Institut für Nanotechnologie, Karlsruher Institut für Technologie (KIT), Hermann-von-Helmholtz-Platz 1, 76344, Eggenstein-Leopoldshafen, Germany.
Fachbereich Physik, Technische Universität Kaiserslautern (TUK), Erwin-Schrödinger-Strasse 46, 67663, Kaiserslautern, Germany.
Angew Chem Int Ed Engl. 2016 Aug 26;55(36):10881-5. doi: 10.1002/anie.201603916. Epub 2016 Jul 13.
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 Fe(II) 4 L4 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 (Fe(II) spin crossover vs. a blocked Fe(II) 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.
由具有两个三角配位体的同双齿配体 L 协调铁(II)离子,导致复杂的互变异构驱动出现,其中异构体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)4L4 配合物的结构,并通过离子迁移质谱确认了产物的独特性。此外,这两种异构体表现出截然不同的磁性性质(Fe(II) 自旋交叉与受阻 Fe(II) 高自旋态)。这些结果表明,金属离子与可以经历互变异构的配体的配位如何在更高的层次上增加复杂性,这里表现为形成具有不同物理性质的异构分子组装。这些结果对于提高我们对化学和生物学中复杂性出现的理解具有重要意义。