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镍钳形配合物中硝基苄基悬垂臂的电化学驱动摆动

Electrochemically Driven Swinging of a Nitrobenzyl Pendant Arm in a Nickel Scorpionand Complex.

作者信息

Ciarrocchi Carlo, Fabbrizzi Luigi, Licchelli Maurizio, Taglietti Angelo

机构信息

Dipartimento di Chimica, Università di Pavia, 27100, Pavia, Italy.

出版信息

Chemistry. 2022 May 6;28(26):e202200462. doi: 10.1002/chem.202200462. Epub 2022 Mar 29.

Abstract

A radical anion -NO is formed upon an electrochemically reversible one-electron reduction of the square-planar Ni complex of N-nitrobenzylcyclam. The -NO group goes to occupy an axial position of the metal ion, thus establishing a significant electronic interaction with the metal center. In particular, the ESR spectrum supports the occurrence of an electron transfer from -NO to the metal, which therefore presents a significant Ni character. On re-oxidation, the nitrobenzyl side chain detaches and the Ni complex is restored, providing an example of a fully reversible redox driven intramolecular motion.

摘要

N-硝基苄基环胺的平面正方形镍配合物发生电化学可逆的单电子还原反应时,会形成一种自由基阴离子-NO 。-NO 基团占据金属离子的轴向位置,从而与金属中心建立起显著的电子相互作用。特别是,电子顺磁共振光谱支持了从-NO 到金属的电子转移的发生,因此该金属呈现出显著的镍特性。再氧化时,硝基苄基侧链脱离,镍配合物得以恢复,这提供了一个完全可逆的氧化还原驱动的分子内运动的例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af90/9311437/81a356d6fc80/CHEM-28-0-g005.jpg

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