| Literature DB >> 15195299 |
Jungho Jo1, Chunyan Chi, Sigurd Höger, Gerhard Wegner, Do Y Yoon.
Abstract
An efficient synthesis of 9,9-bis(2-ethylhexyl)fluorene oligomers up to the heptamer is reported, with repetitive Suzuki and Yamamoto coupling reactions employed in the synthesis. The key steps for preparation of the essential intermediates include Pd-catalyzed transformation of aryl bromides to aryl boronic esters (Miyaura reaction) and the application of the much higher reactivity of aryl boronic esters over aryl bromides in the Pd-catalyzed cross-coupling reaction with aryl diazonium salts. Variation of the UV/Vis absorption and photoluminescence characteristics with chain length is reported. Moreover, glass transition and liquid-crystal characteristics of the oligomers are described and compared with those of the polymer.Entities:
Mesh:
Substances:
Year: 2004 PMID: 15195299 DOI: 10.1002/chem.200305659
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236