金属离子和金属配体比调控构建 Cu(II) 和 Co(II) 配位聚合物作为 L-乳内酯开环聚合的高效催化剂

Jin-Xia Tao, Mei-Jun Wei, F. Tian, Zhen-Xiang Xia, Kun-Lin Huang, Jun-Feng Qian, Ming-Yang He, Sheng-Chun Chen, Qun Chen
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引用次数: 0

摘要

5Fbtx}n(2)和[Co2(NDC)2(Fbtx)]n(3),是在水热反应和微波辅助反应条件下,采用刚性1,4-萘二甲酸(H2NDC)和柔性双(1,2,4-三唑-1-基甲基)-2,3,5,6-四氟苯(Fbtx)的酸碱混合配体合成的。单晶结构分析表明,化合物 1 和 2 均呈现二维(2D)层状结构,而化合物 3 则具有三维(3D)复杂框架。金属离子的几何形状从方形金字塔(1 和 3)到扭曲八面体(2)不等。拓扑研究表明,化合物 1 和 2 暴露出常见的 4 连接 44-sql 网,而化合物 3 则形成了新颖的 4,5 连接网,其点符号为 (43-62-7)(43-64-72-8)。研究了这三种配合物对 L-内酰胺无溶剂开环聚合反应的催化性能。结果表明,具有配位不饱和钴(II)位点的化合物 3 表现出极高的活性,得到的聚合物分子量也很高。此外,复合物 3 催化剂可以循环使用多达五次,并保留催化活性和晶体结构。
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Metal Ion and Metal‐to‐Ligand Ratio Regulated Construction of Cu(II) and Co(II) Coordination Polymers as Efficient Catalysts for Ring‐Opening Polymerization of L‐Lactide
Three new coordination polymers (CPs), {[Cu(NDC)(Fbtx)(H2O)]·1.5H2O}n (1), {[Co(NDC)(Fbtx)(H2O)2]·0.5Fbtx}n (2), and [Co2(NDC)2(Fbtx)]n (3), were synthesized by employing acid‐base mixed ligands of rigid 1,4‐naphthalenedicarboxylic acid (H2NDC) and flexible bis(1,2,4‐triazole‐1‐ylmethyl)‐2,3,5,6‐tetrafluorobenzene (Fbtx) under both hydrothermal and microwave‐assisted reaction conditions. Single‐crystal structure analysis establishted that both compounds 1 and 2 exhibit two‐dimensional (2D) layered structures, while compound 3 features a three‐dimensional (3D) complicated framework. The geometries of metal ions vary from square pyramidal (in 1 and 3) to distorted octahedral (in 2). Topological strudy showed that compounds 1 and 2 have exposed common 4‐connected 44‐sql net, while compound 3 has made a novel 4,5‐connected net with point symbol of (43·62·7)(43·64·72·8). The catalytic performance of the three complexes for the solvent‐free ring‐opening polymerization of L‐lactide has been investigated. The results indicated that compound 3 with coordinatively unsaturated cobalt(II) sites showed very high activity and the molecular weight of the polymer obtained was also high. Moreover, the complex 3 catalyst could be recycled up to five times with the retention of both catalytic activity and crystal structure.
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