{"title":"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","authors":"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","doi":"10.1002/zaac.202400020","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"68 16","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1002/zaac.202400020\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":23934,\"journal\":{\"name\":\"Zeitschrift für anorganische und allgemeine Chemie\",\"volume\":\"68 16\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift für anorganische und allgemeine Chemie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/zaac.202400020\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für anorganische und allgemeine Chemie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/zaac.202400020","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.