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Divergent Coordination Chemistry: Parallel Synthesis of 2×2 Iron(II) Grid‐Complex Tauto‐Conformers

机译:发散配位化学:2×2铁(II)网格复杂的互变异构体的平行合成。

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摘要

The coordination of iron(II) ions by a homoditopic ligand >L with two tridentate chelates leads to the tautomerism‐driven emergence of complexity, with isomeric tetramers and trimers as the coordination products. The structures of the two dominant [FeII 4 >L 4]8+ complexes were determined by X‐ray diffraction, and the distinctness of the products was confirmed by ion‐mobility mass spectrometry. Moreover, these two isomers display contrasting magnetic properties (FeII spin crossover vs. a blocked FeII high‐spin state). These results demonstrate how the coordination of a metal ion to a ligand that can undergo tautomerization can increase, at a higher hierarchical level, complexity, here expressed by the formation of isomeric molecular assemblies with distinct physical properties. Such results are of importance for improving our understanding of the emergence of complexity in chemistry and biology.
机译:同位配体> L 与两个三齿螯合物对铁离子的配位导致互变异构驱动的复杂性的出现,同分异构的四聚体和三聚体作为配位产物。通过X射线衍射确定了两种主要的[Fe II 4 > L 4] 8 + 配合物的结构,产品通过离子迁移质谱法确认。此外,这两种异构体显示出相反的磁性(Fe II 自旋交叉与受阻的Fe II 高自旋态)。这些结果证明金属离子与可经历互变异构的配体的配位如何在更高的层次水平上增加复杂性,在此通过具有不同物理性质的异构分子组装体的表达来表示。这些结果对于增进我们对化学和生物学中复杂性出现的理解至关重要。

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