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Apicophilicity of substituent groups and the structures of some trigonal bipyramidal trifluoromethylphosphoranes
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1974
Year
Low Temperature N.m.rNatural SciencesSpectroscopyFluorous SynthesisSpectra-structure CorrelationOrganic ChemistryElectronegative ParametersMain Group ChemistryTrigonal Bipyramidal TrifluoromethylphosphoranesQuantum ChemistryChemistryEquatorial SubstitutionSubstituent GroupsSpectroscopic PropertyBiophysics
Low temperature n.m.r. spectroscopy is capable of distinguishing axial and equatorial substitution in trigonal bipyramidal trifluoromethylphosphoranes allowing the establishment of a partial ‘apicophilicity’ series for some substituent groups which appears to be based chiefly on inductive rather than mesomeric or electronegative parameters of the groups.