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Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41

机译:水对嵌入MCM-41孔中的Fe(II)1,2,4-三唑一维链自旋转变行为的影响

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摘要

The spin-crossover (SCO) compounds [Fe(Htrz)](BF)·HO (SCO-1) and [Fe(Htrz)trz]BF (SCO-2) (Htrz = 1,2,4-triazole) were embedded in the pores of mesostructured silica MCM-41 to yield SCO@MCM composites as evidenced by electron microscopy, gas sorption studies, powder X-ray diffractometry, atomic absorption and infrared spectrometry. Studies of the temperature-induced spin crossover behavior of the composites by temperature-variable Fe Mössbauer spectroscopy, magnetic and differential scanning calorimetry measurements and optical reflectivity indicate that the spin transition of the composites was significantly shifted for SCO-1@MCM to higher temperature in comparison to bulk SCO-1 compounds while the shift for SCO-2 was negligible. These shifts in the transition temperature for SCO-1@MCM [ bulk SCO-1] amounted to = 371/376 K [282/291 K] and = 340/345 K [276/286 K] (magnetic/optical reflectivity data) with a broadening of the hysteresis by 25–26 K relative to bulk SCO-1 (varying slightly with the used method). The significant difference in the SCO behavior of the similar materials SCO-1 and SCO-2 when embedded in the MCM-41 matrix is assigned to the hydration of the SCO-1@MCM material. Water is apparently crucial in transmitting the confinement pressure or matrix effect on the spin transition when the SCO compound is embedded between the pore walls.
机译:自旋交联(SCO)化合物[Fe(Htrz)](BF)·HO(SCO-1)和[Fe(Htrz)trz] BF(SCO-2)(Htrz = 1,2,4-三唑)为电子显微镜,气体吸收研究,粉末X射线衍射法,原子吸收法和红外光谱法证明,将其嵌入介孔结构的二氧化硅MCM-41的孔中可生成SCO @ MCM复合材料。通过温度可变的FeMössbauer光谱,磁和差示扫描量热法测量以及光反射率对复合物的温度诱导的自旋交叉行为的研究表明,对于SCO-1 @ MCM,复合物的自旋转变显着转移到更高的温度下。与散装SCO-1化合物相比,SCO-2的变化可忽略不计。 SCO-1 @ MCM [本体SCO-1]的转变温度的这些变化总计= 371/376 K [282/291 K]和= 340/345 K [276/286 K](磁/光反射率数据)相对于整体SCO-1,磁滞范围扩大了25–26 K(使用的方法略有变化)。当嵌入MCM-41基质中时,相似材料SCO-1和SCO-2的SCO行为的显着差异归因于SCO-1 @ MCM材料的水合作用。当SCO化合物嵌入孔壁之间时,水显然对传递自旋转变的约束压力或基体效应至关重要。

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