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光致激发自旋态捕获效应对[Fe(mepy)3tren](PF6)2 溶剂化晶体的影响。

Light-induced excited spin state trapping effect on [Fe(mepy)3tren](PF6)2 solvated crystals.

机构信息

Université Paris Sud, ICMMO-ECI, UMR CNRS 8182, Université Paris-Sud, 91405 Orsay, France.

出版信息

Dalton Trans. 2014 Jan 21;43(3):1063-71. doi: 10.1039/c3dt52495g. Epub 2013 Oct 28.

Abstract

A spin-crossover solvated compound Fe(mepy)3tren2·C7H8·C2H3N has been prepared and its switching properties have been compared to those reported for the non-solvated solid. The thermal spin transition occurs at 88 K with the opening of a 3.5 K wide hysteresis loop, while a fairly steep transition at 215 K without hysteresis has been previously reported for the non-solvated analogue. This feature has been rationalized by the analysis of the high-spin (HS) and low-spin (LS) structures, evidencing a relative stabilization of the high-spin state, as well as strong intermolecular interactions in the solvated compound. The photoswitching of the solvated solid, based on the light-induced excited spin state trapping effect, leads to a quantitative transformation from the low-spin to the high-spin state at 10 K. The long lifetime of the metastable HS state at 10 K allows the measurement of the photo-induced HS structure, where the cooperative interactions are enhanced, compared to those of the thermally populated HS structure. Then,the HS-to-LS relaxations have been studied between 45 and 60 K. They are sigmoidal in shape and can be well fitted in the frame of the mean-field approximation. The relative stability of the photo-induced HS state in this family of spin crossover compounds is not directly related to their thermal spin transition temperature. This unexpected observation is rationalized by a careful analysis of their structural characteristics.

摘要

已制备了一种自旋交叉溶剂化化合物Fe(mepy)3tren2·C7H8·C2H3N,并将其开关性能与非溶剂化固体报道的性能进行了比较。热自旋转变在 88 K 发生,具有 3.5 K 的宽滞后环,而先前报道的非溶剂化类似物在 215 K 时没有滞后发生相当陡峭的转变。通过对高自旋(HS)和低自旋(LS)结构的分析,这一特征得到了合理化,表明高自旋态的相对稳定,以及溶剂化化合物中强的分子间相互作用。基于光致激发自旋态俘获效应的溶剂化固体的光开关作用,导致在 10 K 时从低自旋态到高自旋态的定量转变。在 10 K 时,亚稳态 HS 态的长寿命允许测量光致 HS 结构,与热填充 HS 结构相比,协同相互作用得到增强。然后,在 45 到 60 K 之间研究了 HS 到 LS 的弛豫过程。它们呈 sigmoidal 形状,可以很好地用平均场近似拟合。在自旋交叉化合物的这个家族中,光致 HS 态的相对稳定性与它们的热自旋转变温度没有直接关系。这种意外观察结果通过对其结构特征的仔细分析得到了合理化。

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