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由于对称性破缺相变而呈现异常自旋交叉行为的[Au(CN)]-武装[FeFe]方形配合物

[Au(CN)]-Armed [FeFe] Square Complex Showing Unusual Spin-Crossover Behavior Due to a Symmetry-Breaking Phase Transition.

作者信息

You Maolin, Shao Dong, Deng Yi-Fei, Yang Jiong, Yao Nian-Tao, Meng Yin-Shan, Ungur Liviu, Zhang Yuan-Zhu

机构信息

Department of Chemistry, Southern University of Science and Technology (SUSTech), Shenzhen 518055, China.

Department of Chemistry, National University of Singapore, Science Drive 3, Singapore 117543.

出版信息

Inorg Chem. 2022 Apr 18;61(15):5855-5860. doi: 10.1021/acs.inorgchem.2c00192. Epub 2022 Apr 4.

Abstract

The incorporation of two different cyanide building blocks of [(Tp)Fe(CN)] and [Au(CN)] into one molecule afforded a novel hexanuclear [FeFeAu] complex (), in which the cyanide-bridged [FeFe] square was further grafted by two [Au(CN)] fragments as long arms in orientations. Complex undergoes a gradual spin crossover (SCO) ffrom low-spin (LS) to high-spin (HS) state for the Fe(II) centers upon desolvation. Remarkably, its desolvated phase () exhibits a reversible but atypical two-step (sharp-gradual) SCO behavior with considerable hysteresis (21 K). Variable-temperature single-crystal X-ray structural studies reveal that the hysteretic spin transition takes place synchronously with the concerted displacive motions of the molecules, representing another rare example including multistep and hysteretic spin transitions due to the synergetic SCO and structural phase transition.

摘要

将两种不同的氰化物构建单元[(Tp)Fe(CN)]和[Au(CN)]合并到一个分子中,得到了一种新型的六核[FeFeAu]配合物(),其中氰化物桥连的[FeFe]正方形通过两个[Au(CN)]片段作为长臂在特定取向上进一步接枝。配合物在去溶剂化时,Fe(II)中心经历从低自旋(LS)到高自旋(HS)状态的逐渐自旋交叉(SCO)。值得注意的是,其去溶剂化相()表现出可逆但非典型的两步(急剧 - 逐渐)SCO行为,具有相当大的滞后(21 K)。变温单晶X射线结构研究表明,滞后自旋转变与分子的协同位移运动同步发生,这代表了另一个罕见的例子,即由于协同SCO和结构相变导致的多步和滞后自旋转变。

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