Synthesis and redox behavior of 1,3,5- and 1,2,4-tri(6-azulenyl)benzene derivatives
✍ Scribed by Shunji Ito; Haruki Inabe; Tetsuo Okujima; Noboru Morita; Masataka Watanabe; Nobuyuki Harada; Kimiaki Imafuku
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 111 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Described herein is a cobalt-mediated cyclooligomerization of mono-and di(6-azulenyl)acetylenes to afford 1,3,5-and 1,2,4-tri(6-azulenyl)benzene derivatives and (h 5 -cyclopentadienyl)[tetra-and di(6-azulenyl)cyclobutadiene]cobalt complexes. The redox behavior of these novel tri(6-azulenyl)benzene derivatives and [tetra-and di(6-azulenyl)cyclobutadiene]cobalt complexes examined by cyclic voltammetry is also described.
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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
## 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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