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    阿布都克尤木·阿布都热西提, 阿卜杜合拜尔·米尔扎, 利小东,, 古丽加娜提·排他尔, 吐尼沙古丽·阿吾提, 司马义·努尔拉. 新型噻吩衍生物与三嗪聚合物的合成及其性能[J]. 功能高分子学报, 2014, 27(3).
    引用本文: 阿布都克尤木·阿布都热西提, 阿卜杜合拜尔·米尔扎, 利小东,, 古丽加娜提·排他尔, 吐尼沙古丽·阿吾提, 司马义·努尔拉. 新型噻吩衍生物与三嗪聚合物的合成及其性能[J]. 功能高分子学报, 2014, 27(3).
    Abdukaiyum ABDURASHID, Abduheber MIRZEHMET, LI Xiao dong, Guljannat PATTAR, Tunsagul AWUT, Ismayil NURULLA. Synthesis and Properties of Polymers Containing Thiophene Derivative and Triazine Unit[J]. Journal of Functional Polymers, 2014, 27(3).
    Citation: Abdukaiyum ABDURASHID, Abduheber MIRZEHMET, LI Xiao dong, Guljannat PATTAR, Tunsagul AWUT, Ismayil NURULLA. Synthesis and Properties of Polymers Containing Thiophene Derivative and Triazine Unit[J]. Journal of Functional Polymers, 2014, 27(3).

    Synthesis and Properties of Polymers Containing Thiophene Derivative and Triazine Unit

    • 摘要: 以四三苯基膦钯(Pd(PPh3)4)作为催化剂,通过Stille 偶联反应,2-二异丙基氨基-4,6-二氯均三嗪分别与2,5-二(三丁基锡)噻吩和2,5-二(三丁基锡)-3,4-乙撑二氧噻吩共聚合成了含2-二异丙基氨基均三嗪的两种新型π-共轭聚合物聚(2-异丙基氨基三嗪噻吩)(P1)和聚(2-异丙基氨基三嗪3,4-乙撑二氧噻吩)(P2)。采用傅里叶变换红外光谱(FT-IR)、核磁共振氢谱(1H-NMR)、紫外 可见光谱(UV-Vis)、荧光光谱(PL)、循环伏安(CV)、X射线粉末衍射(XRD)和凝胶渗透色谱(GPC)等测试手段对共聚物P1、P2进行了表征。结果表明: 所得聚合物P1、P2都有一定的结晶性,在氯仿、四氢呋喃、三氟乙酸等常用有机溶剂里有一定的溶解性。P1、P2的紫外-可见最大吸收波长分别出现在354 nm和374 nm处。 在CHCl3溶液中,P1与P2的最大发射峰分别出现在454 nm和442 nm处; P1和P1薄膜的最大发射峰分别为513 nm和493 nm。与P2相比,P1在 0~-1.8 V出现明显的n-掺杂峰。

       

      Abstract: 2-Diisopropylamino 4,6-dichlorostriazine was copolymerized with 2,5-bis(tributylstannyl)thiophene and 5,7-bis(tributylstannyl) 2,3- dihydrothieno[3,4 b][1,4]dioxin by Stille coupling using tetrakis(triphenylphosphine)palladium (Pd(PPh3)4) as catalyst to form a new type π conjugated polymers (P1 and P2) containing 2 diisopropylaminostriazine. The structures of the polymers were performed by Fourier Translation Infrared Spectroscopy (FT-IR), 1H Nuclear Magnetic Resonance (1H-NMR), Ultraviolet and Visible spectrophotometry (UV-Vis), Fluorescence Spectroscopy (PL), Gel Permeation Chromatography (GPC), Cyclic Voltammogram (CV) and X-ray Diffraction analysis (XRD). Results show that the derived polymers have certain crystallinity and solubility in common organic solvents such as tetrahydrofuran, CHCl3, CF3COOH. The UV-Vis maximum absorption peaks of polymers appear at 354 nm and 374 nm in CHCl3 .The maximum emission peaks of polymers appear at 454 nm and 442 nm in CHCl3 solution and 513 nm and 493 nm in film state. In comparison with P2, P1 has obvious n doped peaks in the regions from 0 to -1.8 V.

       

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