钴
激进的
分子内力
咪唑
化学
配体(生物化学)
配位复合体
反铁磁性
配位聚合物
接受者
结晶学
水溶液中的金属离子
顺磁性
光化学
离子
金属
立体化学
晶体结构
无机化学
有机化学
物理
受体
量子力学
生物化学
凝聚态物理
作者
Xudong Hou,Giang Truong Nguyen,Tingting Xu,Haipeng Wei,Tun Seng Herng,Gui‐Fei Huo,Dingguan Wang,Jun Ding,Shaofei Wu,Liviu Ungur,Jishan Wu
标识
DOI:10.1002/chem.202200687
摘要
The incorporation of organic radicals into coordination polymers was considered as a promising strategy to promote metal-ligand exchange interactions, but there are only a very limited number of stable organic radical-based ligands that can serve well such a purpose. Herein, we report two new tris(2,4,6-trichlorophenyl)methyl (TTM) radical-based ligands L1 and L2 with two and three imidazole substituents, respectively. The imidazole unit serves as a coordination site and it can also stabilize the TTM radical by intramolecular donor-acceptor interaction. Coordination of L1 and L2 with cobalt(II) ions gave the corresponding one- (CoCP-1) and two-dimensional (CoCP-2) coordination polymers, the structures of which were confirmed by X-ray crystallographic analysis. Magnetic measurements and theoretical calculations suggest antiferromagnetic coupling between the paramagnetic cobalt(II) ions and the radical ligands. Our study provides a rational design for stable organic radical-based ligands and further demonstrated the feasibility of a metal-radical approach toward magnetic materials.
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