浓缩溶液中致密单链纳米颗粒的合成

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Kairu Qu, Zhenzhong Yang
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引用次数: 0

摘要

虽然大量共价交联的坚固单链纳米颗粒(SCNPs)已经被广泛合成,但它们是稀疏交联的,缺乏对致密度的精确控制。在此,我们提出了一种简单的方法,通过亲本动态SCNPs的共价交联来实现具有可调紧凑性的鲁棒SCNPs。为了证明这一概念,以200 mg/mL的浓度,通过氨基酸特异性相互作用,通过静电介导的聚(N,N-二甲氨基乙基甲基丙烯酸酯)(PDMAEMA)基聚合物的分子内物理交联,大规模合成了动态SCNPs。通过改变交联度和交联剂的间隔长度,动态SCNPs的紧凑性可从稀疏交联到球形状态,其尺度参数在0.57 ~ 0.34之间。通过对动态SCNPs进行共价交联,得到了紧度可调的鲁棒SCNPs。通过使用功能剂和功能材料的优先生长,SCNPs具有明显划分的功能微畴。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis of Compact Single-Chain Nanoparticles in Concentrated Solutions

Synthesis of Compact Single-Chain Nanoparticles in Concentrated Solutions
Although a large family of covalently cross-linked robust single-chain nanoparticles (SCNPs) have been extensively synthesized, they are sparsely cross-linked, lacking precision control of the compactness. Herein, we propose a facile method to achieve robust SCNPs with tunable compactness by covalent cross-linking of the parent dynamic SCNPs. As proof of the concept, the dynamic SCNPs are large-scale synthesized at 200 mg/mL by the electrostatics-mediated intramolecular physical cross-linking of poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA)-based polymers via amino/acid-specific interactions. The compactness of the dynamic SCNPs is greatly tunable from sparsely cross-linked to the globular state with scaling parameters from 0.57 to 0.34 by altering the cross-linking degree and spacer length of the cross-linker. The robust SCNPs with tunable compactness are derived by subsequent covalent cross-linking of the dynamic SCNPs. The SCNPs are featured with functional microdomains distinctly compartmentalized by using functional agents and preferential growth of functional materials thereby.
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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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