dc.creatorXu, Hong Lei
dc.creatorPopov, Ivan A.
dc.creatorTkachenko, Nikolay V.
dc.creatorWang, Zi Chuan
dc.creatorMuñoz-Castro, Alvaro
dc.creatorBoldyrev, Alexander I.
dc.creatorSun, Zhong Ming
dc.date.accessioned2023-05-24T22:00:04Z
dc.date.available2023-05-24T22:00:04Z
dc.date.created2023-05-24T22:00:04Z
dc.date.issued2020-09-21
dc.identifier1433-7851
dc.identifierhttps://repositorio.uss.cl/handle/uss/8001
dc.identifier10.1002/anie.202008276
dc.description.abstractIn this work, the largest heterometallic supertetrahedral clusters, [Zn6Ge16]4− and [Cd6Ge16]4−, were directly self-assembled through highly-charged [Ge4]4− units and transition metal cations, in which 3-center–2-electron σ bonding in Ge2Zn or Ge2Cd triangles plays a vital role in the stabilization of the whole structure. The cluster structures have an open framework with a large central cavity of diameter 4.6 Å for Zn and 5.0 Å for Cd, respectively. Time-dependent HRESI-MS spectra show that the larger clusters grow from smaller components with a single [Ge4]4− and ZnMes2 units. Calculations performed at the DFT level indicate a very large HOMO–LUMO energy gap in [M6Ge16]4− (2.22 eV), suggesting high kinetic stability that may offer opportunities in materials science. These observations offer a new strategy for the assembly of heterometallic clusters with high symmetry.
dc.languageeng
dc.relationAngewandte Chemie - International Edition
dc.titleσ-Aromaticity-Induced Stabilization of Heterometallic Supertetrahedral Clusters [Zn6Ge16]4− and [Cd6Ge16]4−
dc.typeArtículo


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