Journal of the Chemical Society. Perkin transactions II p. 123 - 126 (1986)
Update date:2022-07-29
Topics: Electronic absorption spectra
Hallas, Geoffrey
Marsden, Richard
Hepworth, John D.
Mason, Donald
Monoazo dyes containing a terminal morpholino group absorp hypsochromically in comparison with their piperidino counterparts as a result of electron withdrawal by the oxygen atom.Similar shifts are observed with related dyes possessing other γ-heteroatoms in the donor group.In acid solution, protonation takes place at the β-azo nitrogen atom (azonium tautomer) and at the terminal nitrogen atom (ammonium tautomer) to an extent which depends on the inductive effect of the γ-substituent.
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