Proton NMR studies of dihalogenated phenyl benzamides : two-dimensional higher quantum methodologies

The scalar coupled proton NMR spectra of many organic molecules possessing more than one phenyl ring are generally complex due to degeneracy of transitions arising from the closely resonating protons, in addition to several short- and long-range couplings experienced by each proton. Analogous situat...

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Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 47(2009), 8 vom: 15. Aug., Seite 684-92
1. Verfasser: Manjunatha Reddy, G N (VerfasserIn)
Weitere Verfasser: Nayak, Susanta Kumar, Guru Row, T N, Suryaprakash, N
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article
Beschreibung
Zusammenfassung:The scalar coupled proton NMR spectra of many organic molecules possessing more than one phenyl ring are generally complex due to degeneracy of transitions arising from the closely resonating protons, in addition to several short- and long-range couplings experienced by each proton. Analogous situations are generally encountered in derivatives of halogenated benzanilides. Extraction of information from such spectra is challenging and demands the differentiation of spectrum pertaining to each phenyl ring and the simplification of their spectral complexity. The present study employs the blend of independent spin system filtering and the spin-state selective detection of single quantum (SQ) transitions by the two-dimensional multiple quantum (MQ) methodology in achieving this goal. The precise values of the scalar couplings of very small magnitudes have been derived by double quantum resolved experiments. The experiments also provide the relative signs of heteronuclear couplings. Studies on four isomers of dihalogenated benzanilides are reported in this work
Beschreibung:Date Completed 16.09.2009
Date Revised 08.07.2009
published: Print
Citation Status PubMed-not-MEDLINE
ISSN:1097-458X
DOI:10.1002/mrc.2449