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基于硫代吡唑啉酮配体构建SCO活性二价铁单核配合物。

Construction of SCO-Active Fe(II) Mononuclear Complexes from the Thio-pybox Ligand.

作者信息

Pan Yao, Meng Yin-Shan, Liu Qiang, Gao Wan-Qing, Liu Chun-Hua, Liu Tao, Zhu Yuan-Yuan

机构信息

School of Chemistry and Chemical Engineering, Hefei University of Technology and Anhui Key Laboratory of Advanced Catalytic Materials and Reaction Engineering, Hefei 230009, China.

State Key Laboratory of Fine Chemicals, Dalian University of Technology, 2 Linggong Road, Dalian 116024, China.

出版信息

Inorg Chem. 2020 Jun 1;59(11):7398-7407. doi: 10.1021/acs.inorgchem.9b03506. Epub 2020 May 13.

Abstract

The development of new spin-crossover complexes provides novel promising switching materials with significant potential at the molecular level. Ter-imine-type molecules represent one of the important classes of ligands in creating SCO-active complexes. Herein we report a family of mononuclear Fe(II) SCO-active compounds constructed from a new type of ter-imine ligand named the thio-pybox ligand (2,6-bis(4,4-dimethyl-4,5-dihydrothiazol-2-yl)pyridine, ). Through the variation of counteranions, some cases display complete SCO and with near ambient temperature. Among them, annealed Fe(L) [] shows and as 319 and 349 K, respectively. The wide thermal hysteresis of Δ = 30 K originated from the weak interaction between complex cations and counteranions in the crystal lattice. Impressively, its high-spin population can be increased considerably by annealing at high temperature. The metastable high-spin phase is stable in the successive magnetic measurements and would gradually relax to its initial state with high population of low-spin configuration at ambient temperature. In acetonitrile-diluted solution, still maintains SCO with an estimated at 240 K. Differential scanning calorimetry discloses the structural phase at around 355 K in the first heating process and the increase in the high-spin population concomitant with annealing was also corroborated by Fe Mössbauer measurements. Additionally, the influences on SCO by counteranion and ligand structure are investigated, which show that the fine tuning of complex structures can affect the behavior of the spin state significantly. Finally, magneto-structural correlation studies were performed on the structures of and its oxygen analogue at multiple temperatures. The analyses of some structural parameters, including terminal N···N donor separation, bite angle, patulous angle, and the root mean squared deviation indicate that the replacement of the oxygen atom with a sulfur atom can effectively improve the flexibility and release the steric strain and thus tune the SCO toward ambient temperature. Our research demonstrates the rational design of the ligand can lead to new SCO-active compounds with high performance.

摘要

新型自旋交叉配合物的开发提供了在分子水平上具有巨大潜力的新型有前景的开关材料。三联吡啶型分子是创建自旋交叉活性配合物的重要配体类别之一。在此,我们报道了一系列由一种名为硫代吡唑啉酮配体(2,6-双(4,4-二甲基-4,5-二氢噻唑-2-基)吡啶)的新型三联吡啶配体构建的单核铁(II)自旋交叉活性化合物。通过抗衡阴离子的变化,一些情况显示出完全的自旋交叉,且转变温度接近室温。其中,退火后的Fe(L)₂在319 K和349 K分别显示出高低自旋态。ΔT = 30 K的宽热滞回源于晶格中配合物阳离子与抗衡阴离子之间的弱相互作用。令人印象深刻的是,通过高温退火,其高自旋态的占有率可以显著增加。亚稳态的高自旋相在连续的磁性测量中是稳定的,并且在室温下会逐渐弛豫到其初始的低自旋态高占有率状态。在乙腈稀释溶液中,Fe(L)₂在240 K时仍保持自旋交叉,估计转变温度为240 K。差示扫描量热法揭示了在第一次加热过程中约355 K处的结构相变,并且铁穆斯堡尔谱测量也证实了随着退火高自旋态占有率的增加。此外,研究了抗衡阴离子和配体结构对自旋交叉的影响,结果表明配合物结构的微调可以显著影响自旋态的行为。最后,在多个温度下对Fe(L)₂及其氧类似物的结构进行了磁结构相关性研究。对一些结构参数的分析,包括末端N···N供体间距、咬角、张开角和均方根偏差表明,用硫原子取代氧原子可以有效地提高灵活性并释放空间应变,从而将自旋交叉调节至室温附近。我们的研究表明,配体的合理设计可以导致具有高性能的新型自旋交叉活性化合物。

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