首页> 外文期刊>Liquid Crystals: An International Journal in the Field of Anisotropic Fluids >Synthesis and phase structures of combined main-chain/side-chain liquid crystalline polymers with different-number azobenzene moiety in the side-chain based on mesogen-jacketed liquid crystalline polymers
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Synthesis and phase structures of combined main-chain/side-chain liquid crystalline polymers with different-number azobenzene moiety in the side-chain based on mesogen-jacketed liquid crystalline polymers

机译:基于介晶夹层液晶聚合物的侧链中具有不同数目偶氮苯部分的主链/侧链组合液晶聚合物的合成和相结构

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摘要

Three novel combined main-chain/side-chain liquid crystalline polymers with different number of azobenzene mesogens in the side chain per repeating unit have been synthesised. These are poly(2,5-bis{[3-(4′-methoxy-4-oxyhexyloxy azobenzene)benzyl]oxycarbonyl}styrene) (denoted as PABCS), poly(2,5-bis{[3,5-di(4′-methoxy-4-oxyhexyloxy azobenzene)benzyl]oxycarbonyl}styrene) (denoted as PDABCS) and poly (2,5-bis{[3,4,5-tri(4′-methoxy-4-oxyhexyloxy azobenzene)benzyl]oxycarbonyl}styrene) (denoted as PTABCS). The chemical structure of the monomers was confirmed by ~1H NMR and ~(13)C NMR. The structural characterisation of the polymers was performed by ~1H NMR and gel permeation chromatography (GPC), and the phase structures and transitions of the polymers were studied using differential scanning calorimetry (DSC), polarised light microscopy (PLM) and one-dimensional (1D) wide-angle X-ray diffraction (WAXD). The results show that the number of azobenzene mesogens in the side chain per repeating unit in the combined main-chain/side-chain liquid crystalline polymers plays an important role in dominating the phase type preferences, and the polymers exhibit more versatile and intriguing liquid crystalline properties with increasing number of azobenzene mesogens. First, the main chains of PABCS construct a 2D-centred rectangular (Φ_R) scaffold and the packing of azobenzene-containing side chains inside the main-chain scaffold develops smecitc A (SmA)-like structure below isotropic temperature (T_i). Second, with increasing the number of azobenzene mesogens, the main chains of PDABCS develop a 2D-centred rectangular (Φ_R) scaffold at lower temperature and a 2D hexagonal columnar (Φ_H) phase at higher temperature, and the packing of side chains inside the main-chain scaffold undergoes the transition of SmA-like ? isotropic. Third, for PTABCS, the sequence of phase transitions followed is: 2D centred rectangular columnar phase (Φ_R) scaffold of main chain and SmB-like structure of side chain ? 2D centred rectangular columnar phase (Φ_R) scaffold of main chain and SmA-like structure of side chain ? 2D centred rectangular (Φ_R) scaffold of main chain and isotropic side chain ? 2D long-range-ordered hexagonal columnar phase (Φ_H) of main chain and isotropic side chain. The 2D long-range-ordered ΦH phases of the polymers PDABCS and PTABCS still remain before the samples are completely decomposed.
机译:合成了三种新颖的组合的主链/侧链液晶聚合物,每个重复单元的侧链中具有不同数量的偶氮苯液晶元。这些是聚(2,5-双{[3-(4'-甲氧基-4-氧基己氧基偶氮苯)苄基]氧羰基}苯乙烯)(表示为PABCS),聚(2,5-双{[3,5-di (4'-甲氧基-4-氧基己氧基偶氮苯)苄基]氧基羰基}苯乙烯)(表示为PDABCS)和聚(2,5-双{[3,4,5-tri(4'-甲氧基-4-氧基己氧基偶氮苯)苄基]氧羰基}苯乙烯)(表示为PTABCS)。通过〜1 H NMR和〜(13)C NMR确认单体的化学结构。聚合物的结构表征通过〜1H NMR和凝胶渗透色谱(GPC)进行,并使用差示扫描量热法(DSC),偏振光显微镜(PLM)和一维( 1D)广角X射线衍射(WAXD)。结果表明,在组合的主链/侧链液晶聚合物中,每个重复单元的侧链中偶氮苯液晶元的数量在主导相类型偏好中起着重要作用,并且该聚合物表现出更多用途和令人感兴趣的液晶偶氮苯介晶数的增加的性质。首先,PABCS的主链构建一个二维中心的矩形(Φ_R)支架,并且在各向同性温度(T_i)下,主链支架内含偶氮苯的侧链堆积形成了类似smecitc A(SmA)的结构。其次,随着偶氮苯介晶数的增加,PDABCS的主链在较低温度下形成2D中心矩形(Φ_R)支架,在较高温度下形成2D六角形柱状(Φ_H)相,并且主链内的侧链堆积链支架经历了类似SmA的转变?各向同性。第三,对于PTABCS,遵循的相变顺序为:主链的二维中心矩形柱状相(Φ_R)支架和侧链的SmB样结构?主链的二维中心矩形柱状相(Φ_R)支架和侧链的SmA样结构?主链和各向同性侧链的二维居中矩形(Φ_R)支架?主链和各向同性侧链的二维长程六方柱状相(Φ_H)。在样品完全分解之前,聚合物PDABCS和PTABCS的二维远距离ΦH相仍然保留。

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