Cluster-based Magnetic Porous Coordination Polymers

被引:0
|
作者
Xiang Sheng-Chang [1 ]
Wang Xin [1 ]
Hu Sheng-Min [1 ]
Sheng Tian-Lu [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
关键词
magnetism; porosity; coordination polymers; cluster; amino acids; citrate; METAL-ORGANIC FRAMEWORK; HIGH H-2 ADSORPTION; AMINO-ACID; CITRATE COMPLEX; SERIES; CRYSTAL; POLYHEDRA; CHELATION; BEHAVIOR; SOLIDS;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The creation of a porous magnet is a long-sought academic goal since magnetism and porosity are hostile to one another. While long-range magnetic ordering needs spin carriers of short separation through short bridges, porosity relies on the use of extended connecting ligands. Here, we will give a survey of the cluster-based magnetic porous coordination polymers, i.e., 0-D MPCPs, according to their Junctional subunits: (1) nanoporous spin crossover materials with single metal nodes; (2) metal-radical approach with rigid organic radical ligands and single metal nodes; (C) PCPs with rigid organic ligands and metal oligomer nodes; (D) PCPs with metal complex linkers and polymetal cluster nodes; (E) PCPs with organo-polymetal cluster linkers and single metal nodes. The assembly from clusters can provide a reasonable route to resolve the hostility between magnetism and porosity. This assembly's merits are obvious: the pore benefits from the big cluster according to "Scale Chemistry", and the functional framework inherits interesting physical properties from the clusters with a large ground spin S.
引用
收藏
页码:1349 / 1358
页数:10
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