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含 1,3-亚苯基双-((1H-1,2,4-三唑-1-基)甲酮)配体的配位聚合物:合成及 ε-己内酯聚合行为。

Coordination Polymers Containing 1,3-Phenylenebis-((1H-1,2,4-triazol-1-yl)methanone) Ligand: Synthesis and ε-Caprolactone Polymerization Behavior.

机构信息

Department of Chemistry, Universidad de los Andes, Carrera 1 N° 18A-12, Bogotá 111711, Colombia.

Grupo de Química Inorgánica y Materiales Moleculares, Universidad Autonoma de Chile, El Llano Subercaseaux 2801, Santiago 8910060, Chile.

出版信息

Molecules. 2017 Nov 10;22(11):1860. doi: 10.3390/molecules22111860.

Abstract

The reaction of isophthaloyl dichloride with 1-1,2,4-triazole afforded the new ligand 1,3-phenylenebis(1,2,4-triazole-1-yl)methanone (). A series of Co(II), Cu(II), Zn(II) and Ni(II) complexes were synthesized using and then characterized by melting point analysis, elemental analysis, theoretical calculations, thermogravimetric analysis, X-ray powder diffraction, nuclear magnetic resonance, infrared and Raman spectroscopy. Experimental and computational studies predict the formation of coordination polymers (CPs). The cobalt and copper CPs and zinc(II) complex were found to be good initiators for the ring-opening polymerization of ε-caprolactone (CL) under solvent-free conditions. ¹H-NMR analysis showed that the obtained polymers of CL were mainly linear and had terminal hydroxymethylene groups. Differential scanning calorimetry showed that the obtained polycaprolactones had high crystallinity, and TGA showed that they had decomposition temperatures above 400 °C. These results provide insight and guidance for the design of metal complexes with potential applications in the polymerization of CL.

摘要

均苯二酰二氯与 1-(1,2,4-三唑基)-1,2,4-三唑反应得到新配体 1,3-亚苯基双(1,2,4-三唑-1-基)甲酮()。使用 和然后通过熔点分析、元素分析、理论计算、热重分析、X 射线粉末衍射、核磁共振、红外和拉曼光谱进行了一系列 Co(II)、Cu(II)、Zn(II)和 Ni(II)配合物的合成。实验和计算研究预测了配位聚合物 (CP) 的形成。发现钴和铜的 CPs 和锌(II)配合物在无溶剂条件下是ε-己内酯 (CL) 开环聚合的良好引发剂。¹H-NMR 分析表明,得到的 CL 聚合物主要为线性,具有末端羟甲基基团。差示扫描量热法表明,得到的聚己内酯具有高结晶度,热重分析表明其分解温度高于 400°C。这些结果为具有潜在应用于 CL 聚合的金属配合物的设计提供了见解和指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a5/6150338/f3adfad34fdf/molecules-22-01860-sch001.jpg

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