Tautomerism in salicylidenebenzylamine

Fadhil S. Kamounah, Sawsan H. Shawkat, Salman R. Salman

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Resumé

The UV spectra of substituted salicylidene benzylamine schiff bases were studied in four solvents. It was found that substituents which increase the electronic effect and not the steric compression effect in these compounds increase the percentage of the keto form. The intensity (i.e. % keto) of the keto band which occurs at > 400 nm in the UV spectra increases in polar solvents.
OriginalsprogEngelsk
Artikelnummer44
TidsskriftSpectroscopy Letters
Vol/bind25
Udgave nummer4
Sider (fra-til)513-519
Antal sider7
ISSN0038-7010
DOI
StatusUdgivet - 1992
Udgivet eksterntJa

Citer dette

Kamounah, F. S., Shawkat, S. H., & Salman , S. R. (1992). Tautomerism in salicylidenebenzylamine. Spectroscopy Letters, 25(4), 513-519. [44]. https://doi.org/10.1080/00387019208021526
Kamounah, Fadhil S. ; Shawkat, Sawsan H. ; Salman , Salman R. / Tautomerism in salicylidenebenzylamine. I: Spectroscopy Letters. 1992 ; Bind 25, Nr. 4. s. 513-519.
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Kamounah, FS, Shawkat, SH & Salman , SR 1992, 'Tautomerism in salicylidenebenzylamine' Spectroscopy Letters, bind 25, nr. 4, 44, s. 513-519. https://doi.org/10.1080/00387019208021526

Tautomerism in salicylidenebenzylamine. / Kamounah, Fadhil S.; Shawkat, Sawsan H.; Salman , Salman R.

I: Spectroscopy Letters, Bind 25, Nr. 4, 44, 1992, s. 513-519.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

TY - JOUR

T1 - Tautomerism in salicylidenebenzylamine

AU - Kamounah, Fadhil S.

AU - Shawkat, Sawsan H.

AU - Salman , Salman R.

PY - 1992

Y1 - 1992

N2 - The UV spectra of substituted salicylidene benzylamine schiff bases were studied in four solvents. It was found that substituents which increase the electronic effect and not the steric compression effect in these compounds increase the percentage of the keto form. The intensity (i.e. % keto) of the keto band which occurs at > 400 nm in the UV spectra increases in polar solvents.

AB - The UV spectra of substituted salicylidene benzylamine schiff bases were studied in four solvents. It was found that substituents which increase the electronic effect and not the steric compression effect in these compounds increase the percentage of the keto form. The intensity (i.e. % keto) of the keto band which occurs at > 400 nm in the UV spectra increases in polar solvents.

U2 - 10.1080/00387019208021526

DO - 10.1080/00387019208021526

M3 - Journal article

VL - 25

SP - 513

EP - 519

JO - Spectroscopy Letters

JF - Spectroscopy Letters

SN - 0038-7010

IS - 4

M1 - 44

ER -