## Abstract Proton‐hyperfine data are reported for the radical anions generated from azulene (1) and its alkyl derivatives 2–11 in 1,2‐dimethoxyethane both ‘chemically’ with K and electrolytically. The alkyl derivatives are 1,3‐dimethyl‐ (2), 5,7‐dimethyl‐ (3), 1,3,5,7‐tetramethyl‐ (4), 2‐methyl‐ (
An ESR. and ENDOR. Study of the Radical Anions of Cyano- and Nitro-Monosubstituted Naphthalenes
✍ Scribed by Peter Fürderer; Fabian Gerson
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- German
- Weight
- 410 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^1^H‐ and ^14^N‐coupling constants have been determined by ESR. and ENDOR. spectroscopy for the radical anions of 1‐ and 2‐cyano‐, and 1‐ and 2‐nitronaphthalene.
📜 SIMILAR VOLUMES
## Abstract Radical anions often monocyclic and bicyclic azoalkanes containing the azo group in (__Z__)‐conformation, have been fully characterized by their hyperfine data with the use of ESR, ENDOR, and general‐TRIPLE‐resonance spectroscopy. These azoalkanes are represented by 3,3,5,5‐tetramethyl‐
## Abstract Radical anions of ten monocyclic and bicyclic azoalkanes containing the azo group in (Z)‐conformation, have been fully characterized by their hyperfine data with the use of ESR, ENDOR, and general‐TRIPLE‐resonance spectroscopy. These azoalkanes are represented by 3,3,5,5‐tetramethyl‐1‐p
I4N-and 'H-Coupling constants, determined by ESR, ENDOR, and general-TRIPLE-resonance spectroscopy, are reported for the radical cations of tetrazinodi(heteroarenes) 1-8. The results comply with the expectation that donor properties of these compounds are mainly due to the electron-rich dihydrotetra