期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 21, 期 36, 页码 12581-12585出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201501486
关键词
asymmetric catalysis; chirality; linker exchange; metal-organic frameworks; vanadium
资金
- NSFC [21371119, 21431004, 21401128]
- 973 Program [2014CB932102, 2012CB8217]
- SSTC [14YF1401300]
Two chiral porous metal-organic frameworks (MOFs) were constructed from [VO(salen)]-derived dicarboxylate and dipyridine bridging ligands. After oxidation of V-IV to V-V, they were found to be highly effective, recyclable, and reusable heterogeneous catalysts for the asymmetric cyanosilylation of aldehydes with up to 95%ee. Solvent-assisted linker exchange (SALE) treatment of the pillared-layer MOF with [Cr(salen)Cl]- or [Al(salen)Cl]-derived dipyridine ligands led to the formation of mixed-linker metallosalen-based frameworks and incorporation of [Cr(salen)] enabled its use as a heterogeneous catalyst in the asymmetric epoxide ring-opening reaction.
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