Spectroscopic Study of Tautomerism in Substituted Naphtylidineanilenes
- 1 June 1996
- journal article
- research article
- Published by Taylor & Francis in Spectroscopy Letters
- Vol. 29 (4) , 659-666
- https://doi.org/10.1080/00387019608007059
Abstract
New substituted naphtylidineaniline schiff bases were prepared. Their UV-visible spectra were run in different solvents with different polarity ranging from protic, aprotic and non polar. The two bands above 430 nm were assigned to the keto form, their molar extinction coefficient was used to calculate the keto form of those anils of 2-hydroxy-naphthalene-1-carbal-dehyde.Keywords
This publication has 12 references indexed in Scilit:
- Tautomerism in 2‐hydroxy‐1‐naphthaldehyde schiff bases in solution and the solid state investigated using 13C NMR spectroscopyMagnetic Resonance in Chemistry, 1993
- Tautomerism in Salicylidene BenzylamineSpectroscopy Letters, 1992
- Spectroscopic Study of Tautomerism In Dihydroxy Substituted Schiff BasesSpectroscopy Letters, 1991
- Studies of Tautomerism in 2-Hydroxynaphthaldehyde Schiff Bases by Multinuclear Magnetic ResonanceSpectroscopy Letters, 1991
- Spectroscopic studies of the photochromic molecule N-(2-hydroxybenzylidene)aniline and its photoproductThe Journal of Physical Chemistry, 1990
- Tautomerism in Chlorinated O-Hydroxyschiff Bases: Effect of Chlorine Atom SubstitutionSpectroscopy Letters, 1989
- Deuterium isotope effects on 13C nuclear shielding as a measure of tautomeric equilibriaMagnetic Resonance in Chemistry, 1982
- Spectroscopic and Kinetic Studies of the Photochromism of N-Salicylideneanilines and Related CompoundsBulletin of the Chemical Society of Japan, 1977
- Spectroscopic studies of keto–enol equilibria. Part XIII.15N-substituted iminesJournal of the Chemical Society B: Physical Organic, 1971
- Nuclear Magnetic Resonance Studies of Keto-Enol Equilibria. IV. Naphthalene DerivativesJournal of the American Chemical Society, 1963