Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes

A series of heteroleptic chelate copper(II) complexes of the type [Cu(L)(acac)]X where acac = acetylacetonate; L = N,N′-1,6-bis(2-fluorophenyl)-2,5-diazahexane; X=CIO4-, BPh4-, PF6-, and BF4- have been prepared and characterized by elemental analyses, IR and UV-Vis spectroscopies, and molar conducta...

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Main Authors: Hamid Golchoubian, Hakimeh Fazilati
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Journal of Spectroscopy
Online Access:http://dx.doi.org/10.1155/2013/470427
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author Hamid Golchoubian
Hakimeh Fazilati
author_facet Hamid Golchoubian
Hakimeh Fazilati
author_sort Hamid Golchoubian
collection DOAJ
description A series of heteroleptic chelate copper(II) complexes of the type [Cu(L)(acac)]X where acac = acetylacetonate; L = N,N′-1,6-bis(2-fluorophenyl)-2,5-diazahexane; X=CIO4-, BPh4-, PF6-, and BF4- have been prepared and characterized by elemental analyses, IR and UV-Vis spectroscopies, and molar conductance measurements. The prepared complexes are fairly soluble in a large number of organic solvents and show positive solvatochromism. Among the complexes [Cu(L)(acac)]ClO4, it is demonstrated the most solvatochromism. A multiparametric equation has been utilized to explain the solvent effect on the d-d transition of the complexes using SPSS/PC software. To explore the mechanism of interaction between solvent molecules and the complexes, different solvent parameters such as DN, AN, α, ET(30), π*, and β using stepwise multiple linear regression (SMLR) method were employed. The results demonstrated that the donor power of the solvent plays the most important role in the solvatochromism of the compounds.
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spelling doaj-art-5a00f0e31ee6479cbf91b2142b26b0312025-02-03T07:24:26ZengWileyJournal of Spectroscopy2314-49202314-49392013-01-01201310.1155/2013/470427470427Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) ComplexesHamid Golchoubian0Hakimeh Fazilati1Department of Inorganic Chemistry, University of Mazandaran, Babolsar 47416-95447, IranDepartment of Inorganic Chemistry, University of Mazandaran, Babolsar 47416-95447, IranA series of heteroleptic chelate copper(II) complexes of the type [Cu(L)(acac)]X where acac = acetylacetonate; L = N,N′-1,6-bis(2-fluorophenyl)-2,5-diazahexane; X=CIO4-, BPh4-, PF6-, and BF4- have been prepared and characterized by elemental analyses, IR and UV-Vis spectroscopies, and molar conductance measurements. The prepared complexes are fairly soluble in a large number of organic solvents and show positive solvatochromism. Among the complexes [Cu(L)(acac)]ClO4, it is demonstrated the most solvatochromism. A multiparametric equation has been utilized to explain the solvent effect on the d-d transition of the complexes using SPSS/PC software. To explore the mechanism of interaction between solvent molecules and the complexes, different solvent parameters such as DN, AN, α, ET(30), π*, and β using stepwise multiple linear regression (SMLR) method were employed. The results demonstrated that the donor power of the solvent plays the most important role in the solvatochromism of the compounds.http://dx.doi.org/10.1155/2013/470427
spellingShingle Hamid Golchoubian
Hakimeh Fazilati
Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes
Journal of Spectroscopy
title Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes
title_full Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes
title_fullStr Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes
title_full_unstemmed Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes
title_short Effect of Counterion on the Solvatochromic Properties of Heteroleptic Chelate Copper(II) Complexes
title_sort effect of counterion on the solvatochromic properties of heteroleptic chelate copper ii complexes
url http://dx.doi.org/10.1155/2013/470427
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