化学
镝
四氢呋喃
八面体
结晶学
卡宾
部分
放松(心理学)
分子
八面体分子几何学
配体(生物化学)
单分子磁体
磁化
配位场理论
立体化学
无机化学
离子
磁场
晶体结构
有机化学
催化作用
溶剂
受体
物理
社会心理学
量子力学
生物化学
心理学
作者
Jérôme Long,Dmitry M. Lyubov,Galina A. Gurina,Yulia V. Nelyubina,Fabrice Salles,Yannick Guari≠,Joulia Larionova≠,Alexander A. Trifonov
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-01-07
卷期号:61 (3): 1264-1269
被引量:9
标识
DOI:10.1021/acs.inorgchem.1c03429
摘要
We report the synthesis, structures, and magnetic investigations of two new octahedral dysprosium complexes, based on the original N-heterocyclic carbene (NHC) tridentate bis(phenoxide) ligand, of the respective formulas mer-[DyL(THF)2Cl] (1) and mer-[DyL(THF)3][BPh4] (2), where L = 1,3-bis(3,5-di-tert-butyl-2-oxidophenyl)-5,5-dimethyl-3,4,5,6-tetrahydropyrimidin-1-ium chloride and THF = tetrahydrofuran. The short Dy-O distances in the axial direction in association with the weak donor ability of the NHC moiety provide a suitable environment for slow relaxation of magnetization, overcoming the previous single-molecule magnets based on NHC ligands.
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