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两种不同拓扑结构聚合物的单晶到单晶合成

Single-Crystal-to-Single-Crystal Synthesis of a Polymer in Two Distinct Topologies.

作者信息

Pathan Javed R, Balan Haripriya, Das Kaustav, Reddy C Malla, Sureshan Kana M

机构信息

School of Chemistry, Indian Institute of Science Education and Research, Thiruvananthapuram, Kerala, 695551, India.

Department of Chemical Sciences, Indian Institute of Science Education and Research, Kolkata, West Bengal, 741246, India.

出版信息

Angew Chem Int Ed Engl. 2025 Apr 7;64(15):e202500646. doi: 10.1002/anie.202500646. Epub 2025 Feb 11.

Abstract

A squaramide-based monomer, designed for topochemical azide-alkyne cycloaddition (TAAC) polymerization, crystallizes as two polymorphs, M1 and M2, both having crystal packing suitable for topochemical polymerization. The hydrogen-bonding between squaramide units bias the molecular organization in both the polymorphs. 3D packing of H-bonded stacks of monomer lead to juxtaposition of azide and alkyne units of adjacent molecules in a transition-state-like arrangement for their regiospecific cycloaddition reaction. The monomers are arranged as supramolecular sheets and supramolecular helices in polymorph M1 and M2 respectively. Both the polymorphs undergo slow and spontaneous regiospecific TAAC polymerization at room temperature, but react quickly at higher temperatures, resulting in 1,4-traizolyl-linked polymer, with distinct mechanical responses. Upon heating, single crystals of polymorph M1 show expansion followed by contraction without any permanent dimensional change, whereas crystals of polymorph M2 undergo splitting. At moderate temperatures, both the polymorphs undergo single-crystal-to-single-crystal (SCSC) polymerization, resulting in two polymer-polymorphs with distinct topologies that can be studied at atomic resolution by single-crystal X-ray crystallography. The polymorph M1 reacts to polymer P1 with β-sheet-like topology, and polymorph M2 reacts to polymer P2 having polymer chains of helical conformation. Nanoindentation experiments with crystals of these polymers revealed their distinct mechanical properties.

摘要

一种基于方酰胺的单体,专为拓扑化学叠氮化物-炔烃环加成(TAAC)聚合而设计,结晶为两种多晶型物M1和M2,二者都具有适合拓扑化学聚合的晶体堆积。方酰胺单元之间的氢键作用使两种多晶型物中的分子排列产生偏向。单体的氢键堆叠的三维堆积导致相邻分子的叠氮化物和炔烃单元以类似过渡态的排列并置,以进行区域特异性环加成反应。在多晶型物M1和M2中,单体分别排列成超分子片层和超分子螺旋。两种多晶型物在室温下都经历缓慢且自发的区域特异性TAAC聚合,但在较高温度下反应迅速,生成具有独特机械响应的1,4-三唑基连接的聚合物。加热时,多晶型物M1的单晶显示出先膨胀后收缩,且没有任何永久性尺寸变化,而多晶型物M2的晶体则会发生分裂。在中等温度下,两种多晶型物都经历单晶到单晶(SCSC)聚合,生成具有不同拓扑结构的两种聚合物多晶型物,可通过单晶X射线晶体学在原子分辨率下进行研究。多晶型物M1反应生成具有β-片状拓扑结构的聚合物P1,多晶型物M2反应生成具有螺旋构象聚合物链的聚合物P2。对这些聚合物晶体进行的纳米压痕实验揭示了它们独特的机械性能。

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