Revue des Sciences Fondamentales Appliquées
Volume 8, Numéro 2, Pages 569-583
2016-05-01
Auteurs : Kasmi-mir S. . Elkebich M. . Dembahri Z. . Haouzi A. . Kirsch G. .
We describe the synthesis of new organic Schiff bases chromophores 5 containing a rhodanine-3- acetic as electron accepteur moiety. Imines 3 were obtained by a condensation reaction from a lead molecule, the aminothiazolinethione 1 with versatile commercial aldehydes. The structure of all the compounds obtained was determined by the spectroscopic methods (IR, 1H NMR and 13C NMR). The study of UV-Vis imines 3 and 5 in methanol exhibit the phenomenon of π delocalized electrons responsible for the bathochromic effect.
Aminothiazolinethione; iminomerocyanines; chromophores; rhodanine; bathochrome effect.
بوسالم أحلام
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عابد يوسف
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ص 117-132.
Yahia Zeghoudi
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pages 74-88.
Madani Abdelghani
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Bouchama Anis
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Hellal Abdelkader
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pages 42-55.
Said Houari Amel
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pages 257-268.
Madani Salim
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Mokhnache Kamel
.
Rouane Azeddine
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Charef Noureddine
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pages 001-009.