Iron(ii) complexes of 2,6-di(1H-pyrazol-3-yl)-pyridine derivatives with hydrogen bonding and sterically bulky substituents
作者:Thomas D. Roberts、Marc A. Little、Laurence J. Kershaw Cook、Malcolm A. Halcrow
DOI:10.1039/c4dt00355a
日期:——
Syntheses of 2,6-di(5-aminopyrazol-3-yl)pyridine (L1), 2,6-di(5-tertbutylcarboxamidopyrazol-3-yl)pyridine (L2), 2,6-di(5-tertbutylpyrazol-3-yl)pyridine (L3), 2-(5-tertbutylpyrazol-3-yl)-6-(5-methylpyrazol-3-yl)pyridine (L4) and 2-(5-tertbutylpyrazol-3-yl)-6-(5-aminopyrazol-3-yl)pyridine (L5) are reported. Iron complex salts of the first four ligands were crystallographically characterised. The structures exhibit intermolecular hydrogen bonding between the cations and the anions and/or solvent, leading to a fluorite (flu) net, a 1D ladder structure, and a homochiral self-penetrating helical network related to the (10,3)-a (srs) topology. All the complexes are high-spin in the crystal, and bulk samples are also fully or predominantly high-spin at room temperature and below although two of the dried materials exhibit partial spin-state transitions on cooling.
合成 2,6-二(5-氨基吡唑-3-基)吡啶 (L1)、2,6-二(5-叔丁基脒基吡唑-3-基)吡啶 (L2)、2,6-二(5-叔丁基吡唑-3-基)吡啶 (L3)、报告了 2-(5-叔丁基吡唑-3-基)-6-(5-甲基吡唑-3-基)吡啶 (L4) 和 2-(5-叔丁基吡唑-3-基)-6-(5-氨基吡唑-3-基)吡啶 (L5)。对前四种配体的铁络合盐进行了晶体学表征。这些结构显示了阳离子与阴离子和/或溶剂之间的分子间氢键,从而形成了萤石网(flu)、一维梯形结构以及与 (10,3)-a (srs) 拓扑相关的同手性自穿透螺旋网络。所有复合物在晶体中都是高自旋的,而块状样品在室温及以下也完全或主要是高自旋的,尽管其中两种干燥材料在冷却时会出现部分自旋态转变。