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具有铁磁相互作用的混合价七核铁配合物。

Mixed-valence heptanuclear iron complexes with ferromagnetic interaction.

机构信息

Institute of Inorganic Chemistry, Faculty of Chemical and Food Technology, Slovak University of Technology, SK-812 37 Bratislava, Slovakia.

出版信息

Inorg Chem. 2012 Dec 3;51(23):12755-67. doi: 10.1021/ic3015833. Epub 2012 Nov 12.

Abstract

Three new Prussian blue analogues, heptanuclear mixed-valence iron complexes of the type [Fe(II)(CN)(6){Fe(III)(1(-2H))}(6)]Cl(2)·nH(2)O, were synthesized and structurally and spectrally characterized, and their magnetic properties were investigated (1(-2H) corresponds to doubly deprotoned Schiff-base pentadentate ligands 1a, N,N'-bis(2-hydroxybenzylidene)-1,5-diamino-3-azapentane, 1b, N,N'-bis(3-ethoxy-2-hydroxybenzylidene)-1,7-diamino-4-azaheptane, or 1c, N,N'-bis(3-methoxy-2-hydroxybenzylidene)-1,6-diamino-3-azahexane). These compounds were formed by assembling the Fe(CN)(6) building block with mononuclear complexes of the [Fe(1(-2H))Cl] type. X-ray structure analysis revealed that the complexes adopt a star-like architecture: the Fe(II) ion lies at the very center, and on its octahedral nodes the Fe(III) sites are coordinated in the Fe(II)-C≡N-Fe(III) manner. The Schiff-base pentadentate ligand moiety 1(-2H) coordinates a single Fe(III) center in two complexes 3b and 3c. Ligands 1a(-2H) in the complex cation of 3a adopt an unusual coordination mode: three donor atoms of the same ligand (one O and two N) coordinate one Fe(III), whereas the remaining N' and O' donor atoms coordinate the neighboring Fe(III) center creating the {Fe(ON(2))(N'O')N″} chromophore involving two 1a(-2H) ligand moieties. Moreover, three Fe(III) centers are interconnected with three 1a(-2H) ligands in such a manner that two {Fe(III)(3)(1a(-2H))(3)} units form two intramolecular rings. Magnetic investigation of the heptanuclear complexes revealed the high-spin state of all six Fe(III) coordination sites (s = 5/2), while the very central Fe(II) site is in the low-spin state (s = 0). At low temperature, the ferromagnetic exchange interactions stay evident for all three complexes. Mössbauer spectra of compounds 3a and 3b revealed a presence of two different doublets for both compounds: the major doublet is related to six Fe(III) high-spin coordination sites and the minor doublet refers to the low-spin very central Fe(II).

摘要

三种新的普鲁士蓝类似物,即[Fe(II)(CN)6]{Fe(III)(1(-2H))}(6)]Cl2·nH2O 的七核混合价铁配合物,已被合成并进行了结构和光谱表征,其磁性性质也进行了研究(1(-2H) 对应于双去质子化的席夫碱五齿配体 1a、N,N'-双(2-羟基亚苄基)-1,5-二氨基-3-氮杂戊烷、1b、N,N'-双(3-乙氧基-2-羟基亚苄基)-1,7-二氨基-4-氮杂庚烷或 1c、N,N'-双(3-甲氧基-2-羟基亚苄基)-1,6-二氨基-3-氮杂己烷)。这些化合物是通过组装Fe(CN)6 结构单元与[Fe(1(-2H))Cl] 类型的单核配合物形成的。X 射线结构分析表明,这些配合物采用星形结构:Fe(II) 离子位于中心位置,其八面体节点配位有 Fe(III) 位点,以 Fe(II)-C≡N-Fe(III) 的方式配位。席夫碱五齿配体部分 1(-2H) 在 3b 和 3c 两个配合物中配位单个 Fe(III) 中心。配合物阳离子中的配体 1a(-2H) 在 3a 中采用一种不寻常的配位模式:同一配体的三个供体原子(一个 O 和两个 N)配位一个 Fe(III),而剩余的 N' 和 O' 供体原子配位相邻的 Fe(III) 中心,形成涉及两个 1a(-2H) 配体部分的{Fe(ON(2))(N'O')N″}发色团。此外,三个 Fe(III) 中心与三个 1a(-2H) 配体以这样的方式相互连接,即两个{Fe(III)(3)(1a(-2H))(3)}单元形成两个分子内环。对七核配合物的磁性研究表明,所有六个 Fe(III) 配位位点均处于高自旋态(s = 5/2),而非常中心的 Fe(II) 位点处于低自旋态(s = 0)。在低温下,所有三个配合物的铁磁交换相互作用仍然明显。化合物 3a 和 3b 的穆斯堡尔光谱显示,这两种化合物都存在两个不同的双峰:主要双峰与六个 Fe(III) 高自旋配位位点有关,而较小的双峰与低自旋的非常中心 Fe(II) 有关。

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