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dc.contributor.authorZhao, Yanchuan
dc.contributor.authorSwager, Timothy M
dc.date.accessioned2018-04-30T15:19:22Z
dc.date.available2018-04-30T15:19:22Z
dc.date.issued2015-03
dc.date.submitted2015-01
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/115088
dc.description.abstractThe rapid detection and differentiation of chiral compounds is important to synthetic, medicinal, and biological chemistry. Palladium complexes with chiral pincer ligands are demonstrated to have utility in determining the chirality of various amines. The binding of enantiomeric amines induces distinct ¹⁹F NMR shifts of the fluorine atoms appended on the ligand that defines a chiral environment around palladium. It is further demonstrated that this method has the ability to evaluate the enantiomeric composition and discriminate between enantiomers with chiral centers several carbons away from the binding site. The wide detection window provided by optimized chiral chemosensors allows the simultaneous identification of as many as 12 chiral amines. The extraordinary discriminating ability of this method is demonstrated by the resolution of chiral aliphatic amines that are difficult to separate using chiral chromatography.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (Grant GM095843)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jacs.5b00556en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceProf. Swager via Erja Kajosaloen_US
dc.titleSimultaneous Chirality Sensing of Multiple Amines by ¹⁹F NMRen_US
dc.typeArticleen_US
dc.identifier.citationZhao, Yanchuan, and Timothy M. Swager. “Simultaneous Chirality Sensing of Multiple Amines by ¹⁹F NMR.” Journal of the American Chemical Society 137, 9 (February 2015): 3221–3224 © 2015 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.contributor.approverSwager, Timothy Men_US
dc.contributor.mitauthorZhao, Yanchuan
dc.contributor.mitauthorSwager, Timothy M
dc.relation.journalJournal of the American Chemical Societyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsZhao, Yanchuan; Swager, Timothy M.en_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_POLICYen_US


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