Electron Spin Resonance Spectra of Sulfinamidyl Radicals and a Comparison of Hyperfine Splitting Constants with Sulfenamidyl and Sulfonamidyl Radicals
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/63/4/63_4_1154/_pdf
Reference18 articles.
1. Reaction of a Thioaminyl Diradical with 7,7,8,8-Tetracyanoquinodimethane (TCNQ). The Formation of a Cyclophane Compound
2. ESR studies of nitrogen-centered free radicals. 33. Thioaminyl diradicals. An electron spin resonance spectroscopic study
3. ESR studies of nitrogen-centered free radicals. 32. Isolation and characterization of sulfonamidyl radical dimers
4. Electron spin resonance study of N-alkyl-N-(alkylthio)aminyl radicals
5. ESR study of persistent thioaminyls, N-(arylthio)-3,5-di-tert-butylphenylaminyls
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1. A general alkene aminoarylation enabled by N-centred radical reactivity of sulfinamides;Nature Chemistry;2024-01-16
2. Di-t-butyl Peroxyoxalate;Encyclopedia of Reagents for Organic Synthesis;2007-09-17
3. Di-t-butyl Peroxyoxalate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
4. ChemInform Abstract: ESR Studies of Nitrogen-Centered Free Radicals. Part 36. ESR Spectra of Sulfinamidyl Radicals and a Comparison of Hyperfine Splitting Constants with Sulfenamidyl and Sulfonamidyl Radicals;ChemInform;1990-09-04
5. 9.6 Thioaminyl radicals: –N•–S–, –N•–S(=O)–, –N•–SO2–;Nitrogen and Oxygen Centered Radicals
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