The magnetic field effects on electrolysis. III. The anodic oxidation of phenylacetate ion.
スポンサーリンク
概要
- 論文の詳細を見る
In anodic oxidation of the phenylacetate ion, the formation yield of benzaldehyde increases by about 40% in the presence of a magnetic field (0.67 T), while 1,2-diphenylethane is insensitive to the field. The results are interpreted in terms of the magnetohydrodynamic mechanism.
- 公益社団法人 日本化学会の論文
著者
-
TANIMOTO Yoshifumi
Institute for Molecular Science
-
NAKAGAKI Ryoichi
Institute for Molecular Science
-
NAGAKURA Saburo
Institute for Molecular Science
-
WATANABE Takeshi
Institute for Molecular Science
-
Hiramatsu Mitsuo
Institute for Molecular Science
関連論文
- Effects of a High Magnetic Field on the Growth of 3-Dimensional Silver Dendrites
- High Magnetic Field Effect on the Growth of 3-Dimensional Silver Dendrites
- Intermediates for Photoisomerization of a Butenylnaphthalene in the Presence of Electron Acceptors as Studied by Solvenet Dependence of Magnetic Field Effects
- Investigation of the fluorescence depletion process in condensed phase
- EFFECT OF 8T STRONG STATIC MAGNETIC FIELD ON BEHAVIOR OF SOME PARAMECIA(Behavior Biology and Ecology)(Proceedings of the Seventy-Third Annual Meeting of the Zoological Society of Japan)
- Behavior of Biradicals Generated from a Norrish Type-I Reaction of 2,2-Diphenylcycloalkanones. Chain-Length Dependence and Magnetic Field Effects
- Magnetic field effects on the intramolecular photoreaction of n-alkyl anthraquinone-2-carboxylates.
- Transient absorption in the sensitized photoisomerization of stibene.
- The primary process of the photochemical formation of 1-nitrenopyrene.
- The magnetic field effects on electrolysis. II. The anodic surface oxidation of gold.
- The magnetic field effects on the electrolysis of hexacyanoferrate(II) oxidation and hexacyanoferrate(III) reduction.
- The magnetic field effects on electrolysis. III. The anodic oxidation of phenylacetate ion.
- Picosecond spectroscopy studies of the intersystem crossing of aromatic carbonyl and nitro compounds in solution.
- Charge-transfer Interaction and Chemical Reaction. V. Reaction of o-Phenylenediamine with Chloranil
- A rationalization of orientation in nucleophilic aromatic photosubstitution.