The One-Electron Reduction of Carbonium Ions. V. A Kinetic Study on the Reduction of the Substituted Cyclopropenium Ions with Cr(II)
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/46/12/46_12_3881/_pdf
Reference15 articles.
1. One-Electron Reduction of Carbonium Ions. III. The Effect of Added Anions on the Rate of Reduction of the Tropylium Ion with Cr(II)
2. One-Electron Reduction of Carbonium Ions. IV. A Kinetic Study on the Reduction of the Substituted Tropylium Ions with Cr(II)
3. The sym-Triphenylcyclopropenyl Cation, a Novel Aromatic System1
4. THE SYNTHESIS OF BIS-TRIPHENYLCYCLOPROPENYL, AN UNDISSOCIATED DIMER OF THE TRIPHENYLCYCLOPROPENYL RADICAL, AND ITS ISOMERIZATION TO HEXAPHENYLBENZENE
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2. Stable carbocations having the intramolecular charge-transfer interaction.;Journal of Synthetic Organic Chemistry, Japan;1987
3. Linear free-energy relationships between stability parameters of substituted tropylium and cyclopropenylium ions as measured by reduction rate with chromium(II), reduction potential, charge-transfer energy, and pKR+ values;Tetrahedron;1983-01
4. Syntheses and Properties of the Polymethylenebis(diphenylcyclopropenium) Dications;Bulletin of the Chemical Society of Japan;1982-08
5. Synthesis and Properties of Bis(cyclopropylphenyl)cyclopropenones and the Tris(p-cyclopropylphenyl)cyclopropenium Ion;Bulletin of the Chemical Society of Japan;1979-03
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