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新型二维 Fe(II) 金属有机骨架{Fe(4-PhPy)(2)[M(II)(CN)(x)](y)}·sH(2)O 的热诱导和光诱导自旋交叉:光谱、结构和磁性研究。

Thermal- and light-induced spin crossover in novel 2D Fe(II) metalorganic frameworks {Fe(4-PhPy)(2)[M(II)(CN)(x)](y)}.sH(2)O: spectroscopic, structural, and magnetic studies.

机构信息

Institut für Anorganische und Analytische Chemie, Johannes-Gutenberg-Universität, Staudinger-Weg 9, D-55099 Mainz, Germany.

出版信息

Inorg Chem. 2009 Jul 6;48(13):6130-41. doi: 10.1021/ic900491r.

DOI:10.1021/ic900491r
PMID:19462941
Abstract

Five novel two-dimensional coordination polymers {Fe(4PhPy)(2)[M(II)(CN)(4)]}.sH(2)O (4PhyPy = 4-phenylpyridine; 1: M(II) = Pd, s = 0; 2: M(II) = Ni, s = 0; 3: M(II) = Pt, s = 1) and {Fe(4PhPy)(2)M(I)(CN)(2)}.sH(2)O (4: M(I) = Ag, s = 1; 5: M(I) = Au, s = 0.5) exhibiting spin-crossover properties have been synthesized. They were characterized at various temperatures using X-ray absorption spectroscopy (XAS), powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), and magnetic susceptibility measurements. The occurrence of a cooperative thermal spin transition detected by the magnetic method is located at critical temperatures T(c)( downward arrow)/T(c)( upward arrow) = 163 K/203 K (1), 135 K/158 K (2), and 172 K/221 K (3), and a less cooperative one is located at T(c) = 188 K (4) and 225 K (5). Compounds 1-5 show an abrupt color change from yellow (high-spin (HS) state) to red (low-spin (LS) state) upon spin-state conversion. The dehydration of the compounds changes the type of the spin transition, making it more abrupt and shifting the critical temperature to higher temperatures. For 1 and 2, XAS provides local structural information on the contraction of the FeN(6) coordination sphere upon the HS-to-LS transition, in line with the magnetic results. Variable-temperature characterization of 1 by X-ray diffraction evidences the very abrupt phase transition with a large hysteresis. A light-induced spin conversion (LIESST effect) is detected by magnetic measurements in 1-5 below 70 K.

摘要

五种新型二维配位聚合物{Fe(4PhPy)(2)[M(II)(CN)(4)]}.sH(2)O(4PhyPy=4-苯基吡啶;1:M(II)=Pd,s=0;2:M(II)=Ni,s=0;3:M(II)=Pt,s=1)和{Fe(4PhPy)(2)M(I)(CN)(2)}.sH(2)O(4:M(I)=Ag,s=1;5:M(I)=Au,s=0.5)具有自旋交叉性质,已被合成。它们在不同温度下通过 X 射线吸收光谱(XAS)、粉末 X 射线衍射(PXRD)、差示扫描量热法(DSC)和磁化率测量进行了表征。通过磁性方法检测到的协同热自旋转变发生在临界温度 T(c)(↓)/T(c)(↑)=163 K/203 K(1)、135 K/158 K(2)和 172 K/221 K(3),以及一个不那么协同的温度为 T(c)=188 K(4)和 225 K(5)。化合物 1-5 在自旋态转换时表现出从黄色(高自旋(HS)态)到红色(低自旋(LS)态)的急剧颜色变化。化合物的脱水改变了自旋转变的类型,使其变得更加急剧,并将临界温度升高到更高的温度。对于 1 和 2,XAS 提供了 HS 到 LS 转变时 FeN(6)配位球收缩的局部结构信息,与磁性结果一致。1 通过 X 射线衍射的变温特性证明了具有大滞后的非常急剧的相变。在 1-5 中,低于 70 K 的磁测量检测到光诱导自旋转换(LIESST 效应)。

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