Bulletin des Sociétés Chimiques Belges · 1987 · 11 citations · 10 references
Natural SciencesChemistryOrganic ChemistryPhysical ChemistrySpectroscopyChemical BondingInfrared SpectroscopyIntermolecular ForcesMolecular SpectroscopySolvation EffectsSolvation TheoryAcid-base InteractionsInfrared Absorption SpectraInfrared Absorption SpectroscopyInfrared SpectraSolvent Effects On Absorption SpectraSolvent Effects On Electronic SpectraSolvent Effects On PkaSolvent Effects On Spectra
Abstract The interaction between nicotine and phenol derivatives has been studied by infrared spectrometry in solvents of low polarity. The enthalpies of complex formation ranged from 24 to 36 kJmol −1 and the Δv OH values from 440 to 580 cm −1 , indicating a rather strong interaction. The FT‐Infrared spectra (1100‐600 cm −1 ) strongly suggest that the interaction occurs at the N atom of the pyridine ring showing that hydrogen bond formation is governed by the accessibility of the lone pair of the base.
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Okuma Emile Kasende, Th. Zeegers‐Huyskens · The Journal of Physical Chemistry · 1984 · 50 citations
Natural Sciences, Chemistry, Physics +12