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基于混合羧酸盐配体的 Mn12 氧代羧酸簇的新型单分子磁体,[Mn12O12(CN-o-C6H4CO2)12(CH3CO2)4(H2O)4]·8CH2Cl2:合成、晶体和电子结构、磁性。

New single-molecule magnet based on Mn12 oxocarboxylate clusters with mixed carboxylate ligands, [Mn12O12(CN-o-C6H4CO2)12(CH3CO2)4(H2O)4]·8CH2Cl2: Synthesis, crystal and electronic structure, magnetic properties.

机构信息

Institute of Problems of Chemical Physics Russian Academy of Sciences, Semenov's av., 1, Chernogolovka 142432, MD, Russian Federation.

出版信息

Dalton Trans. 2012 Nov 28;41(44):13747-54. doi: 10.1039/c2dt31173a. Epub 2012 Oct 11.

DOI:10.1039/c2dt31173a
PMID:23059752
Abstract

A new high symmetry Mn(12) oxocarboxylate cluster [Mn(12)O(12)(CN-o-C(6)H(4)CO(2))(12)(CH(3)CO(2))(4)(H(2)O)(4)]·8CH(2)Cl(2) (1) with mixed carboxylate ligands is reported. It was synthesized by the standard carboxylate substitution method. 1 crystallizes in the tetragonal space group I4(1)/a. Complex 1 contains a [Mn(12)O(12)] core with eight CN-o-C(6)H(4)CO(2) ligands in the axial positions, four CH(3)CO(2) and four CN-o-C(6)H(4)CO(2) in equatorial positions. Four H(2)O molecules are bonded to four Mn atoms in an alternating up, down, up, down arrangement indicating a 1 : 1 : 1 : 1 isomer. The Mn(12) molecules in 1 are self-assembled by complementary hydrogen C-H···N bonds formed with participation of the axial o-cyanobenzoate ligands of the adjacent Mn(12) clusters. The lattice solvent molecules (CH(2)Cl(2)) are weakly interacted with Mn(12) units that results in solvent loss immediately after removal of the crystals from the mother liquor. The electronic structure and the intramolecular exchange parameters have been calculated. Mn 3d bands of 1 are rather broad, and the center of gravity of the bands shifts down from the Fermi level. The overlap between Mn 3d bands and 2p ones of the oxygen atoms from the carboxylate bridges is higher than in the parent Mn(12)-acetate cluster. These changes in the electronic structure provide a significant difference in the exchange interactions in comparison to Mn(12)-acetate. The magnetic properties have been studied on a dried (solvent-free) polycrystalline sample of 1. The dc magnetic susceptibility measurements in the 2-300 K temperature range support a high-spin ground state (S = 10). A bifurcation of temperature dependencies of magnetization taken under zero field cooled and field cooled conditions observed below 4.5 K is due to slow magnetization relaxation. Magnetization versus applied dc field exhibited a stepwise hysteresis loop at 2 K. The ac magnetic susceptibility data revealed the frequency dependent out-of-phase (χ(M)'') signals characteristic of single-molecule magnets.

摘要

一种具有混合羧酸盐配体的新型高对称 Mn(12) 氧代羧酸簇[Mn(12)O(12)(CN-o-C(6)H(4)CO(2))(12)(CH(3)CO(2))(4)(H(2)O)(4)]·8CH(2)Cl(2)(1)被报道。它是通过标准的羧酸盐取代法合成的。1 在四方晶系 I4(1)/a 中结晶。配合物 1 包含一个[Mn(12)O(12)]核心,在轴向位置有八个 CN-o-C(6)H(4)CO(2)配体,在赤道位置有四个 CH(3)CO(2)和四个 CN-o-C(6)H(4)CO(2)。四个 H(2)O 分子与四个 Mn 原子成键,呈交替的上下、上下排列,表明存在 1:1:1:1 的异构体。1 中的 Mn(12)分子通过相邻 Mn(12)簇的轴向 o-氰基苯甲酸配体参与形成的互补氢键自组装。晶格溶剂分子(CH(2)Cl(2))与 Mn(12)单元弱相互作用,导致晶体从母液中取出后立即失去溶剂。已经计算了电子结构和分子内交换参数。1 的 Mn 3d 带相当宽,带的重心从费米能级向下移动。Mn 3d 带与羧酸盐桥的氧原子的 2p 带之间的重叠高于母体 Mn(12)-乙酸盐簇。这些电子结构的变化与 Mn(12)-乙酸盐相比,在交换相互作用方面有显著的差异。已经在 1 的干燥(无溶剂)多晶样品上研究了磁性。在 2-300 K 的温度范围内进行的直流磁化率测量支持高自旋基态(S = 10)。在 4.5 K 以下观察到零场冷却和场冷却条件下磁化强度温度依赖性的分叉归因于缓慢的磁化弛豫。施加直流磁场时的磁化对表现出在 2 K 时的阶跃式滞后环。交流磁化率数据显示出与单分子磁体相关的频率相关的反相(χ(M)')信号。

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