In contrast to recent claims by Rhodes and Glidewell, comparison of both ESR and electronic absorption spectra shows that the photoproduct of the recently characterized radical cation of bicyclo[ 3.3.0]octa-2,6-diene-4,8-diyl is identical to the 1,4dihydropentalene radical cation, i.e. a linear conj
The synthesis and properties of azuleno[1,2-d]bicyclo[5.4.1]dodeca-1,4,6,8,9a-pentaen-3-one and its cationic species
β Scribed by Shigeyasu Kuroda; Sunao Maeda; Syuzi Hirooka; Masahiro Ogisu; Kazuo Yamazaki; Ichiro Shimao; Masafumi Yasunami
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 252 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The titled azuleno-annulenone was synthesized and in strong acid its protonated cationic species was generated, which is the first 18-pi electron diatropic condensed bridged annulene as shown in its 'H-NMR spectrum.
Although the syntheses and properties of the condensed 18-pi electron systems such as azulenoazulenes have been reported," no condensed system such as azulene fused with bridged annulenone has so far been investigated. In this paper we wish to report the synthesis and properties of titled azuleno-bridged annulenone and its cationic species generated in strong acid.
π SIMILAR VOLUMES
Fifteen title compounds, e.g. (I)-(III), are prepared essentially as described previously. Evaluation of their absorption, emission and laser properties shows that N-allyl substituted derivatives (Ia) and (IIa) have high fluorescence quantum yields and laser efficiencies of 137 and 140%, respectivel
## 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 βFull Textβ option. The original article is trackable v