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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Self-assembly of hydrogen-bonded comb copolymer complexes of poly(p-hydroxystyrene) and 4-alkylpyridine amphiphiles
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Self-assembly of hydrogen-bonded comb copolymer complexes of poly(p-hydroxystyrene) and 4-alkylpyridine amphiphiles

机译:聚(对羟基苯乙烯)与4-烷基吡啶两亲物的氢键结合的梳型共聚物配合物的自组装

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摘要

The self-assembly of the hydrogen-bonded complexes between poly(p-hydroxystyrene) (PpHS) and 4-alkylpyridine amphiphiles is studied using infrared spectroscopy, differential scanning calorimetry, polarized optical microscopy, transmission electron microscopy and small-and wide-angle X-ray scattering. Interesting differences are observed with the well-studied inverted system of poly(4-vinylpyridine) and alkylphenol amphiphiles. When the alkyl tails of the 4-alkylpyridine amphiphiles are long enough, 19 and 21 respectively, an ordered lamellar structure is formed on cooling where the ordering and crystallization of the alkyl tails occur quasi simultaneously. For a shorter alkyl tail of length 17 no ordered structure is formed. This is quite different from the inverted P4VP/alkylphenol systems, where already for an alkyl tail of length 15, i.e., pentadecylphenol, an ordered structure is formed below ca. 55 degrees C, followed by crystallization of the alkyl tails at ca. 20 degrees C. This can be attributed to the possibility of (intramolecular) hydrogen bond formation of PpHS. (C) 2016 Elsevier Ltd. All rights reserved.
机译:使用红外光谱,差示扫描量热法,偏光光学显微镜,透射电子显微镜和小和广角X射线研究了聚(对羟基苯乙烯)(PpHS)和4-烷基吡啶两亲物之间的氢键配合物的自组装射线散射。在对聚(4-乙烯基吡啶)和烷基酚两亲物的深入研究的倒置系统中观察到有趣的差异。当4-烷基吡啶两亲物的烷基尾足够长时,分别为19和21,在冷却时形成有序的层状结构,其中烷基尾的有序和结晶同时发生。对于长度为17的较短的烷基尾,没有形成有序结构。这与反向的P4VP /烷基苯酚体系完全不同,在P4VP /烷基苯酚体系中,对于长度为15的烷基尾巴(即十五烷基苯酚),在约10k以下形成有序结构。 55摄氏度,然后在大约50℃下结晶烷基尾部。 20摄氏度。这可能归因于PpHS(分子内)氢键形成的可能性。 (C)2016 Elsevier Ltd.保留所有权利。

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