Enantiopure trigonal bipyramidal coordination cages templated by in situ self-organized D2h-symmetric anions.
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ABSTRACT: The control of a molecule's geometry, chirality, and physical properties has long been a challenging pursuit. Our study introduces a dependable method for assembling D3-symmetric trigonal bipyramidal coordination cages. Specifically, D2h-symmetric anions, like oxalate and chloranilic anions, self-organize around a metal ion to form chiral-at-metal anionic complexes, which template the formation of D3-symmetric trigonal bipyramidal coordination cages. The chirality of the trigonal bipyramid is determined by the point chirality of chiral amines used in forming the ligands. Additionally, these cages exhibit chiral selectivity for the included chiral-at-metal anionic template. Our method is broadly applicable to various ligand systems, enabling the construction
SUBMITTER: Guo S
PROVIDER: S-EPMC11224320 | biostudies-literature | 2024 Jul
REPOSITORIES: biostudies-literature
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