JOURNAL ARTICLE
Proton magnetic resonance spectra of some disubstituted naphthalenes
Vittorio LucchiniPeter R. Wells
Year: 1977 Journal: Organic Magnetic Resonance Vol: 10 (1)Pages: 112-114 Publisher: Wiley
Abstract
Abstract The chemical shifts and coupling constants for the ring protons of nine disubstituted naphthalenes (mainly halogenonitre compounds) in carbon tetrachloride solutions have been obtained by analysis and computer simulation of their 100 MHz magnetic resonance spectra. Substituent effects are essentially additive except when a strong π‐donor group is in direct conjugation with a strong π‐acceptor group.
Keywords:
Substituent Proton magnetic resonance Chemical shift Ring (chemistry) Carbon tetrachloride Spectral line Coupling constant Chemistry Proton Acceptor Group (periodic table) Resonance (particle physics) Nuclear magnetic resonance Proton NMR Computational chemistry Physical chemistry Stereochemistry Organic chemistry Physics Atomic physics Condensed matter physics
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0.60
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8
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0.61
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Citation History
Topics
Molecular spectroscopy and chirality
Physical Sciences → Chemistry → Spectroscopy
Photochemistry and Electron Transfer Studies
Physical Sciences → Chemistry → Physical and Theoretical Chemistry
Electron Spin Resonance Studies
Life Sciences → Biochemistry, Genetics and Molecular Biology → Biophysics
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