Modulating Static and Dynamic Magnetizations of Ytterbium(III) Coordination Polymers by Light-Induced Radicals

被引:0
|
作者
Gou, Xiaoshuang [1 ,2 ]
Wu, Yuewei [1 ,2 ]
Wen, Hanqi [1 ]
Li, Liang [1 ,2 ]
Lan, Wenlong [1 ,2 ]
Liu, Ning [1 ,2 ]
Zhang, Shiqi [1 ,2 ]
Ungur, Liviu [3 ]
Cheng, Peng [1 ,2 ]
Shi, Wei [1 ,2 ]
机构
[1] Nankai Univ, Frontiers Sci Ctr New Organ Matter, Key Lab Adv Energy Mat Chem, MOE, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Chem, State Key Lab Adv Chem Power Sources, Tianjin 300071, Peoples R China
[3] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
来源
CCS CHEMISTRY | 2025年
基金
中国国家自然科学基金;
关键词
two-dimensional coordination polymers; ytterbium complexes; photomagnetism; singlemolecule magnet; magnetization dynamics; MOLECULE MAGNET BEHAVIOR; NEAR-INFRARED FLUORESCENCE; SINGLE-ION MAGNETS; ANISOTROPY; COMPLEXES; BARRIER;
D O I
10.31635/ccschem.024.202404999
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Light-induced transformation from diamagnetic ligand to paramagnetic radical offers a unique approach to modulating the magnetization dynamics of magnetic compounds. In this study, we present a two-dimensional Yb(III) coordination polymer 1 and its Y(III)-diluted analog 1@Y, along with their lightinduced radical forms, 1a and 1a@Y. Due to the presence of light-induced radicals, the magnetic susceptibility properties (chi MT values) of 1a and 1a@Y featured remarkable 82.3% and 88.9% enhancements, respectively, at room temperature, compared with those of 1 and 1@Y, and were accompanied by an unexpected increase in the effective energy barrier for magnetization dynamics. The magnetization dynamics of 1 and 1a involved both Orbach and Raman processes, while 1@Y and 1a@Y exhibited two Raman processes, indicating that the Orbach process that occurred in 1 and 1a was mainly attributed to the magnetic coupling between Yb(III) ions. This work showcases the potential of light-induced radical transformation for tuning both the static and dynamic magnetic properties of lanthanide coordination polymers.
引用
收藏
页数:9
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