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首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Effects of the architecture and environment on polymeric molecular assemblies of novel amphiphilic diblock copolynorbornenes with narrow polydispersity via living ring-opening metathesis polymerization
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Effects of the architecture and environment on polymeric molecular assemblies of novel amphiphilic diblock copolynorbornenes with narrow polydispersity via living ring-opening metathesis polymerization

机译:结构和环境对新型两亲性二嵌段共聚降冰片烯通过活开环易位聚合反应的影响

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摘要

Diblock copolymers of 5-(methylphthalimide)bicyclo[2.2.1]hept-2-ene (NBMPI) and 1,5-cyclooctadiene were synthesized by living ring-opening metathesis polymerization with a well-defined catalyst {RuCl2(CHPh)[P(C6H11)(3)](2)}. Unhydrogenated diblock copolymers showed two glass transitions due to poly(NBMPI) and polybutadiene segments, such as two glass-transition temperatures at -86.5 and 115.3 degrees C for poly1a and -87.2 and 115.3 degrees C for poly1b. However, only one melting temperature could be observed for hydrogenated copolymers, such as 119.8 degrees C for poly2a and 121.7 degrees C for poly2b. The unhydrogenated diblock copolymer with the longer poly(NBMPI) chain (poly1a; temperature at 10% mass loss = 400 degrees C) exhibited better thermal stability than the one with the shorter poly(NBMPI) chain (poly1b; temperature at 10% mass loss = 385 degrees C). Two kinds of hydrogenated diblock copolymers, poly2a and poly2b, exhibited relatively poor solubility but better thermal stability than unhydrogenated diblock copolymers because of the polyethylene segments. Poly[(hydrochloride quaternized 2-norbornene-5-methyleneamine)-b-butadiene]-1 (poly3a) was obtained after the hydrolysis and quaternization of poly1a. Dynamic light scattering measurements indicated that the hydrodynamic diameters of the cationic copolymer (poly3a) in water (hydrodynamic diameter = 1580 nm without salt), methanol/water (4/96 v/v; hydrodynamic diameter = 1500 nm without salt), and tetrahydrofuran/water (4/96 v/v; hydrodynamic diameter = 1200 nm without salt) decreased with increasing salt (NaCl) concentration. The effect of temperature on the hydrodynamic diameter of hydrophobically modified poly3a was also studied. The inflection point of the hydrodynamic diameter of poly3a was observed at various polymer concentrations around 30 degrees C. The critical micelle concentration of hydrophobically modified poly3a was observed at 0.018 g dL(-1). (c) 2006 Wiley Periodicals, Inc.
机译:通过明确定义的催化剂{RuCl2(CHPh)[P]进行活泼的开环复分解聚合反应,合成了5-(甲基邻苯二甲酰亚胺)双环[2.2.1]庚-2-烯(NBMPI)和1,5-环辛二烯的二嵌段共聚物。 (C6H11)(3)](2)}。由于聚(NBMPI)和聚丁二烯链段,未氢化的二嵌段共聚物显示出两个玻璃化转变,例如,对于poly1a,两个玻璃化转变温度分别为-86.5和115.3℃,对于poly1b则为-87.2和115.3℃。但是,对于氢化共聚物只能观察到一个熔融温度,例如对于poly2a为119.8摄氏度,对于poly2b为121.7摄氏度。具有更长的聚(NBMPI)链的未氢化二嵌段共聚物(poly1a; 10%质量损失时的温度= 400摄氏度)表现出比具有较短的poly(NBMPI)链较短的聚合物(poly1b;温度为10%质量损失的温度)更好的热稳定性。 = 385摄氏度)。两种氢化的二嵌段共聚物,poly2a和poly2b,由于聚乙烯的链段,与未氢化的二嵌段共聚物相比,具有相对较差的溶解度,但热稳定性更好。将poly1a水解和季铵化后,得到聚[(盐酸盐季铵化的2-降冰片烯-5-亚甲基胺)-b-丁二烯] -1(poly3a)。动态光散射测量表明,阳离子共聚物(poly3a)在水中的流体力学直径(无盐的流体力学直径= 1580 nm),甲醇/水(4/96 v / v;在没有盐的流体动力学直径= 1500 nm)和四氢呋喃中盐(NaCl)浓度增加,水/水(4/96 v / v;流体动力学直径= 1200 nm,无盐)降低。还研究了温度对疏水改性的poly3a的流体力学直径的影响。在大约30摄氏度的各种聚合物浓度下观察到了poly3a流体力学直径的拐点。在0.018 g dL(-1)处观察到疏水改性的poly3a的临界胶束浓度。 (c)2006年Wiley Periodicals,Inc.

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