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扭曲的分子磁体。

Twisted molecular magnets.

机构信息

EaStChem School of Chemistry, The University of Edinburgh, The Kings Buildings, West Mains Road, Edinburgh, EH9 3JJ, UK.

出版信息

Chem Commun (Camb). 2012 Jan 7;48(2):181-90. doi: 10.1039/c1cc13558a. Epub 2011 Sep 5.

Abstract

The use of derivatised salicylaldoximes in manganese chemistry has led to the synthesis of a family of approximately fifty hexanuclear ([Mn(III)(6)]) and thirty trinuclear ([Mn(III)(3)]) Single-Molecule Magnets (SMMs). Deliberate, targeted structural distortion of the metallic core afforded family members with increasingly puckered configurations, leading to a switch in the pairwise magnetic exchange from antiferromagnetic to ferromagnetic. Examination of both the structural and magnetic data revealed a semi-quantitative magneto-structural correlation, from which the factors governing the magnetic properties could be extracted and used for predicting the properties of new family members and even more complicated structures containing analogous building blocks. Herein we describe an overview of this extensive body of work and discuss its potential impact on similar systems.

摘要

在锰化学中使用衍生水杨醛肟导致了大约五十个六核([Mn(III)(6)])和三十个三核([Mn(III)(3)])单分子磁体(SMM)的合成。通过故意、有针对性地扭曲金属核心的结构,获得了具有越来越褶皱构型的成员,从而导致成对磁交换从反铁磁转变为铁磁。对结构和磁性数据的检查揭示了半定量的磁结构相关性,从中可以提取出控制磁性性质的因素,并用于预测新成员的性质,甚至更复杂的结构包含类似的构建块。本文概述了这一广泛工作,并讨论了其对类似系统的潜在影响。

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