中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Supramolecular topology design of silver(I) and copper(II) coordination polymers through a new semi-rigid sulfonyl ligand with different anion templates

文献类型:期刊论文

作者Qi, Zhaoxian1,2; Zhao, Li1; Li, Zhiwen2,3; Tian, Shanli2; Xiao, Qian1; Deng, Yuheng1; Zhang, Jiangwei2; Li, Gao2; Wan, Chongqing1
刊名DALTON TRANSACTIONS
出版日期2019-05-28
卷号48期号:20页码:6730-6737
ISSN号1477-9226
DOI10.1039/c9dt00257j
通讯作者Zhang, Jiangwei(jwzhang@dicp.ac.cn)
英文摘要A series of metal organic coordination polymers (MOCPs) of silver(I) and copper(II) coordinated with a novel multifunctional semi-rigid sulfonyl ligand with different anion templates and oxidation states were designed for the first time. In addition, their atomically precise molecular structure was determined by single crystal X-ray diffraction analysis. In comparison, the topology of silver(I)-based MOCPs is affected significantly by different anion templates. The coordination modes are quite different with the anions varying: linear for ClO4-, trilateral for CO2CF3-, and tetrahedral for CO2C2F5-. Due to the difference of electron configurations between Ag(I) and Cu(II), the coordinated configuration of the metal center is also different. While the coordinated configuration of Cu(II) center tends to be placed in an octahedron. Furthermore, for the copper(II) MOCPs, the oxidation state of the L ligand also plays an important role. When the N atoms in L were oxidized, the coordination mode of Cu(II) became tetrahedral with Cu(II) stuck on the bottom of the conventional octahedral mode. In general, it is an effective and controllable strategy to mediate the coordination mode and aggregation of supramolecular assembly-based MOCPs through the combination of a multifunctional organic ligand and its corresponding oxidation state design; elaborate metallic species and electron configuration selection; and suitable anion template introduction to generate multiform and hierarchical non-covalent bond interactions including pi-pi interactions and hydrogen bond formation that afford their coordination mode diversity.
WOS关键词COMPLEXES ; LUMINESCENCE ; FRAMEWORKS
资助项目National Natural Science Foundation of China[21371123] ; National Natural Science Foundation of China[21701168] ; Liaoning Natural Science Foundation[20170540897] ; Liaoning Natural Science Foundation[20180510050] ; Natural Science Foundation of Beijing Municipality[2172014] ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter[20160009] ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University
WOS研究方向Chemistry
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000472452900042
资助机构National Natural Science Foundation of China ; National Natural Science Foundation of China ; Liaoning Natural Science Foundation ; Liaoning Natural Science Foundation ; Natural Science Foundation of Beijing Municipality ; Natural Science Foundation of Beijing Municipality ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; Liaoning Natural Science Foundation ; Liaoning Natural Science Foundation ; Natural Science Foundation of Beijing Municipality ; Natural Science Foundation of Beijing Municipality ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; Liaoning Natural Science Foundation ; Liaoning Natural Science Foundation ; Natural Science Foundation of Beijing Municipality ; Natural Science Foundation of Beijing Municipality ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; Liaoning Natural Science Foundation ; Liaoning Natural Science Foundation ; Natural Science Foundation of Beijing Municipality ; Natural Science Foundation of Beijing Municipality ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; State Key Laboratory of Structural Chemistry at Fujian Institute of Research on the Structure of Matter ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University ; Key Laboratory of Life Organic Phosphorus Chemistry and Chemical Biology, Ministry of Education, Tsinghua University
源URL[http://cas-ir.dicp.ac.cn/handle/321008/176012]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Zhang, Jiangwei
作者单位1.Capital Normal Univ, Dept Chem, Beijing Key Lab Opt Mat & Photon Devices, Beijing 100048, Peoples R China
2.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
3.Liaoning Normal Univ, Dept Chem & Chem Engn, Dalian 116029, Peoples R China
推荐引用方式
GB/T 7714
Qi, Zhaoxian,Zhao, Li,Li, Zhiwen,et al. Supramolecular topology design of silver(I) and copper(II) coordination polymers through a new semi-rigid sulfonyl ligand with different anion templates[J]. DALTON TRANSACTIONS,2019,48(20):6730-6737.
APA Qi, Zhaoxian.,Zhao, Li.,Li, Zhiwen.,Tian, Shanli.,Xiao, Qian.,...&Wan, Chongqing.(2019).Supramolecular topology design of silver(I) and copper(II) coordination polymers through a new semi-rigid sulfonyl ligand with different anion templates.DALTON TRANSACTIONS,48(20),6730-6737.
MLA Qi, Zhaoxian,et al."Supramolecular topology design of silver(I) and copper(II) coordination polymers through a new semi-rigid sulfonyl ligand with different anion templates".DALTON TRANSACTIONS 48.20(2019):6730-6737.

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来源:大连化学物理研究所

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