Tautomerism in salicylidenebenzylamine

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

doi:10.1080/00387019208021526

Tautomerism in salicylidenebenzylamine

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

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Abstract

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.

Originalsprog	Engelsk
Artikelnummer	44
Tidsskrift	Spectroscopy Letters
Vol/bind	25
Udgave nummer	4
Sider (fra-til)	513-519
Antal sider	7
ISSN	0038-7010
DOI	https://doi.org/10.1080/00387019208021526
Status	Udgivet - 1992
Udgivet eksternt	Ja

Link til dokument

10.1080/00387019208021526

Citer dette

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title = "Tautomerism in salicylidenebenzylamine",

abstract = "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.",

author = "Kamounah, {Fadhil S.} and Shawkat, {Sawsan H.} and Salman, {Salman R.}",

year = "1992",

doi = "10.1080/00387019208021526",

language = "English",

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journal = "Spectroscopy Letters",

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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

SN - 0038-7010

VL - 25

SP - 513

EP - 519

JO - Spectroscopy Letters

JF - Spectroscopy Letters

IS - 4

M1 - 44

ER -