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超分子共聚物:理论建模揭示的结构和组成。

Supramolecular Copolymers: Structure and Composition Revealed by Theoretical Modeling.

机构信息

Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology , P.O. Box 513, 5600 MB Eindhoven, The Netherlands.

Institute for Complex Molecular Systems, Eindhoven University of Technology , P.O. Box 513, 5600 MB Eindhoven, The Netherlands.

出版信息

J Am Chem Soc. 2017 May 24;139(20):7036-7044. doi: 10.1021/jacs.7b02835. Epub 2017 May 16.

Abstract

Supramolecular copolymers, non-covalent analogues of synthetic copolymers, constitute a new and promising class of polymers. In contrast to their covalent counterparts, the details of their mechanism of formation, as well as the factors determining their composition and length, are still poorly understood. Here, the supramolecular copolymerization between two slightly structurally different benzene-1,3,5-tricarboxamide (BTA) monomers functionalized with either oligodimethylsiloxane (oDMSi) or alkyl side chains is unraveled by combining experimental and theoretical approaches. By applying the "sergeant-and-soldiers" approach using circular dichroism (CD) experiments, we are able to obtain detailed insights into the structure and composition of these supramolecular copolymers. Moreover, we observe an unexpected chiral induction upon mixing two independently CD-silent solutions of the achiral (soldier) and chiral (sergeant) monomers. We find that the subtle differences in the chemical structure of the two monomers impact their homopolymerization mechanism: whereas alkyl-BTAs cooperatively self-assemble, oDMSi-BTAs self-assemble in an isodesmic manner. The effect of these mechanistic differences in the supramolecular copolymerization process is investigated as a function of the composition of the two monomers and explicitly rationalized by mathematical modeling. The results show that, at low fractions of oDMSi-BTA sergeants (<10 mol%), the polymerization process is cooperative and the supramolecular helicity is biased toward the helical preference of the sergeant. However, at higher fractions of oDMSi-BTA sergeant (>25 mol%), the isodesmic assembly of the increasing amounts of sergeant becomes more dominant, and different species start to coexist in the copolymerization process. The analysis of the experimental data with a newly developed theoretical model allows us to quantify the thermodynamic parameters, the distribution of different species, and the compositions and stack lengths of the formed supramolecular copolymers existing at various feed ratios of the two monomers.

摘要

超分子共聚物是合成共聚物的非共价类似物,构成了一类新的、有前途的聚合物。与它们的共价类似物相比,其形成机制的细节以及决定其组成和长度的因素仍了解甚少。在这里,通过结合实验和理论方法,揭示了两个结构略有不同的苯-1,3,5-三甲酰胺(BTA)单体之间的超分子共聚反应,这两个单体分别用寡二甲基硅氧烷(oDMSi)或烷基侧链官能化。通过应用圆二色性(CD)实验的“警官与士兵”方法,我们能够深入了解这些超分子共聚物的结构和组成。此外,我们观察到在混合两种独立的、无 CD 信号的手性(警官)和非手性(士兵)单体溶液时,会出现意想不到的手性诱导。我们发现,两个单体的化学结构的细微差异会影响它们的均聚物形成机制:烷基-BTAs 协同自组装,而 oDMSi-BTAs 则以等摩尔方式自组装。研究了这两种单体在超分子共聚过程中的机制差异对手性诱导的影响,并通过数学建模进行了明确的合理化解释。结果表明,在 oDMSi-BTA 警官的比例较低(<10 mol%)时,聚合过程是协同的,超分子螺旋性偏向于警官的螺旋偏好。然而,当 oDMSi-BTA 警官的比例较高(>25 mol%)时,越来越多的警官的等摩尔组装变得更为主导,并且在共聚过程中开始共存不同的物种。通过用新开发的理论模型对实验数据进行分析,我们可以量化热力学参数、不同物种的分布以及在两种单体的不同进料比下形成的超分子共聚物的组成和堆积长度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1c/5445503/3eda8bbd16c4/ja-2017-02835q_0009.jpg

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