ESR13C Hyperfine Structures of the Meta-substitutedt-Butyl Biphenyl Anion Radical
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/43/12/43_12_3956/_pdf
Reference5 articles.
1. 1,3,5-Tri-t-butylbenzene and Some Derivatives1
2. Factors Determining the Course and Mechanisms of Grignard Reactions. IV. The Effect of Metallic Halides on the Reaction of Aryl Grignard Reagents and Organic Halides1
3. Theoretical Interpretation of Carbon‐13 Hyperfine Interactions in Electron Spin Resonance Spectra
4. Electron spin resonance spectra of some isotopically substituted hydrocarbon radicals
5. ESR Studies of the Negative Ions of Biphenyl Derivatives. III. Restricted Rotation of Alkyl Group in SomeorthoorparaHigher Alkylated Biphenyl Anion Radicals
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2. Polymenthylenebiphenyl polyanions by metallation—elimination;Tetrahedron Letters;1982-01
3. tert-Butylierung von Biphenyl; Strukturermittlung der Reaktionsprodukte durch unabhängige Synthesen;Liebigs Annalen der Chemie;1980-12-23
4. ENDOR Studies of Alkylated Biphenyl Anion Radicals in Solution. Relation between Molecular Size and Optimum Temperature of ENDOR Enhancement;Bulletin of the Chemical Society of Japan;1977-01
5. ESR Studies of the Cation Radicals Produced by SbCl5Oxidation of Some Biphenyls withortho- andpara-Dialkyl Substituents;Bulletin of the Chemical Society of Japan;1973-10
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