Various radical cations, in which two terminal 1,4dimethoxybenzene units are anellated to [2.2]paracyclophane (2b and anthracene bridges (5 โข+ ), have been studied by ESR and ENDOR spectroscopy. In the syn-and anti-naphthalenophane radical cations 2b โข+ and 3b โข+ the delocalization of the unpaired
โฆ LIBER โฆ
A competition reaction between substitution and electron transfer of 1, 4-dimethoxybenzenes in conc. H2sO4
โ Scribed by Akira Nishinaga; Peter Ziemek; Teruo Matsuura
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 117 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
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1998 structure structure (organic substances) K 9000 35 -033 Intramolecular Electron Transfer Between Terminal 1,4-Dimethoxybenzene Units in Radical Cations with a [2.2](1,4)Naphthalenophane, [2.2](1,4)Anthracenophane, and Pentacene Skeleton. -Whereas the syn-and anti-conformer of radical cation (I)
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