Issue 18, 2021

Alkali-regulated Fe6 and Fe18 molecular clusters and their structural transformation

Abstract

As a kind of metastable aggregation between iron ions and iron hydroxide precipitates, Fe clusters can only be isolated under narrow synthesis conditions. Here, two Fe clusters with different structural models, [Fe6(H2thmmg)6] (Fe6) and [Fe18O8(OH)8(H2thmmg)10] (Fe18), are constructed based on a rare N-tris(hydroxymethyl)methylglycine (H5thmmg) ligand. The cyclic Fe6 can be visualized as a “six-vane windmill” comprised of 6 Fe3+ and 6 H2thmmg3− ligands. Unlike the cyclic configuration of Fe6, the Fe18 cluster features a bricky structure like a “Chinese knot” coordinated by three species, H2thmmg3−, OH and O2−. It was obtained by adding more triethylamine to the reactive solution of Fe6 which yielded more coordinated species OH and O2−. Moreover, the conversion from Fe6 to Fe18 was successfully achieved by adding more triethylamine, realizing nuclearity enlargement and structural regulation of Fe clusters. Furthermore, the magnetic properties of Fe6 and Fe18 exhibit antiferromagnetism. This work reports two novel alkali-regulated Fe clusters and further realizes the transformation of nuclearity and structure, which provides some reference for the structural predesign and adjustment of metal nanoclusters.

Graphical abstract: Alkali-regulated Fe6 and Fe18 molecular clusters and their structural transformation

Supplementary files

Article information

Article type
Research Article
Submitted
15 Haz 2021
Accepted
22 Tem 2021
First published
23 Tem 2021

Inorg. Chem. Front., 2021,8, 4186-4191

Alkali-regulated Fe6 and Fe18 molecular clusters and their structural transformation

X. Li, Y. Zou, S. Han and G. Wang, Inorg. Chem. Front., 2021, 8, 4186 DOI: 10.1039/D1QI00750E

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