1973
DOI: 10.1002/prac.19733150203
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Spectrophotometric Study of α‐Nitroso‐β‐naphthol and its 3,6‐disulphonic acid (nitroso‐R‐Salt)

Abstract: The U. V. and visible absorption spectra of α‐nitroso‐β‐naphthol and nitroso‐R‐salt are recorded in solutions of varying pH. The U. V. bands are assigned to π → π* transition within the aromatic system while the visible bands are assigned to intramolecular charge transfer. The pK of both compounds are determined from spectrophotometric and pH measurements.

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Cited by 9 publications
(4 citation statements)
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“…The oximate may also be viewed as a substituted ortho-quinone. Quinones are well known CT acceptors [43,44], but oximates have also donor properties [45]( scheme 3).…”
Section: IIImentioning
confidence: 99%
“…The oximate may also be viewed as a substituted ortho-quinone. Quinones are well known CT acceptors [43,44], but oximates have also donor properties [45]( scheme 3).…”
Section: IIImentioning
confidence: 99%
“…The oximate may also be viewed as a substituted ortho-quinone. Quinones are well known CT acceptors [43,44], but oximates have also donor properties [45]( scheme 3).…”
Section: Brmentioning
confidence: 99%
“…Protonation constants of the investigated ketocyanines in the ground state have been determined by two methods, half-height method (HHM) 22 and limiting absorbance methods (LAM). 23 From the inflection point of the spectrophotometric titration curves, the ground state pK a -values were determined and listed in table 5 together with spectral maxima of different species. Protonation constants of the investigated ketocyanines in the first singlet excited state pK * a are determined by using Forster cycle.…”
Section: Acidochromic and Prototropic Equilibria Of The Investigated mentioning
confidence: 99%