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将多金属氧酸盐整合到具有五角双锥对称性的基于Dy(III)的单分子磁体中。

Integrating Polyoxometalate into Dy(III)-based Single-molecule Magnets with Pentagonal Bipyramidal Symmetry.

作者信息

Kong Hui, Ruan Ze-Yu, Chen Yan-Cong, Deng Wei, Liao Pei-Yu, Wu Si-Guo, Tong Ming-Liang

机构信息

Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, IGCME, GBRCE for Functional Molecular Engineering, Sun Yat-Sen University, Guangzhou 510275, China.

出版信息

Inorg Chem. 2024 Aug 26;63(34):15964-15972. doi: 10.1021/acs.inorgchem.4c02340. Epub 2024 Aug 15.

Abstract

Polyoxometalates (POMs) with various coordination fashions are versatile ligands for constructing single-ion magnets (SIMs), but enforcing POM-SIMs with a specific geometry remains a synthetic challenge. Herein, we synthesized a POM-cocrystallized Dy-SIM [Dy(OPPh)(HO)][PWO]·4EtOH () and a POM-ligated Dy-SIM [{Dy(OPPh)(HO)}{PWO}]·PhPO·HO () with pentagonal bipyramidal local coordination geometry. Magnetic measurements indicate that displays field-induced single-molecule magnet (SMM) behavior and the relaxation is dominated by under-barrier processes. exhibits spin-lattice relaxation at a broader temperature region with a reversal barrier over 300 K. Magneto-structural analysis reveals that the enhancement of SMM behavior originated from the equatorial replacement of PhPO by POM, which strengthens the axial anisotropy in . Luminescent experiments indicate that the characteristic Dy emissions of are covered up by the strong π-π* emission of PhPO at low-temperature regions. As for , partial Dy emission persists thanks to the antenna effect between Dy and POM.

摘要

具有各种配位方式的多金属氧酸盐(POMs)是构建单离子磁体(SIMs)的通用配体,但合成具有特定几何结构的POM-SIMs仍然是一个挑战。在此,我们合成了一种具有五角双锥局部配位几何结构的POM共结晶Dy-SIM [Dy(OPPh)(HO)][PWO]·4EtOH()和一种POM连接的Dy-SIM [{Dy(OPPh)(HO)}{PWO}]·PhPO·HO()。磁性测量表明,表现出场诱导单分子磁体(SMM)行为,且弛豫过程受势垒以下过程主导。在更宽的温度区域表现出自旋晶格弛豫,其反转势垒超过300 K。磁结构分析表明,SMM行为的增强源于POM对PhPO的赤道取代,这增强了中的轴向各向异性。发光实验表明,在低温区域,的特征Dy发射被PhPO的强π-π*发射掩盖。至于,由于Dy与POM之间的天线效应,部分Dy发射得以保留。

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