Kershaw Cook Laurence J, Fisher Julie, Harding Lindsay P, Halcrow Malcolm A
School of Chemistry, University of Leeds, Woodhouse Lane, Leeds, UK LS2 9JT.
Dalton Trans. 2015 May 28;44(20):9417-25. doi: 10.1039/c5dt00732a.
The syntheses of 4-mercapto-2,6-di(pyrazol-1-yl)pyridine (bppSH) and bis[2,6-di(pyrazol-1-yl)pyrid-4-yl]disulfide (bppSSbpp) are reported. In contrast to previously published "back-to-back" bis-[2,6-di(pyrazol-1-yl)pyridine] derivatives, which form coordination polymers with transition ions that are usually insoluble, bppSSbpp yields soluble oligomeric complexes with iron(ii) and zinc(ii). Mass spectrometry and DOSY data show that {Fe(μ-bppSSbpp)}n and {Zn(μ-bppSSbpp)}n form tetranuclear metallacycles in nitromethane solution (n = 4), although (1)H NMR and conductivity measurements imply the iron compound may undergo more fragmentation than its zinc congener. Both {Fe(bppSH)2 and {Fe(μ-bppSSbpp)}n exhibit thermal spin-crossover in CD3NO2 solution, with midpoint temperatures near 245 K. The similarity of these equilibria implies there is little cooperativity between the iron centres in the metallacyclic structures.
报道了4-巯基-2,6-二(吡唑-1-基)吡啶(bppSH)和双[2,6-二(吡唑-1-基)吡啶-4-基]二硫化物(bppSSbpp)的合成。与先前发表的“背对背”双[2,6-二(吡唑-1-基)吡啶]衍生物不同,后者与通常不溶的过渡离子形成配位聚合物,bppSSbpp与铁(II)和锌(II)形成可溶性低聚配合物。质谱和DOSY数据表明,{Fe(μ-bppSSbpp)}n和{Zn(μ-bppSSbpp)}n在硝基甲烷溶液中形成四核金属环(n = 4),尽管1H NMR和电导率测量表明铁化合物可能比其锌同类物经历更多的碎片化。{Fe(bppSH)2和{Fe(μ-bppSSbpp)}n在CD3NO2溶液中均表现出热自旋交叉,中点温度接近245 K。这些平衡的相似性意味着金属环结构中铁中心之间几乎没有协同作用。