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Machine Learning Guided Assembly of a Nested Gd20@Gd32 @Ni36 Cluster via Urea Controlled Carbonate Release

Von Wiley-VCH zur Verfügung gestellt

A nested three-shell cluster Gd52Ni36 featuring a carbonate-templated dodecahedral Gd20 core was synthesized via a urea-mediated slow-release strategy. The mechanism of cluster formation was studied and the synthesis was optimized through a machine learning–guided high-throughput screening of 780 reaction conditions.


Abstract

Lanthanide-based polyhedral clusters are of great interest due to their unique geometries and functional properties, but their controlled synthesis remains a major challenge. Here, we report a nested three-shell cluster, [Gd52Ni36(MeIDA)36(OH)114(CO3)12 (H2O)48]·(ClO4)18·(H2O)21 (Gd52Ni36 , H2MeIDA = N-Methyliminodiacetic acid), achieved by using urea as a slow-release carbonate source to direct the formation of a dodecahedral inner shell. Single-crystal X-ray diffraction reveals a unique Gd20@Gd32@Ni36 arrangement, with the innermost Gd20 forming a Platonic dodecahedron templated by carbonate. A machine learning–guided, high-throughput synthesis platform enabled the exploration of 780 reaction conditions, uncovering key parameters and phase boundaries governing cluster formation. This work demonstrates data-driven strategies can accelerate the discovery of complex lanthanide architectures.

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