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单链磁体的三维反铁磁有序:一种设计基于分子的磁体的新方法。

Three-dimensional antiferromagnetic order of single-chain magnets: a new approach to design molecule-based magnets.

机构信息

Department of Chemistry, Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza-Aoba, Aoba-ku, Sendai, Miyagi 980-8578, Japan.

出版信息

Chemistry. 2010 Mar 22;16(12):3656-62. doi: 10.1002/chem.200902861.

Abstract

Two one-dimensional compounds composed of a 1:1 ratio of Mn(III) salen-type complex and Ni(II) oximato moiety with different counter anions, PF(6)(-) and BPh(4)(-), were synthesized: [Mn(3,5-Cl(2)saltmen)Ni(pao)(2)(phen)]PF(6) (1) and [Mn(5-Clsaltmen)Ni(pao)(2)(phen)]BPh(4) (2), where 3,5-Cl(2)saltmen(2-) = N,N'-(1,1,2,2-tetramethylethylene)bis(3,5-dichlorosalicylideneiminate); 5-Clsaltmen(2-) = N,N'-(1,1,2,2-tetramethylethylene)bis(5-chlorosalicylideneiminate); pao(-) = pyridine-2-aldoximate; and phen = 1,10-phenanthroline. Single-crystal X-ray diffraction study was carried out for both compounds. In 1 and 2, the chain topology is very similar forming an alternating linear chain with a [-Mn(III)-ON-Ni(II)-NO-] repeating motif (where -ON- is the oximate bridge). The use of a bulky counteranion, such as BPh(4)(-), located between the chains in 2 rather than PF(6)(-) in 1, successfully led to the magnetic isolation of the chains in 2. This minimization of the interchain interactions allows the study of the intrinsic magnetic properties of the chains present in 1 and 2. While 1 and 2 possess, as expected, very similar paramagnetic properties above 15 K, their ground state is antiferromagnetic below 9.4 K and paramagnetic down to 1.8 K, respectively. Nevertheless, both compounds exhibit a magnet-type behavior at temperatures below 6 K. While for 2, the observed magnetism is well explained by a Single-Chain Magnet (SCM) behavior, the magnet properties for 1 are induced by the presence in the material of SCM building units that order antiferromagnetically. By controlling both intra- and interchain magnetic interactions in this new [Mn(III)Ni(II)] SCM system, a remarkable AF phase with a magnet-type behavior has been stabilized in relation with the intrinsic SCM properties of the chains present in 1. This result suggests that the simultaneous enhancement of both intrachain (J) and interchain (J') magnetic interactions (with keeping J >> J'), independently of the presence of AF phase might be an efficient route to design high temperature SCM-based magnets.

摘要

两种一维化合物由 Mn(III) salen 型配合物和 Ni(II) 氧肟酸盐部分以 1:1 的比例组成,具有不同的抗衡阴离子,PF(6)(-)和 BPh(4)(-):[Mn(3,5-Cl(2)saltmen)Ni(pao)(2)(phen)]PF(6) (1) 和 [Mn(5-Clsaltmen)Ni(pao)(2)(phen)]BPh(4) (2),其中 3,5-Cl(2)saltmen(2-) = N,N'-(1,1,2,2-四甲基亚乙基)双(3,5-二氯水杨醛亚胺);5-Clsaltmen(2-) = N,N'-(1,1,2,2-四甲基亚乙基)双(5-氯水杨醛亚胺);pao(-) = 吡啶-2-醛肟;和 phen = 1,10-菲咯啉。对这两种化合物进行了单晶 X 射线衍射研究。在 1 和 2 中,链拓扑结构非常相似,形成具有 [-Mn(III)-ON-Ni(II)-NO-] 重复基序的交替线性链(其中-ON- 是肟桥)。使用体积较大的抗衡阴离子,例如 BPh(4)(-),位于 2 中链之间,而不是 1 中的 PF(6)(-),成功地将 2 中的链磁隔离。这种减少链间相互作用的作用允许研究 1 和 2 中存在的链的固有磁性。虽然 1 和 2 在 15 K 以上具有非常相似的顺磁性质,但它们的基态在 9.4 K 以下为反铁磁,在 1.8 K 以下为顺磁,分别。然而,这两种化合物在低于 6 K 的温度下都表现出磁型行为。虽然对于 2,观察到的磁性可以很好地解释为单链磁体 (SCM) 行为,但对于 1,磁性质是由材料中存在反铁磁有序的 SCM 构建单元引起的。通过控制这个新的 [Mn(III)Ni(II)] SCM 系统中的内链和链间磁相互作用,可以稳定具有磁型行为的显著反铁磁相,与 1 中存在的链的固有 SCM 性质有关。这一结果表明,同时增强链内(J)和链间(J')磁相互作用(保持 J >> J'),而不考虑反铁磁相的存在,可能是设计高温 SCM 基磁体的有效途径。

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