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Transmission of electronic effects in 4‐aryl‐2,6‐diphenylpyrylium perchlorates and related compounds
Author(s) -
Rasała Danuta,
Bąk Tomasz,
Kolehmainen Erkki,
Styrcz Stanisław,
Gawinecki Ryszard
Publication year - 1996
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/(sici)1099-1395(199609)9:9<631::aid-poc829>3.0.co;2-x
Subject(s) - substituent , chemistry , aryl , moiety , chemical shift , resonance (particle physics) , stereochemistry , computational chemistry , medicinal chemistry , photochemistry , organic chemistry , alkyl , physics , particle physics
Substituent effects on the 13 C NMR spectra of 4‐aryl‐2,6‐diphenylpyrylium and 1‐methyl‐4‐aryl‐2,6‐diphenylpyridinium perchlorates and 4‐aryl‐2,6‐diphenylpyridines were investigated. The dual substituent parameter approach indicates that the resonance contribution to the carbon chemical shifts in the para position to the substituent in the 4‐aryl moiety is comparable to that for 4‐R‐biphenyls. Although heterocyclic moieties jointed at the para position with respect to the substituent in the 4‐aryl group differ in their deactivating power, they diminish the resonance term to the same extent in each series. This may result in conformational variations of the compounds studied. AM1 calculations were used to explain the chemical shifts observed.