4.7 Article

Chiral Metal Organic Framework Decorated with TEMPO Radicals for Sequential Oxidation/Asymmetric Cyanation Catalysis

Journal

INORGANIC CHEMISTRY
Volume 57, Issue 16, Pages 9786-9789

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.8b01630

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Funding

  1. National Natural Science Foundation of China [21522104, 21431004, 21620102001]
  2. National Key Basic Research Program of China [2016YFA0203400]
  3. Key Project of Basic Research of Shanghai [17JC1403100, 18JC1413200]
  4. Shanghai Eastern Scholar Program

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A chiral porous metal organic framework (MOF) decorated with radicals has been successfully constructed by cocrystallizing achiral (2,2,6,6-tetramethyl-piperidin-1-yl)oxyl (TEMPO)-substituted tricarboxylate and enantiopure VO(salen)-derived dipyridine ligands. The chiral MOF can function as an efficient heterogeneous catalyst for the sequential alcohol oxidation/asymmetric cyanation of aldehyde reactions with enhanced activity and enantioselectivity compared to the homogeneous counterpart.

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