镧系元素
八面体
配体(生物化学)
发光
配位几何学
聚合物
配位聚合物
材料科学
放松(心理学)
结晶
三角双锥分子几何
八面体分子几何学
协调球
五角双锥分子几何
激发
分子内力
化学
结晶学
化学物理
晶体结构
协调数
配位复合体
卤化物
磁化率
棱镜
离子
作者
Xiang-Tao Dong,Ting Zhu,Rongyan Zhang,Guo Peng,Lijun Fu,Xiao‐Ming Ren
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:54 (45): 16805-16813
被引量:3
摘要
O (3). The structural dimensionality of complexes 1-3 varies from one-dimensional (1D) to three-dimensional (3D) depending on the reaction conditions and crystallization methods. Complexes 1 and 3 consist of a 1D polymeric chain and a 3D framework, respectively, formed from seven-coordinate Dy(III) ions and TTP linkers. The Dy(III) ion in complex 1 adopts an intermediate geometry between a capped trigonal prism and a capped octahedron, while that in complex 3 shows a pentagonal bipyramidal geometry. Complex 2 exhibits a two-dimensional (2D) network, where the Dy(III) ion adopts a six-coordinate octahedral coordination geometry. Magnetic studies revealed that complex 1 exhibits slow magnetic relaxation at a zero static field, while this behavior in complexes 2 and 3 is field-induced, occurring only under a static field. Solid-state luminescence investigations demonstrated that complexes 1-3 exhibit excitation-dependent emissions, with their emission color tunable from yellow to white across different excitation wavelengths. The magnetic properties and yellow emissions of the products are determined by the coordination environments and geometries around the Dy(III) ions.
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