19F NMR Fingerprints: Identification of Neutral Organic Compounds in a Molecular Container | Zendy

Yanchuan Zhao | Zendy; Γεώργιος Μαρκόπουλος | Zendy; Timothy M. Swager | Zendy

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¹⁹F NMR Fingerprints: Identification of Neutral Organic Compounds in a Molecular Container

Author(s) -

Yanchuan Zhao,

Γεώργιος Μαρκόπουλος,

Timothy M. Swager

Publication year - 2014

Publication title -

journal of the american chemical society

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 7.115

H-Index - 612

eISSN - 1520-5126

pISSN - 0002-7863

DOI - 10.1021/ja504110f

Subject(s) - chemistry , analyte , chemical shift , fingerprint (computing) , molecule , molecular recognition , nuclear magnetic resonance spectroscopy , proton nmr , analytical chemistry (journal) , fluorine 19 nmr , chromatography , stereochemistry , organic chemistry , computer security , computer science

Improved methods for quickly identifying neutral organic compounds and differentiation of analytes with similar chemical structures are widely needed. We report a new approach to effectively "fingerprint" neutral organic molecules by using (19)F NMR and molecular containers. The encapsulation of analytes induces characteristic up- or downfield shifts of (19)F resonances that can be used as multidimensional parameters to fingerprint each analyte. The strategy can be achieved either with an array of fluorinated receptors or by incorporating multiple nonequivalent fluorine atoms in a single receptor. Spatial proximity of the analyte to the (19)F is important to induce the most pronounced NMR shifts and is crucial in the differentiation of analytes with similar structures. This new scheme allows for the precise and simultaneous identification of multiple analytes in a complex mixture.

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