentaacetatocobaltate(III) Complexes on the Surface Lysine Residues of Myoglobin
- Intramolecular Electron-Transfer Pathway for Deoxy and Zinc Myoglobins Modified with N, N, N', N'', N''-Diethylenetriaminepentaacetatocobaltate(III)
- Kinetics and Mechanism of the Oxidation of [Fe(CN)_6]^ to [Fe(CN)_6]^, Induced by the Reaction between Cu^ and I^- in Aqueous Solution. Oxidation Reaction by a Radical Anion I_2^
- Kinetics and Mechanism of the Copper(II)-Catalyzed Oxidation of the Iodide Ion by Chromate(VI) Ion in an Aqueous Solution
- Stereoselective Electron-Transfer Reactions of Myoglobin and Cytochrome C with Chiral Viologen-Radical Cations
- Kinetics and Mechanism of the Copper(II)-Catalyzed Oxidation of the Iodide Ion to Iodine by the Vanadium(V) Ion in an Aqueous Solution
- Electron-Transfer Quenching and Thermal Backward Electron-Transfer Reactions of Zinc Myoglobin Controlled by Conformational Change
- Effect of the Chemical Modification by Viologen on the Reduction of Metmyogloblin
- Intramolecular Electron Transfer of Cytochrome c Modified with N, N, N', N'', N''-Diethylenetriaminepentaacetatocobaltate(III)
- Stereoselective Electron-Transfer Reaction between Metmyoglobin and Chiral Viologen-Radical Cation through Pre-Complexation
- Kinetics and Mechanisms of Photoinduced Reduction of Methylviologen by N-Alkyltetraphenylporphyrinatozinc(II) in Methanol
- Kinetics and Mechanisms of the Vanadium(IV)-Catalyzed Oxidation of Iodide Ion in the Presence of Molecular Oxygen in an Acid Solution
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- Kinetics and mechanisms of the photo-induced oxidation of ascorbic acid by molecular oxygen catalyzed by ruthenium(II) complexes containing 2,2'-bipyridine and 2,2'-bipyrazine.
- Intra- and intermolecular electron-transfer reaction of viologen-linked copper(II) Schiff base complexes.
- Kinetics and Mechanism of Reduction of Metmyoglobins by Dithionite. Role of the Heme Propionates.
- The reduction of cobalt(III) complexes by ascorbic acid. II. The kinetics and mechanisms of the reactions of diaqua and aquahydroxo macrocyclic N4 complexes.
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