首页> 外文OA文献 >Probing interchain interactions in emissive blends of poly [2-metboxy-5-(2 '-ethylhexyloxy)-p-phenylenevinylene] with polystyrene and poly(styrene-co-2-ethylhexyl acrylate) by fluorescence spectroscopy
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Probing interchain interactions in emissive blends of poly [2-metboxy-5-(2 '-ethylhexyloxy)-p-phenylenevinylene] with polystyrene and poly(styrene-co-2-ethylhexyl acrylate) by fluorescence spectroscopy

机译:荧光光谱法研究聚[2-甲基-5-(2'-乙基己氧基)-对亚苯基亚乙烯基]与聚苯乙烯和聚(苯乙烯-丙烯酸-2-乙基己酯)的发射混合物中的链间相互作用

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摘要

We present dynamic and static photoluminescence studies on polymer blends of conjugated poly [2-methoxy-5-(2'-ethylhexyloxy)-p-phenylenevinylene] (MEH-PPV) with polystyrene-co-1-pyrenyl methyl methacrylate and its copolymer poly(styrene-co-2-ethylhexyl acrylate-co-1-pyrenylmethyl methacrylate) (with 9 mol% and 19 mol% of 2-ethylhexyl acrylate units and 0.06 mol% of 1-pyrenyl). Pyrenyl-labeled polystyrene and its copolymers were synthesized by emulsion polymerization and characterized by C-13 and H-1-NMR, FTIR, GPC, DSC, and UVVis. Spin-coating films of the blends were prepared from chloroform solutions with 0.1, 0.5, 1.0, and 5.0 wt% of MEH-PPV The miscibility of these systems was studied by non-radiative energy transfer processes between the 1-pyrenyl moieties (the energy donor) and MEH-PPV (the energy acceptor). The relative emission intensities and the fluorescence lifetimes of the donor showed that the miscibility of MEH-PPV and the copolymers is greater than that of MEH-PPV and polystyrene and this was confirmed by epifluorescence optical microscopy and scanning electron microscopy.
机译:我们目前对共轭聚[2-甲氧基-5-(2'-乙基己基氧基)-对亚苯基亚乙烯基](MEH-PPV)与聚苯乙烯-co-1-甲基丙烯酸甲基苯酯及其共聚物的共混物的动态和静态光致发光研究(苯乙烯-丙烯酸2-乙基己基酯-甲基丙烯酸1-吡啶基甲基酯)(具有9mol%和19mol%的丙烯酸2-乙基己酯单元和0.06mol%的1-吡啶基)。 emulsion烯标记的聚苯乙烯及其共聚物是通过乳液聚合合成的,并通过C-13和H-1-NMR,FTIR,GPC,DSC和UVVis进行表征。共混物的旋涂膜是由含0.1、0.5、1.0和5.0 wt%MEH-PPV的氯仿溶液制备的。这些体系的混溶性是通过1-吡啶基部分之间的非辐射能量转移过程(能量供体)和MEH-PPV(能量受体)。供体的相对发射强度和荧光寿命表明,MEH-PPV与共聚物的混溶性大于MEH-PPV与聚苯乙烯的混溶性,这通过表面荧光光学显微镜和扫描电子显微镜得到了证实。

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    De Andrade, ML; Atvars, TDZ;

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  • 年度 2015
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  • 原文格式 PDF
  • 正文语种 eng
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