COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES

A series of Schiff Bases of Ni(II) and Cu(II) using acetylacetone (acac), salicylaldehyde (sal), ethylenediamine (en), and o-phenylendiarnine (dabe) were prepared and characterized. The electronic spectra of some copper chelates in various organic solvents depend strongly on the solvent used and the...

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Format: Article
Language:English
Published: University of Tehran 1999-12-01
Series:Journal of Sciences, Islamic Republic of Iran
Online Access:https://jsciences.ut.ac.ir/article_31309_2538d141a69a158645d94157d0eecd23.pdf
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description A series of Schiff Bases of Ni(II) and Cu(II) using acetylacetone (acac), salicylaldehyde (sal), ethylenediamine (en), and o-phenylendiarnine (dabe) were prepared and characterized. The electronic spectra of some copper chelates in various organic solvents depend strongly on the solvent used and the d-d band of Cu(II) shifts to red with the increase of the Donor Number (DN) of solvent. The color changes from blue to green are observed. The mechanism for solvatochromism is discussed in terms of conformational changes and solvent coordination. Among the nickel complexes, Ni (saloph) is brownish red in chloroform and green in pyridine, probably due to the coordination of two pyridine molecules
format Article
id doaj-art-29e30a79e4474f3aad24c51207d017ff
institution OA Journals
issn 1016-1104
2345-6914
language English
publishDate 1999-12-01
publisher University of Tehran
record_format Article
series Journal of Sciences, Islamic Republic of Iran
spelling doaj-art-29e30a79e4474f3aad24c51207d017ff2025-08-20T02:25:51ZengUniversity of TehranJournal of Sciences, Islamic Republic of Iran1016-11042345-69141999-12-0110431309COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXESA series of Schiff Bases of Ni(II) and Cu(II) using acetylacetone (acac), salicylaldehyde (sal), ethylenediamine (en), and o-phenylendiarnine (dabe) were prepared and characterized. The electronic spectra of some copper chelates in various organic solvents depend strongly on the solvent used and the d-d band of Cu(II) shifts to red with the increase of the Donor Number (DN) of solvent. The color changes from blue to green are observed. The mechanism for solvatochromism is discussed in terms of conformational changes and solvent coordination. Among the nickel complexes, Ni (saloph) is brownish red in chloroform and green in pyridine, probably due to the coordination of two pyridine moleculeshttps://jsciences.ut.ac.ir/article_31309_2538d141a69a158645d94157d0eecd23.pdf
spellingShingle COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES
Journal of Sciences, Islamic Republic of Iran
title COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES
title_full COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES
title_fullStr COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES
title_full_unstemmed COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES
title_short COMPARATIVE STUDIES OF SOLVATOCHROMISM BEHAVIOUR OF COPPER(I1) AND NICKEL(I1) SCHIFF BASE COMPLEXES
title_sort comparative studies of solvatochromism behaviour of copper i1 and nickel i1 schiff base complexes
url https://jsciences.ut.ac.ir/article_31309_2538d141a69a158645d94157d0eecd23.pdf