Tautomerism of 2-hydroxynaphthaldehyde Schiff bases

Fadhil S. Kamounah, Liudmil Antonov, Daniela Nedeltcheva, Walter Fabian

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Resumé

A UV–Vis spectroscopic study based on the recently developed chemometric approach for quantitative analysis of undefined mixtures is performed on a series of donor and acceptor substituted Schiff bases of 2-hydroxynaphthaldehydes. In CCl4 solution all compounds preferentially exist as the phenol tautomer independent of the nature of the respective substituent. With increasing polarity the tautomeric equilibrium is shifted towards the quinone form. In CHCl3 and, especially, ethanol a clear distinction between the effect of donors (stabilization of the quinone form) and acceptors (stabilization of the phenol tautomer) is evident. Ab initio calculations including solvent effects via the polarized continuum model of solvation as well as the supermolecule approach are used to rationalize the experimental findings.
OriginalsprogEngelsk
Artikelnummer34
TidsskriftJournal of the Chemical Society. Perkin Transactions 2 (2001)
Vol/bind6
Sider (fra-til)1173-1179
Antal sider7
ISSN1472-779X
DOI
StatusUdgivet - 2000
Udgivet eksterntJa

Citer dette

Kamounah, Fadhil S. ; Antonov, Liudmil ; Nedeltcheva, Daniela ; Fabian, Walter. / Tautomerism of 2-hydroxynaphthaldehyde Schiff bases. I: Journal of the Chemical Society. Perkin Transactions 2 (2001). 2000 ; Bind 6. s. 1173-1179.
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Tautomerism of 2-hydroxynaphthaldehyde Schiff bases. / Kamounah, Fadhil S.; Antonov, Liudmil; Nedeltcheva, Daniela; Fabian, Walter.

I: Journal of the Chemical Society. Perkin Transactions 2 (2001), Bind 6, 34, 2000, s. 1173-1179.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

TY - JOUR

T1 - Tautomerism of 2-hydroxynaphthaldehyde Schiff bases

AU - Kamounah, Fadhil S.

AU - Antonov, Liudmil

AU - Nedeltcheva, Daniela

AU - Fabian, Walter

PY - 2000

Y1 - 2000

N2 - A UV–Vis spectroscopic study based on the recently developed chemometric approach for quantitative analysis of undefined mixtures is performed on a series of donor and acceptor substituted Schiff bases of 2-hydroxynaphthaldehydes. In CCl4 solution all compounds preferentially exist as the phenol tautomer independent of the nature of the respective substituent. With increasing polarity the tautomeric equilibrium is shifted towards the quinone form. In CHCl3 and, especially, ethanol a clear distinction between the effect of donors (stabilization of the quinone form) and acceptors (stabilization of the phenol tautomer) is evident. Ab initio calculations including solvent effects via the polarized continuum model of solvation as well as the supermolecule approach are used to rationalize the experimental findings.

AB - A UV–Vis spectroscopic study based on the recently developed chemometric approach for quantitative analysis of undefined mixtures is performed on a series of donor and acceptor substituted Schiff bases of 2-hydroxynaphthaldehydes. In CCl4 solution all compounds preferentially exist as the phenol tautomer independent of the nature of the respective substituent. With increasing polarity the tautomeric equilibrium is shifted towards the quinone form. In CHCl3 and, especially, ethanol a clear distinction between the effect of donors (stabilization of the quinone form) and acceptors (stabilization of the phenol tautomer) is evident. Ab initio calculations including solvent effects via the polarized continuum model of solvation as well as the supermolecule approach are used to rationalize the experimental findings.

U2 - 10.1039/B000798F

DO - 10.1039/B000798F

M3 - Journal article

VL - 6

SP - 1173

EP - 1179

JO - Royal Chemical Society. Journal. Perkin Transactions 2

JF - Royal Chemical Society. Journal. Perkin Transactions 2

SN - 1472-779X

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ER -