## Abstract Strategies for the preparation of new fluorescent oligopeptide conjugates labeled with 4‐ethoxymethylene‐2‐[1]‐naphthyl‐5(4__H__)‐oxazolone (naOx‐OEt) at the N‐terminal on solid support or in solution have been devised. These procedures are simple and easy to carry out by reacting naOx‐
Synthesis and characterization of the soluble fluorescent poly[2-decyloxy-5-(2′-(6′-dodecyloxy)naphthyl)-1,4-phenylenevinylene]
✍ Scribed by Hung-Te Chang; Hsun-Tsing Lee; Mou-Yung Yeh
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 291 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Abstract
A new soluble fluorescent polymer, poly[2‐decyloxy‐5‐(2′‐(6′‐dodecyl‐oxy)naphthyl)‐1,4‐phenylenevinylene] (DDN‐PPV), with no tolane‐bisbenzyl (TBB) structure defects is prepared by the dehydrohalogenation of 1,4‐bis(bromomethyl)‐2‐decyloxy‐5‐(2′‐(6′‐dodecyloxy)naphthyl)benzene (as monomer) in this study. The aforementioned monomer is synthesized via such chemical reactions as alkylation, bromination, and Suzuki coupling reactions. The structure and properties of the DDN‐PPV are examined by ^1^H NMR, FTIR, UV/vis, TGA, photoluminescence (PL), and electroluminescence (EL) analyses. The two asymmetric decyloxy and 6′‐dodecyloxynaphthyl substituents on the phenylene ring make the DDN‐PPV soluble in organic solvents and eliminate the TBB structure defects. With the DDN‐PPV acting as a light‐emitting polymer, a device is fabricated with a sequential lamination of ITO/PEDOT/DDN‐PPV/Ca/Ag. The EL spectrum of the device shows a maximum emission at 538 nm. The turn on voltage of the device is about 16.6 V. Its maximum brightness is 14 cd/m^2^ at a voltage of 18.2 V. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2734–2741, 2007
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