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多核锰家族的新成员:MnMn单分子磁体和MnMn反铁磁配合物。合成与磁结构相关性。

New members of the polynuclear manganese family: MnMn single-molecule magnets and MnMn antiferromagnetic complexes. Synthesis and magnetostructural correlations.

作者信息

Reis Conceição Nuno, Nesterova Oksana V, Rajnák Cyril, Boča Roman, Pombeiro Armando J L, Guedes da Silva M Fátima C, Nesterov Dmytro S

机构信息

Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal.

Department of Chemistry, Faculty of Natural Sciences, University of SS Cyril and Methodius, 917 01 Trnava, Slovakia.

出版信息

Dalton Trans. 2020 Oct 20;49(40):13970-13985. doi: 10.1039/d0dt02652b.

Abstract

The synthesis, crystal structures and magnetic properties are reported for three novel mixed-valence tetranuclear [MnII2MnIII2(HBuDea)2(BuDea)2(EBA)4] (1), [MnII2MnIII2(HBuDea)2(BuDea)2(DMBA)4] (2) and undecanuclear [MnII3MnIII8O4(OH)2(BuDea)6(DMBA)8] (3) clusters, where H2BuDea is N-butyldiethanolamine, HEBA is 2-ethylbutyric acid and HDMBA is 2,2-dimethylbutyric acid. The compounds have been prepared through self-assembly reactions of manganese(ii) chloride with H2BuDea and respective carboxylic acid in methanol solution in air, affording 1 with HEBA, and 2 or 3 with HDMBA, depending on the experimental conditions. The single crystal X-ray analysis reveals that 1 and 2 have similar centrosymmetric structures based on the {M4(μ3-O)2(μ-O)4} core, while 3 discloses the unprecedented {M11(μ-O)4(μ3-O)12} one. The Mn4 complexes display single-molecule magnet (SMM) behavior with a S = 9 spin ground state and a high energy barrier Ueff/kB of up to 51 K. The magnetic properties of 2 are successfully modeled with JMnIII-MnIII/hc = 25.7 cm-1 and two JMnIII-MnII/hc constants of 3.1 and -0.93 cm-1 (data correspond to the Ĥ = -Jŝ1·ŝ2 formalism). The Mn11 cluster exhibits a paramagnetic behavior with dominant antiferromagnetic coupling. A possible influence of intermolecular effects and of different peripheries of the magnetic cores designed by using 2-ethylbutyrate (in 1) or 2,2-dimethylbutyrate (in 2) on the magnetic properties of 1 and 2 is discussed. The experimental magnetostructural correlations for the {MnII2MnIII2(μ3-O)2(μ-O)4} cores, supported by broken symmetry DFT calculations, disclose the X-MnIIIMnIII angle and MnIII-O distance (where MnIII-X and MnIII-O are axial Jahn-Teller bonds) as the structural factors having the strongest influence on JMnIII-MnIII exchange coupling. It is shown that two JMnIII-MnII constants are necessary for the correct description of magnetic exchange couplings in the {MnII2MnIII2(μ3-O)2(μ-O)4} tetranuclear unit.

摘要

报道了三种新型混合价态四核[MnII2MnIII2(HBuDea)2(BuDea)2(EBA)4](1)、[MnII2MnIII2(HBuDea)2(BuDea)2(DMBA)4](2)和十一核[MnII3MnIII8O4(OH)2(BuDea)6(DMBA)8](3)簇合物的合成、晶体结构及磁性质,其中H2BuDea为N - 丁基二乙醇胺,HEBA为2 - 乙基丁酸,HDMBA为2,2 - 二甲基丁酸。这些化合物是通过氯化锰与H2BuDea及相应羧酸在空气中的甲醇溶液中进行自组装反应制备得到的,根据实验条件,得到含HEBA的1,以及含HDMBA的2或3。单晶X射线分析表明,1和2基于{M4(μ3 - O)2(μ - O)4}核具有相似的中心对称结构,而3展现出前所未有的{M11(μ - O)4(μ3 - O)12}结构。Mn4配合物表现出单分子磁体(SMM)行为,自旋基态S = 9,有效能垒Ueff/kB高达51 K。2的磁性质通过JMnIII - MnIII/hc = 25.7 cm-1以及两个JMnIII - MnII/hc常数3.1和 - 0.93 cm-1成功建模(数据对应于Ĥ = -Jŝ1·ŝ2形式)。Mn11簇表现出顺磁行为,主要为反铁磁耦合。讨论了分子间效应以及使用2 - 乙基丁酸盐(在1中)或2,2 - 二甲基丁酸盐(在2中)设计的磁核不同外围对1和2磁性质的可能影响。由破缺对称性DFT计算支持的{MII2MnIII2(μ3 - O)2(μ - O)4}核的实验磁结构相关性揭示,X - MnIIIMnIII角和MnIII - O距离(其中MnIII - X和MnIII - O为轴向 Jahn - Teller键)是对JMnIII - MnIII交换耦合影响最强的结构因素。结果表明,对于正确描述{MnII2MnIII2(μ3 - O)2(μ - O)4}四核单元中的磁交换耦合,需要两个JMnIII - MnII常数。

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