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手性嵌段共聚物自组装形成的新型纳米结构。

Novel nanostructures from self-assembly of chiral block copolymers.

作者信息

Ho Rong-Ming, Chen Chun-Ku, Chiang Yeo-Wan

机构信息

Department of Chemical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

Macromol Rapid Commun. 2009 Sep 1;30(17):1439-56. doi: 10.1002/marc.200900181. Epub 2009 Jun 16.

Abstract

A diblock copolymer system constituting both achiral and chiral blocks, polystyrene-block-poly(L-lactide) (PS-PLLA), was designed for the examination of chiral effects on the self-assembly of block copolymers (BCPs). A unique phase with three-dimensional hexagonally packed PLLA helices in PS matrix, a helical phase (H*), can be obtained from the self-assembly of PS-rich PS-PLLA with volume fraction of PLLA f PLLAv = 0.34, whereas no such phase was found in racemic polystyrene-block-poly(D.L-lactide) (PS-PLA) BCPs. Moreover, various interesting crystalline PS-PLLA nanostructures can be obtained by controlling the crystallization temperature of PLLA (T(c,PLLA) ), leading to the formation of crystalline helices (PLLA crystallization directed by helical confined microdomain) and crystalline cylinders (phase transformation of helical nanostructure dictated by crystallization) when T(c,PLLA)  < T(g,PS) (the glass transition temperature of PS) and T(c,PLLA)  ≧ T(g,PS) , respectively. As a result, a spring-like behavior of the helical nanostructure can be driven by crystallization so as to dictate the transformation (i.e., stretching) of helices and to result in crystalline cylinders. For PS-PLLA with PLLA-rich fraction (f PLLAv = 0.65), another unique phase, a hexagonally packed core-shell cylinder phase with helical sense (CS*), in which the PS microdomains appear as shells and PLLA microdomains appear as matrix and cores, can be found in the self-assembly of PLLA-rich PS-PLLA BCPs. The formation of those novel phases: helix and core-shell cylinder is attributed to the chiral effect on the self-assembly of BCPs, so we named this PS-PLLA BCP as chiral BCP (BCP*). For potential applications of those materials, the spring-like behavior with thermal reversibility might provide a method for the design of switchable nanodevices, such as nanoscale actuators. In addition, the PLLA blocks can be hydrolyzed. After hydrolysis, helical nanoporous PS bulk and PS tubular texture can be obtained and used as templates for the formation of nanocomposites.

摘要

设计了一种由非手性和手性嵌段组成的双嵌段共聚物体系,即聚苯乙烯-嵌段-聚(L-丙交酯)(PS-PLLA),用于研究手性对嵌段共聚物(BCP)自组装的影响。从富含聚苯乙烯且聚丙交酯体积分数f PLLAv = 0.34的PS-PLLA自组装中可获得一种独特的相,即在PS基质中具有三维六方堆积的PLLA螺旋的螺旋相(H*),而在消旋聚苯乙烯-嵌段-聚(D,L-丙交酯)(PS-PLA)BCP中未发现这种相。此外,通过控制聚丙交酯的结晶温度(T(c,PLLA)),可以获得各种有趣的结晶PS-PLLA纳米结构,当T(c,PLLA)  < T(g,PS)(PS的玻璃化转变温度)时导致形成结晶螺旋(由螺旋受限微区引导的PLLA结晶),当T(c,PLLA)  ≧ T(g,PS)时导致形成结晶圆柱体(由结晶决定的螺旋纳米结构的相变)。结果,螺旋纳米结构的弹簧状行为可由结晶驱动,从而决定螺旋的转变(即拉伸)并导致形成结晶圆柱体。对于富含聚丙交酯的部分(f PLLAv = 0.65)的PS-PLLA,在富含PLLA的PS-PLLA BCP自组装中可以发现另一种独特的相,即具有螺旋方向的六方堆积核壳圆柱体相(CS*),其中PS微区表现为壳,PLLA微区表现为基质和核。这些新相(螺旋和核壳圆柱体)的形成归因于手性对BCP自组装的影响,因此我们将这种PS-PLLA BCP命名为手性BCP(BCP*)。对于这些材料的潜在应用,具有热可逆性的弹簧状行为可能为可切换纳米器件(如纳米级致动器)的设计提供一种方法。此外,PLLA嵌段可以水解。水解后,可以获得螺旋纳米多孔PS块体和PS管状结构,并用作形成纳米复合材料的模板。

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