| Literature DB >> 18656945 |
Grigory V Zyryanov1, Manuel A Palacios, Pavel Anzenbacher.
Abstract
1,4-Diarylpentiptycenes (1a-e) were synthesized from 1,4-dichloro- or 1,4-difluoro-2,5-diarylbenzene derivatives by double base-promoted dehydrohalogenation to give corresponding arynes, which in the presence of anthracene undergo cycloaddition providing 1,4-diarylpentiptycenes in moderate overall yields. The resulting 1,4-diarylpentiptycenes show fluorescence modulated by the 1,4-aryl residues. The fluorescence is quenched in the presence of vapors of nitroaromatic compounds suggesting potential application in sensing of explosives.Entities:
Year: 2008 PMID: 18656945 DOI: 10.1021/ol801030u
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005