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    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/44215

    Title: New Thiophene-Linked Conjugated Poly(azomethine)s: Theoretical Electronic Structure, Synthesis, and Properties
    Authors: Tsai, Fu-chuan;Chang, Chao-ching;Liu, Cheng-liang;Chen, Wen-chang;Jenekhe, Samson A.
    Contributors: 淡江大學化學工程與材料工程學系
    Date: 2005-03-08
    Issue Date: 2010-03-09 10:03:32 (UTC+8)
    Publisher: Washington: American Chemical Society (ACS)
    Abstract: We report a joint theoretical and experimental study of several new thiophene-based poly(azomethine)s. Hybrid density functional theory (DFT) method was used to calculate the optimized geometry and electronic structure of poly(azomethine)s. Theoretical band gaps of the new thiophene-based poly(azomethine)s were in the range 2.33−2.67 eV, which are smaller than that of the phenylene-based polymer. The variation of the backbone ring (fluorene, carbazole, or naphthalene) or donor/acceptor side group on the phenylene ring significantly affected the dihedral angles and resulted in the variation of electronic properties (ionization potential, electron affinity, and band gap) of the poly(azomethine)s. Five soluble new conjugated poly(azomethine)s derived from the polymerization of 2,5-diformyl-3-hexylthiophene (DFHT) with various diamines were prepared and characterized. The optical and electrochemical band gaps of the polymer films were in the ranges 2.21−2.28 and 2.13−2.24 eV, respectively. The trend of the effect of the backbone ring or side chain on the experimental electronic properties is in good agreement with the theoretical results. Our study demonstrates how the electronic properties of conjugated poly(azomethine)s can be tuned by the backbone ring or side group, which could be important for electronic or optoelectronic applications of the materials.
    Relation: Macromolecules 38, pp.1958-1966
    DOI: 10.1021/ma048112o
    Appears in Collections:[化學工程與材料工程學系暨研究所] 期刊論文

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