Thermal curing mechanisms and cross-linking network structure of a novel silicon-containing arylacetylene resin with 2,7-diethynylnaphthalene unit

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of molecular graphics & modelling Pub Date : 2024-06-06 DOI:10.1016/j.jmgm.2024.108811
Hui Li, Lei Yang, Zijian Sun, Weihua Zhu
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Abstract

Silicon-containing arylacetylene resin and its composites have attracted great interest as emerging heat-resistant materials, but their curing mechanisms and products are still elusive. In this work, the influences of the terminal and inner acetylenes on the curing mechanisms of silicon-containing arylacetylene resin with 2,7-diethynylnaphthalene were first identified by density functional theory. Two reaction pathways were proposed and their products include polyenes, anthracene dimers, and benzene trimers. To gain a distinct observation of the cross-linking process, molecular dynamics simulations were used to construct a cross-linking polymerization model. The effects of the temperature on the cured structure were investigated by analyzing the characteristics of the cross-linked network. As expected, higher curing temperature will make the larger proportion of polyene chain and aromatic ring in the terminal alkyne−terminal alkyne route, meanwhile, for the inner alkyne−inner alkyne route, the short chains and a small amount of aromatic rings are major productions. Overall, our cross-linking method may provide an unique guidance for studying the cured structure of other thermosetting resins.

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具有 2,7 二甲基萘单元的新型含硅芳基乙炔树脂的热固化机理和交联网络结构
含硅芳基乙炔树脂及其复合材料作为一种新兴的耐热材料引起了人们的极大兴趣,但其固化机理和产物至今仍难以确定。本研究通过密度泛函理论首次确定了末端和内部乙炔基对含硅芳基乙炔树脂与 2,7-二乙炔基萘固化机理的影响。提出了两种反应途径,其产物包括多烯、蒽二聚物和苯三聚物。为了对交联过程有一个清晰的观察,我们利用分子动力学模拟构建了一个交联聚合模型。通过分析交联网络的特征,研究了温度对固化结构的影响。结果表明,固化温度越高,在端炔-端炔路线中多烯链和芳香环的比例越大,而在内炔-内炔路线中,短链和少量芳香环是主要产物。总之,我们的交联方法可为研究其他热固性树脂的固化结构提供独特的指导。
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来源期刊
Journal of molecular graphics & modelling
Journal of molecular graphics & modelling 生物-计算机:跨学科应用
CiteScore
5.50
自引率
6.90%
发文量
216
审稿时长
35 days
期刊介绍: The Journal of Molecular Graphics and Modelling is devoted to the publication of papers on the uses of computers in theoretical investigations of molecular structure, function, interaction, and design. The scope of the journal includes all aspects of molecular modeling and computational chemistry, including, for instance, the study of molecular shape and properties, molecular simulations, protein and polymer engineering, drug design, materials design, structure-activity and structure-property relationships, database mining, and compound library design. As a primary research journal, JMGM seeks to bring new knowledge to the attention of our readers. As such, submissions to the journal need to not only report results, but must draw conclusions and explore implications of the work presented. Authors are strongly encouraged to bear this in mind when preparing manuscripts. Routine applications of standard modelling approaches, providing only very limited new scientific insight, will not meet our criteria for publication. Reproducibility of reported calculations is an important issue. Wherever possible, we urge authors to enhance their papers with Supplementary Data, for example, in QSAR studies machine-readable versions of molecular datasets or in the development of new force-field parameters versions of the topology and force field parameter files. Routine applications of existing methods that do not lead to genuinely new insight will not be considered.
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