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电刺激诱导的 Ni 中心配位诱导自旋态转变。

Ni-Centered Coordination-Induced Spin-State Switching Triggered by Electrical Stimulation.

机构信息

ENSL, CNRS, Laboratoire de Chimie UMR 5182, 46 allée d'Italie, 69342 Lyon, France.

Institut Universitaire de France, 5 rue Descartes, 75005 Paris, France.

出版信息

J Am Chem Soc. 2022 Oct 5;144(39):17955-17965. doi: 10.1021/jacs.2c07196. Epub 2022 Sep 26.

Abstract

We herein report the synthesis and magnetic properties of a Ni(II)-porphyrin tethered to an imidazole ligand through a flexible electron-responsive mechanical hinge. The latter is capable of undergoing a large amplitude and fully reversible folding motion under the effect of electrical stimulation. This redox-triggered movement is exploited to force the axial coordination of the appended imidazole ligand onto the square-planar Ni(II) center, resulting in a change in its spin state from low spin ( = 0) to high spin ( = 1) proceeding with an 80% switching efficiency. The driving force of this reversible folding motion is the π-dimerization between two electrogenerated viologen cation radicals. The folding motion and the associated spin state switching are demonstrated on the grounds of NMR, (spectro)electrochemical, and magnetic data supported by quantum calculations.

摘要

我们在此报告了一种通过柔性电子响应机械铰链将咪唑配体连接到镍(II)卟啉上的合成和磁性。后者能够在电刺激的作用下进行大振幅和完全可逆的折叠运动。这种氧化还原触发的运动被用来迫使附加的咪唑配体轴向配位到平面正方形的 Ni(II)中心,从而导致其自旋状态从低自旋( = 0)转变为高自旋( = 1),转换效率为 80%。这种可逆折叠运动的驱动力是两个电生成的二茂铁阳离子自由基之间的π-二聚化。折叠运动和相关的自旋状态转换是通过 NMR、(光谱)电化学和量子计算支持的磁性数据来证明的。

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