Thermodynamic Study of the  Tautomerism Schiff Base derived from para-aminophenol by Catalyst

Ortho-Methoxybenzylidene-para-hydroxyaniline, meta-Methoxybenzylidene-para-hydroxyaniline, and para-Hydroxybenzylidene-para-hydroxyaniline, as numbered 1,2,3, were synthesized by standard methods. The chemical structures of these compounds were confirmed previously by physical methods in addition to chemical tests. The tautomerism reactions of the above mentioned imine in this paper required the measurements of ultraviolet absorption spectra of imines under study. The tautomeric equilibrium constants of the Schiff bases under study were determined at five different temperatures ranging from 10°C to 50°C, facilitating the estimation of the equilibrium constants of the tautomerism reactions and the thermodynamic functions, namely ?G, ?H, and ?S, of the Schiff base tautomers.

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Publication Details

Journal
NTU Journal of Pure Sciences
Published
2025-10-12
DOI
https://doi.org/10.56286/emkdjg70
Primary Topic
Chemical Thermodynamics and Molecular Structure
Type
article
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article

Thermodynamic Study of the  Tautomerism Schiff Base derived from para-aminophenol by Catalyst

Asmaa Baker Al-Dabbagh
NTU Journal of Pure Sciences
Chemical Thermodynamics and Molecular Structure
article

Thermodynamic Study of the  Tautomerism Schiff Base derived from para-aminophenol by Catalyst

Asmaa Baker Al-Dabbagh
article en

Abstract

Ortho-Methoxybenzylidene-para-hydroxyaniline, meta-Methoxybenzylidene-para-hydroxyaniline, and para-Hydroxybenzylidene-para-hydroxyaniline, as numbered 1,2,3, were synthesized by standard methods. The chemical structures of these compounds were confirmed previously by physical methods in addition to chemical tests. The tautomerism reactions of the above mentioned imine in this paper required the measurements of ultraviolet absorption spectra of imines under study. The tautomeric equilibrium constants of the Schiff bases under study were determined at five different temperatures ranging from 10°C to 50°C, facilitating the estimation of the equilibrium constants of the tautomerism reactions and the thermodynamic functions, namely ?G, ?H, and ?S, of the Schiff base tautomers.

NTU Journal of Pure SciencesVol. 4(3)
Northern Technical University (IQ)
Openalex Percentile: Top 78%
Chemical Thermodynamics and Molecular Structure
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Thermodynamic Study of the  Tautomerism Schiff Base derived from para-aminophenol by Catalyst — Asmaa Baker Al-Dabbagh · NTU Journal of Pure Sciences (2025) | TGRS Research Map | TGRS