具有不同间隔长度的楔形侧链液晶聚合物的层次动力学和相变

IF 5.7 1区 化学 Q1 POLYMER SCIENCE
Minghe Sun,Yining Fan,Pingchuan Sun,Shuang Yang,Er-Qiang Chen
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引用次数: 0

摘要

作为一类重要的接枝聚合物,含有各向异性介生基团的侧链液晶聚合物(SCLCPs)具有复杂的分子动力学,与层次结构演化密切相关。在这项研究中,我们使用各种表征技术,研究了一系列楔形sclcp的相结构和粘弹性行为,表示为CxBP (x = 1,3,7),其中x是连接楔形介源侧基到聚降冰片烯骨架的间隔中亚甲基单位的数量。cxbp形成六方柱状相(ColH),多链超分子柱是主链和侧链微相分离产生的基本构建块。从各向同性状态冷却后,cxbp在剪切模量分别为104、105、107和108 Pa的4个不同阶段(I-IV)表现出独特的多步增长,并被3个弛豫/转变过程(α、β、γ)分开。当接近-100°C时,δ弛豫进一步将模量提高到~ 109 Pa。α-和γ-过程对应于一阶转变:各向同性到colh的转变分别在~ 90°C和侧链烷基尾部的部分有序在~ 0°C。值得注意的是,β-过程主要是非合作弛豫,遵循阿伦尼乌斯行为,活化能为~ 300 kJ/mol,归因于侧链上的介质运动。这种运动的冻结使ColH从“移动”状态转变为“中质阻滞”状态,从阶段II到阶段III的剪切模量增加了2个数量级。我们发现较长的间隔可以降低β弛豫温度。C1BP以单个亚甲基为间隔层,表现出β-弛豫与α-过程部分重叠。将间隔长度延长至三个或更多亚甲基单元(C3BP, C7BP),可以使主链和侧链充分动态解耦,产生更宽的II级剪切模量为105 Pa。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hierarchical Dynamics and Phase Transitions in Wedge-Shaped Side-Chain Liquid Crystalline Polymers with Varying Spacer Lengths

Hierarchical Dynamics and Phase Transitions in Wedge-Shaped Side-Chain Liquid Crystalline Polymers with Varying Spacer Lengths
As an important class of graft polymers, side-chain liquid crystalline polymers (SCLCPs) containing anisotropic mesogenic groups exhibit complex molecular dynamics that are closely coupled with hierarchical structural evolution. In this study, using various characterization techniques, we investigate the phase structures and viscoelastic behavior of a series of wedge-shaped SCLCPs, denoted as CxBP (x = 1, 3, 7), where x is the number of methylene units in the spacer linking the wedge-shaped mesogenic side group to the polynorbornene backbone. CxBPs form a hexagonal columnar phase (ColH), with multichain supramolecular columns serving as the basic building block arising from microphase separation of the main and side chains. Upon cooling from the isotropic state, CxBPs show unique multistep increases in modulus through four distinct stages (I–IV) with shear moduli of 104, 105, 107, and 108 Pa, respectively, separated by three relaxation/transition processes (α, β, γ). When approaching to –100 °C, a δ-relaxation further raises the modulus to ∼109 Pa. The α- and γ-processes correspond to first-order transitions: the isotropic-to-ColH transition at ∼90 °C and partial ordering of the side-chain alkyl tails at ∼0 °C, respectively. Notably, the β-process is a predominantly noncooperative relaxation following Arrhenius behavior with an activation energy of ∼300 kJ/mol, attributed to the motion of mesogens on the side chains. Freezing of this motion transforms the ColH from a “mobile” to a “mesogen-arrested” state, increasing the shear modulus by 2 orders of magnitude from stage II to stage III. We find that a longer spacer lowers the β-relaxation temperature. With a single methylene unit as the spacer, C1BP shows β-relaxation partially overlapping with the α-process. Extending the spacer length to three or more methylene units (C3BP, C7BP) enables sufficient dynamic decoupling of the main and side chains, yielding a wider stage II with a shear modulus of 105 Pa.
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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