Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4252
Title: Chiral Separation of Styrene Oxides Supported by Enantiomeric Tetrahedral Neutral Pd(II) Cages
Authors: RAJASEKAR, PRABHAKARAN
Pandey, Swechchha
Ferrara, Joseph D.
Campo, Mark Del
Magueres, Pierre Le
BOOMISHANKAR, RAMAMOORTHY
Dept. of Chemistry
Keywords: Hydrolytic Kinetic Resolution
Catalytic Synthesis
Terminal Epoxides
Efficient
TOC-DEC-2019
2019
Issue Date: Nov-2019
Publisher: American Chemical Society
Citation: Inorganic Chemistry, 58(22), 15017-15020.
Abstract: The separation of enantiomers is of considerable importance in the preparation of the compounds of biological interests, catalysis, and drug development. Here, we report a novel enantioseparation of styrene epoxides (SOs) resolved in the presence of a pair of enantio-enriched tetrahedral cages. Chiral neutral cages of formula [(Pd3X*)4(C6O4Cl2)6] ([X*]3– = RRR- or SSS-[PO(N(*CH(CH3)Ph)3]3–) are constructed from Pd3 building units supported by tris(imido)phosphate trianions and chloranilate linkers. These cages exhibit considerable enantioselective separation capabilities toward a series of styrene epoxides via a crystallization inclusion method. A highest enantiomeric excess (ee) value of up to 80% is achieved for the (R)-4-fluorostyrene oxide.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4252
https://doi.org/10.1021/acs.inorgchem.9b02389
ISSN: 0020-1669
1520-510X
Appears in Collections:JOURNAL ARTICLES

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.