| Literature DB >> 17607793 |
Junya Chiba1, Sakiko Takeshima, Kikyo Mishima, Hajime Maeda, Yasuaki Nanai, Kazuhiko Mizuno, Masahiko Inouye.
Abstract
DNA-like fluorescent oligomers composed of alkynyl beta-D-ribofuranosides bearing pyrene, perylene, and anthracene as a fluorophore were synthesized by solid-phase DNA synthesis. The fluorescent oligomers possess the defined number and order of the fluorophores. In these oligomers, the adjacent fluorophores efficiently interact with each other by hydrophobic interactions in their electronic ground states in a face-to-face fashion. The predominant excimer emissions were observed from not only the homooligomers (pyrene-pyrene and perylene-perylene systems) but also the heterooligomers (pyrene-perylene, pyrene-anthracene, and perylene-anthracene systems) in aqueous media.Entities:
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Year: 2007 PMID: 17607793 DOI: 10.1002/chem.200700559
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236