Semiquantitative studies on the correlations between the electrostatic potential of a single DyIII ion and its energy barrier in the containing-DyIII single molecule magnets†

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2025-02-13 DOI:10.1039/D5DT00017C
Jia-Rong Jiang, Yu-Jie Zhu, Wei-Nan Li, Yang Zhou and Hui-Sheng Wang
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Abstract

Although the design of containing-DyIII single molecule magnets (SMMs) based on electrostatic potential has been employed for several years, rational studies on the correlations between the electrostatic potential of a single DyIII ion and its energy barriers have not been reported previously. In this work, a novel “Y”-shaped MnIII5DyIII3 complex, [MnIII5DyIII3(NO3)(OCH3)(L)4(L′)2(tea)(teaH)4]OH·3CH3OH·2H2O (1, H2L = 2-methoxy-6-[(Z)-(1H-1,2,4-triazol-3-ylimino)methyl]phenol, H3tea = triethanolamine and HL′ = 2-hydroxy-3-methoxybenzaldehyde), was obtained through the reaction of the H2L ligand, teaH3, Dy(NO3)3·6H2O and MnCl2·4H2O in CH3OH and DMF. Structural analysis revealed that the coordination geometry of Dy1 in 1 is muffin-like (MFF-9, Cs), while the geometries of Dy2 and Dy3 fall among spherical capped square antiprism-like (CSAPR-9, C4v), spherical tricapped trigonal prism-like (TCTPR-9, D3h) and muffin-like (MFF-9, Cs). Magnetic studies indicated that 1 exhibits slow magnetic relaxation behavior under zero dc field. More importantly, for the first time, we proposed the two parameters Req and Rax to describe the relationship. The two parameters were employed for three DyIII ions in 1, one Zn2Dy complex and one mononuclear Dy complex reported by others. Results indicate that the calculated energy barrier (Ucal) continuously increases with decreasing Rax absolute values. However, the higher the Rax absolute values, the lower the Ucal values. This indicates that when the electrostatic potentials from two sides of the equatorial plane of DyIII are completely equivalent to each other, Ucal is the highest. Moreover, POLY_ANISO and DFT calculations for 1 indicated that except for J4 showing ferromagnetic coupling, all magnetic couplings are antiferromagnetic, which were interpreted from magneto-structural correlation.

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含Dy单分子磁体中DyIII离子静电势与能垒关系的半定量研究
基于静电势设计含Dy(III)单分子磁体(SMMs)已有多年历史,但对DyIII单离子静电势与其能垒之间关系的合理研究尚未见报道。本文通过H2L配体teaH3、Dy(NO3)3·6H2O和MnCl2·4H2O在CH3OH和DMF中反应,得到了一种新型的“Y”形MnIII5DyIII3配合物[MnIII5DyIII3(NO3)(OCH3)(L)4(L’)2(tea)(teaH)4]OH·3CH3OH·2H2O (1,h2l = 2-甲氧基-6-[(Z)-(1h -1,2,4-三唑-3-乙氧基)甲基]苯酚,H3tea =三乙醇胺,HL’= 2-羟基-3-甲氧基苯甲醛)。结构分析表明,Dy1 in 1的配位几何为松饼(MFF-9, Cs),而Dy2和Dy3的配位几何位于球顶方形反棱镜(capr -9, C4v)、球三向三角棱镜(TCTPR-9, D3h)和松饼(MFF-9, Cs)之间。磁性研究表明,1在零直流磁场下表现出缓慢的磁弛豫行为。更重要的是,我们首先提出了两个参数Req和Rax来描述这种关系。这两个参数用于1中的三个DyIII,一个Zn2Dy配合物以及其他报道的一个单核Dy配合物。结果表明,随着Rax绝对值的减小,计算得到的能垒(Ucal)不断增大。然而,Rax绝对值较大,Ucal较小。这表明当DyIII的赤道面两侧的静电电位完全相等时,其Ucal最大。此外,对1的POLY_ANISO和DFT计算表明,除了J4表现出铁磁耦合外,所有的磁耦合都是反铁磁的,这可以用磁结构相关来解释。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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