中國醫藥大學機構典藏 China Medical University Repository, Taiwan:Item 310903500/7486
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 29490/55136 (53%)
Visitors : 1504933      Online Users : 254
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.cmu.edu.tw/ir/handle/310903500/7486


    Title: Synthesis, Optical Properties, and Characterization of New Soluble Conjugated Poly(p-phenylenevinylene) Derivatives Constituted of Alternating Pyrazole and 1,3,4-Oxadiazole Moieties
    Authors: (En-Ming Chang);(Cheng-Tien, Lee);(Chun-Yen Chen);翁豐富(Wong, Fung Fuh)*;(Mou-Yung, Yeh)*
    Contributors: 藥學院藥物化學研究所
    Date: 2008-05
    Issue Date: 2009-08-26 16:26:38 (UTC+8)
    Abstract: Two new soluble poly(p-phenylenevinylene) derivatives with 1,3,4-oxadiazole and pyrazole rings along the main core were successfully synthesized by 1,3-dipolar addition, dehydration, and Heck coupling reaction. The new conjugated polymers are soluble in common organic solvents afforded by the fully conjugated backbone with soluble dedecyloxy side groups. The polymers showed relatively high glass-transition temperatures (~150°C) and good satisfactory thermal stability. Solutions of the polymers emitted bluish-green light with photoluminescence (PL) emission maxima around 530–540 nm. The PL spectrum for polymers of thin films, with a maximum at 570 nm, shows a red-shift (~35 nm) with respect to the solution spectrum. Cyclic voltammetry displayed that both conjugated polymers had reversible reduction and irreversible oxidation, making them n-type electroluminescent materials. The electron affinity of new polymers was estimated as 2.76–2.81 eV. The weight-average molecular weights (Mw) of the new soluble polymers were in the range 3400–3500.
    Relation: AUSTRALIAN JOURNAL OF CHEMISTRY 61(5)342~349
    Appears in Collections:[Graduate Institute of Pharmaceutical Chemistry] Journal articles

    Files in This Item:

    File SizeFormat
    58KbUnknown278View/Open


    All items in CMUR are protected by copyright, with all rights reserved.

     


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback