1,2-Di(6-azulenyl)tetraphenylbenzenes and (6-azulenyl)pentaphenylbenzenes were synthesized by Diels-Alder reaction of di(6-azulenyl)acetylenes and 6-(phenylethynyl)azulenes with tetraphenylcyclopentadienone. Mono(6-azulenyl)benzenes exhibited a reduction wave upon cyclic voltammetry (CV). In contras
✦ LIBER ✦
Synthesis, Stabilities, and Redox Behavior of Di(1-azulenyl)(6-azulenyl)methylium Hexafluorophosphates. Generation of a Donor−Acceptor-Substituted Neutral Radical by Azulenes
✍ Scribed by Ito, Shunji; Kubo, Takahiro; Morita, Noboru; Ikoma, Tadaaki; Tero-Kubota, Shozo; Tajiri, Akio
- Book ID
- 127347904
- Publisher
- American Chemical Society
- Year
- 2003
- Tongue
- English
- Weight
- 220 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0022-3263
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
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