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含一至四个氮原子的氮杂苯超分子配合物的最新进展:合成策略、结构和磁性

Recent developments in supramolecular complexes of azabenzenes containing one to four N atoms: synthetic strategies, structures, and magnetic properties.

作者信息

Singh Juhi, Panda Suvam Kumar, Singh Akhilesh Kumar

机构信息

School of Basic Sciences, Indian Institute of Technology Bhubaneswar Bhubaneswar 752 050 India

出版信息

RSC Adv. 2022 Jun 29;12(29):18945-18972. doi: 10.1039/d2ra03455g. eCollection 2022 Jun 22.

DOI:10.1039/d2ra03455g
PMID:35873336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9240818/
Abstract

For the last couple of decades, azabenzene-based ligands have drawn much attention from inorganic chemists due to their ability to coordinate with different metal ions to form supramolecular clusters. These azabenzenes are weak σ donors and strong π acceptors and electron-deficient. Metallogrid complexes and non-grid oligomers are well-defined supramolecular clusters, formed by appropriate chelating ligands, and can show interesting optical, magnetic, and electronic properties. Self-assembly of [ × ] metallogrid complexes is dominated by the entropic factor while the formation of oligonuclear metal ion complexes is dominated by other effects like CFSE, electrostatic factors, ligand conformational characters, Herein, the present article gives an overview of six-membered heterocyclic azine-based ligands and their potential for different metal ions to form polynuclear complexes. Moreover, their temperature-dependent magnetic properties and SCO phenomena are well described and tabulated.

摘要

在过去的几十年里,基于氮杂苯的配体因其能够与不同金属离子配位形成超分子簇而备受无机化学家的关注。这些氮杂苯是弱σ供体、强π受体且缺电子。金属网格配合物和非网格低聚物是由合适的螯合配体形成的结构明确的超分子簇,并且可以表现出有趣的光学、磁性和电子性质。[×]金属网格配合物的自组装受熵因素主导,而多核金属离子配合物的形成则受其他效应如晶体场稳定化能(CFSE)、静电因素、配体构象特征等的主导。在此,本文概述了基于六元杂环氮嗪的配体及其与不同金属离子形成多核配合物的潜力。此外,还对它们的温度依赖性磁性质和自旋交叉(SCO)现象进行了详细描述并列表展示。

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