The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions

<p>Abstract</p> <p>Background</p> <p>The importance of the isatinic quinolyl hydrazones arises from incorporating the quinoline ring with the indole ring. Quinoline ring has therapeutic and biological activities whereas, the indole ring occurs in Jasmine flowers and Ora...

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Main Authors: Mousa Marwa A, El-Shetary Bashir A, El-Inany Gaber A, Seleem Hussein S, Hanafy Fatin I
Format: Article
Language:English
Published: BMC 2011-04-01
Series:Chemistry Central Journal
Online Access:http://journal.chemistrycentral.com/content/5/1/20
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spelling doaj-081b7bad24884de080c08a9cc6b795462021-08-02T06:08:22ZengBMCChemistry Central Journal1752-153X2011-04-01512010.1186/1752-153X-5-20The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ionsMousa Marwa AEl-Shetary Bashir AEl-Inany Gaber ASeleem Hussein SHanafy Fatin I<p>Abstract</p> <p>Background</p> <p>The importance of the isatinic quinolyl hydrazones arises from incorporating the quinoline ring with the indole ring. Quinoline ring has therapeutic and biological activities whereas, the indole ring occurs in Jasmine flowers and Orange blossoms. As a ligand, the isatin moiety is potentially ambidentate and can coordinate the metal ions either through its lactam or lactim forms. In a previous study, the ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions has been studied. As continuation of our interest, the present study is planned to check the ligational behavior of an isatinic quinolyl hydrazone.</p> <p>Results</p> <p>New homo- and heteroleptic copper(II)- complexes were obtained from the reaction of an isatinic quinolyl hydrazone (HL) with several copper(II)- salts <it>viz. </it>Clˉ, Brˉ, NO<sub>3</sub>ˉ, ClO<sub>4</sub><sup>-</sup>, SO<sub>4</sub><sup>2- </sup>and AcO<sup>-</sup>. The obtained complexes have O<sub>h</sub>, T<sub>d </sub>and D<sub>4h</sub>- symmetry and fulfill the strong coordinating ability of Clˉ, Brˉ, NO<sub>3</sub>ˉ and SO<sub>4</sub><sup>2- </sup>anions. Depending on the type of the anion, the ligand coordinates the copper(II)- ions either through its lactam (NO<sub>3</sub>ˉ and ClO<sub>4</sub><sup>-</sup>) or lactim (the others) forms.</p> <p>Conclusion</p> <p>The effect of anion for the same metal ion is obvious from either the geometry of the isolated complexes (O<sub>h</sub>, T<sub>d </sub>and D<sub>4h</sub>) or the various modes of bonding. Also, the obtained complexes fulfill the strong coordinating ability of Clˉ, Brˉ, NO<sub>3</sub>ˉ and SO<sub>4</sub><sup>2- </sup>anions in consistency with the donor ability of the anions. In case of copper(II)- acetate, a unique homoleptic complex (<b>5</b>) was obtained in which the AcO<sup>- </sup>anion acts as a base enough to quantitatively deprotonate the hydrazone. The isatinic hydrazone uses its lactim form in most complexes.</p> http://journal.chemistrycentral.com/content/5/1/20
collection DOAJ
language English
format Article
sources DOAJ
author Mousa Marwa A
El-Shetary Bashir A
El-Inany Gaber A
Seleem Hussein S
Hanafy Fatin I
spellingShingle Mousa Marwa A
El-Shetary Bashir A
El-Inany Gaber A
Seleem Hussein S
Hanafy Fatin I
The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions
Chemistry Central Journal
author_facet Mousa Marwa A
El-Shetary Bashir A
El-Inany Gaber A
Seleem Hussein S
Hanafy Fatin I
author_sort Mousa Marwa A
title The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions
title_short The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions
title_full The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions
title_fullStr The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions
title_full_unstemmed The ligational behavior of an isatinic quinolyl hydrazone towards copper(II)- ions
title_sort ligational behavior of an isatinic quinolyl hydrazone towards copper(ii)- ions
publisher BMC
series Chemistry Central Journal
issn 1752-153X
publishDate 2011-04-01
description <p>Abstract</p> <p>Background</p> <p>The importance of the isatinic quinolyl hydrazones arises from incorporating the quinoline ring with the indole ring. Quinoline ring has therapeutic and biological activities whereas, the indole ring occurs in Jasmine flowers and Orange blossoms. As a ligand, the isatin moiety is potentially ambidentate and can coordinate the metal ions either through its lactam or lactim forms. In a previous study, the ligational behavior of a phenolic quinolyl hydrazone towards copper(II)- ions has been studied. As continuation of our interest, the present study is planned to check the ligational behavior of an isatinic quinolyl hydrazone.</p> <p>Results</p> <p>New homo- and heteroleptic copper(II)- complexes were obtained from the reaction of an isatinic quinolyl hydrazone (HL) with several copper(II)- salts <it>viz. </it>Clˉ, Brˉ, NO<sub>3</sub>ˉ, ClO<sub>4</sub><sup>-</sup>, SO<sub>4</sub><sup>2- </sup>and AcO<sup>-</sup>. The obtained complexes have O<sub>h</sub>, T<sub>d </sub>and D<sub>4h</sub>- symmetry and fulfill the strong coordinating ability of Clˉ, Brˉ, NO<sub>3</sub>ˉ and SO<sub>4</sub><sup>2- </sup>anions. Depending on the type of the anion, the ligand coordinates the copper(II)- ions either through its lactam (NO<sub>3</sub>ˉ and ClO<sub>4</sub><sup>-</sup>) or lactim (the others) forms.</p> <p>Conclusion</p> <p>The effect of anion for the same metal ion is obvious from either the geometry of the isolated complexes (O<sub>h</sub>, T<sub>d </sub>and D<sub>4h</sub>) or the various modes of bonding. Also, the obtained complexes fulfill the strong coordinating ability of Clˉ, Brˉ, NO<sub>3</sub>ˉ and SO<sub>4</sub><sup>2- </sup>anions in consistency with the donor ability of the anions. In case of copper(II)- acetate, a unique homoleptic complex (<b>5</b>) was obtained in which the AcO<sup>- </sup>anion acts as a base enough to quantitatively deprotonate the hydrazone. The isatinic hydrazone uses its lactim form in most complexes.</p>
url http://journal.chemistrycentral.com/content/5/1/20
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