羧酸配体取代基对席夫碱型双核镝(Ⅲ)配合物结构和磁性的影响
Replacement of Carboxylate Ligand Substituent on Modulation of Structures and Magnetic Properties in Salen-Type Dinuclear Dy(Ⅲ) Complexes
作者单位E-mail
李敏 晋中学院化学化工系, 晋中 030619  
武海鹏 晋中学院化学化工系, 晋中 030619 wuhp@jzxy.edu.cn 
张盛 宝鸡文理学院化学化工学院, 宝鸡 721013  
刘毓芳 晋中学院化学化工系, 晋中 030619  
陈勇强 晋中学院化学化工系, 晋中 030619 chenyongqiang@jzxy.edu.cn 
陈三平 西北大学化学与材料科学学院, 西安 710127 sanpingchen@126.com 
摘要: N-(2-羟基-3-甲氧基亚苄基)氨基脲(H2hms)与不同取代基的羧酸(RCOOH)为配体,合成了3例席夫碱类的中心对称双核镝基配合物[Dy2(Hhms)2(C(CH33COO)2(H2O)4](NO321)、[Dy2(Hhms)2(C14H9COO)2(C2H5OH)2(CH3OH)2][ZnCl4](2)和[Dy2(Hhms)2(C6H3(NH22COO)2Cl2]·2CH3CN(3),并对其进行了结构和磁性表征。结构分析表明,配合物12保持了相似的单帽四方反棱柱配位构型,但12中羧酸与Dy(Ⅲ)键合的方式不同;配合物23保持了相似的酚氧和羧酸桥联结构,但由于配位小分子的不同,配合物3中Dy(Ⅲ)离子的配位几何构型与2有所不同。磁性测试结果表明,配合物3在零场下观察到显著的单分子磁体行为,具有磁翻转有效能垒96 K。相反,配合物1仅表现了快的量子隧穿弛豫行为,甚至配合物2没有单分子磁体的弛豫信号。借助结构特点和各向异性轴取向等关键信息,对3例配合物的磁构效关系进行了讨论。研究结果表明利用羧酸配体取代基能够实现对分子磁各向异性以及对称性的良好调控,从而提高镧系单分子磁体磁弛豫行为。
关键词: 双核化合物    磁性  羧酸配体  单分子磁体
基金项目: 山西省“1331工程”重点创新团队(培育)建设计划(No.py201817)、山西省基础研究计划(自由探索类)项目(No.20210302124461)、山西省高等学校科技创新项目(No.2021L496、2021L497)和晋中学院博士科研经费资助。
Abstract: Three salen - type centrosymmetric dinuclear Dy (Ⅲ) complexes, [Dy2(Hhms)2(C(CH3)3COO)2(H2O)4](NO3)2 (1), [Dy2(Hhms)2(C14H9COO)2(C2H5OH)2(CH3OH)2][ZnCl4] (2), and [Dy2(Hhms)2(C6H3(NH2)2COO)2Cl2]·2CH3CN (3) (H2hms=(2-hydroxy-3-methoxybenzylidene)-semicarbazide), were isolated with different substituted carboxylic acid ligand, and were characterized structurally and magnetically. Structural analyses illustrate that the Dy (Ⅲ) ions in complexes 1 and 2 maintain similar monocapped square-antiprism geometries, but the coordination mode of carboxylate in 1 is different from that in 2; complexes 2 and 3 possess similar phenoxy oxygen and carboxylate bridged structure whereas the coordination geometries around the Dy(Ⅲ) ions are different between 3 and 2 due to the difference of coordinated small molecules. Magnetic characterizations reveal that significant single - molecule magnet (SMM) behavior was observed under zero dc field for complex 3, with an effective energy barrier to the reversal of magnetization of 96 K. Conversely, complex 1 only showed fast quantum tunneling relaxation even 2 was SMM-silent. Furthermore, the magneto-structural correlations in these Dy2 complexes were discussed. The results indicate that utility of carboxylate ligand substituent can give rise to good modulation in the molecular anisotropy and symmetry, hence the enhanced magnetic relaxation.
Keywords: dinuclear complex  dysprosium  magnetic properties  carboxylate ligand  single-molecule magnets
投稿时间:2021-08-08 修订日期:2021-10-31
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李敏,武海鹏,张盛,刘毓芳,陈勇强,陈三平.羧酸配体取代基对席夫碱型双核镝(Ⅲ)配合物结构和磁性的影响[J].无机化学学报,2022,38(1):171-180.
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Support information: 相关附件:   file210376_Supporting_information.doc