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Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/20645
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dc.contributor.authorLim, Jason Y. C.pt
dc.contributor.authorMarques, Igorpt
dc.contributor.authorFerreira, Lilianapt
dc.contributor.authorFelix, Vitorpt
dc.contributor.authorBeer, Paul D.pt
dc.date.accessioned2017-12-07T19:54:30Z-
dc.date.issued2016pt
dc.identifier.issn1359-7345pt
dc.identifier.urihttp://hdl.handle.net/10773/20645-
dc.description.abstractChiral halogen bonding (S)-BINOL-based receptors are demonstrated to enhance the enantioselective recognition and sensing of chiral anions compared to their hydrogen bonding analogues. Computational studies attribute this behaviour to the strict linearity of halogen bonding (XB) and steric environment conferred by the XB donor groups bridged by the (S)-BINOL motif.pt
dc.language.isoengpt
dc.publisherROYAL SOC CHEMISTRYpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147343/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147332/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F87520%2F2012/PTpt
dc.rightsrestrictedAccesspor
dc.subjectAMINO-ACIDSpt
dc.subjectRECEPTORSpt
dc.subjectCATALYSISpt
dc.subjectWATERpt
dc.subjectIONpt
dc.subjectEXPLORATIONpt
dc.subjectSENSORSpt
dc.subjectFIELDpt
dc.titleEnhancing the enantioselective recognition and sensing of chiral anions by halogen bondingpt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage5527pt
degois.publication.issue32pt
degois.publication.lastPage5530pt
degois.publication.titleCHEMICAL COMMUNICATIONSpt
degois.publication.volume52pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1039/c6cc01701kpt
dc.identifier.doi10.1039/c6cc01701kpt
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