EastCHEM School of Chemistry, The University of Edinburgh, West Mains Road, Edinburgh, EH9 3 JJ, UK.
Chemistry. 2011 Jun 27;17(27):7521-30. doi: 10.1002/chem.201003327. Epub 2011 May 18.
In the cone conformation calix[4]arenes possess lower-rim polyphenolic pockets that are ideal for the complexation of various transition-metal centres. Reaction of these molecules with manganese salts in the presence of an appropriate base (and in some cases co-ligand) results in the formation of a family of calixarene-supported [Mn(III)(2)Mn(II)(2)] clusters that behave as single-molecule magnets (SMMs). Variation in the alkyl groups present at the upper-rim of the cone allows for the expression of a degree of control over the self-assembly of these SMM building blocks, whilst retaining the general magnetic properties. The presence of various different ligands around the periphery of the magnetic core has some effect over the extended self-assembly of these SMMs.
在锥形构象的杯[4]芳烃中,具有较低边缘的多酚口袋,非常适合各种过渡金属中心的络合。这些分子与锰盐在适当的碱(在某些情况下是共配体)存在下反应,导致杯芳烃支持的[Mn(III)(2)Mn(II)(2)]簇的形成,这些簇表现为单分子磁铁(SMM)。在锥形构象的上边缘存在的烷基基团的变化允许对这些 SMM 构建块的自组装进行一定程度的控制,同时保持一般的磁性性质。在磁性核的外围存在各种不同的配体对这些 SMM 的扩展自组装有一定的影响。