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

Research output: Contribution to journal › Journal article › Research › peer-review

16 Citations (Scopus)

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.

Original language	English
Article number	44
Journal	Spectroscopy Letters
Volume	25
Issue number	4
Pages (from-to)	513-519
Number of pages	7
ISSN	0038-7010
DOIs	https://doi.org/10.1080/00387019208021526
Publication status	Published - 1992
Externally published	Yes

Access to Document

10.1080/00387019208021526

Citation Styles

@article{ef48d867f9a74377b649e704e5cbcff1,

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",

volume = "25",

pages = "513--519",

journal = "Spectroscopy Letters",

issn = "0038-7010",

publisher = "Taylor \& Francis Inc.",

number = "4",

}

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

SN - 0038-7010

VL - 25

SP - 513

EP - 519

JO - Spectroscopy Letters

JF - Spectroscopy Letters

IS - 4

M1 - 44

ER -