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Strained [n]cyclophanes
- Publisher
- Springer Journals
- Copyright
- Copyright © 2001 by VSP 2001
- Subject
- Chemistry; Inorganic Chemistry; Physical Chemistry
- ISSN
- 0922-6168
- eISSN
- 1568-5675
- DOI
- 10.1163/156856701753536642
- Publisher site
- See Article on Publisher Site
Abstract
Different levels of theoretical methods have been used to study a novel stable cylcophane 1,8-[1,8-naphthalenediylbis(4′,4-biphenyldiyl)]naphthalene. It was concluded that HF/3-21g* was the most efficient method for the system, which could well reproduce the experimental structure. In addition, HF/3-21g* / /B3LYP/3-21g* calculations explained the experimental observation that the cyclophane was much easier to be oxidized to the corresponding radical cation than its related compound 1,8-bisphenyl-naphthalene. It was proposed that the more effective π -π and π -cation interactions in the radical cation of the cyclophane caused the above behavior.
Journal
Research on Chemical Intermediates – Springer Journals
Published: Oct 7, 2004