4.7 Article

Spontaneous Resolution of Racemic Camphorates in the Formation of Three-Dimensional Metal-Organic Frameworks

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INORGANIC CHEMISTRY
卷 48, 期 14, 页码 6356-6358

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AMER CHEMICAL SOC
DOI: 10.1021/ic900918z

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  1. NIH [2 S06 GM063119-05]

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Reported here is a rare example of enantioselective processes between organic racemic ligands (DL-camphorates) with in situ formed chiral metal complexes. Such enantioselectivity leads to a double spontaneous resolution of two pairs of distinctly different racemates [the Lambda Delta-Zn(Htea) units and the DL-camphorate ligands] into two chiral three-dimensional frameworks containing only one enantiommeric form from each racemate. This work demonstrates unique enantioselectivity in the self-assembly of metal-organic frameworks containing multiple chiral features, which points to a new avenue for the preparation of chiral framework materials and for the resolution of racemates.

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