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{μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate

The title dinuclear copper complex, [Cu(2)(C(15)H(15)N(6)O)Cl(2)(CH(3)OH)(2)]ClO(4), was prepared by the reaction of copper(II) chloride with bis­[1-(2-pyrid­yl)ethyl­idene]carbonohydrazide in the presence of sodium perchlorate in a methanol solution. It features a mono-deprotonated bis-tridentate l...

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Autor principal: Huang, Wei
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971001/
https://www.ncbi.nlm.nih.gov/pubmed/21578103
http://dx.doi.org/10.1107/S1600536809040471
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author Huang, Wei
author_facet Huang, Wei
author_sort Huang, Wei
collection PubMed
description The title dinuclear copper complex, [Cu(2)(C(15)H(15)N(6)O)Cl(2)(CH(3)OH)(2)]ClO(4), was prepared by the reaction of copper(II) chloride with bis­[1-(2-pyrid­yl)ethyl­idene]carbonohydrazide in the presence of sodium perchlorate in a methanol solution. It features a mono-deprotonated bis-tridentate ligand, which coordinates to two independent Cu(II) ions, one of which is coordinated by pyridyl N, hydrazyl N and carbonyl O atoms. The second Cu(II) ion is coordinated by the pyridyl N and two hydrazyl N atoms from different hydrazyl groups. The coordination environments of both Cu(II) ions are completed by a chloride ion and a methanol mol­ecule. The dihedral angle between the pyridyl groups is 27.46 (10)°. The crystal packing is stabilized by O—H⋯O(perchlorate), O—H⋯Cl and N—H⋯Cl hydrogen bonding.
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spelling pubmed-29710012010-12-30 {μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate Huang, Wei Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title dinuclear copper complex, [Cu(2)(C(15)H(15)N(6)O)Cl(2)(CH(3)OH)(2)]ClO(4), was prepared by the reaction of copper(II) chloride with bis­[1-(2-pyrid­yl)ethyl­idene]carbonohydrazide in the presence of sodium perchlorate in a methanol solution. It features a mono-deprotonated bis-tridentate ligand, which coordinates to two independent Cu(II) ions, one of which is coordinated by pyridyl N, hydrazyl N and carbonyl O atoms. The second Cu(II) ion is coordinated by the pyridyl N and two hydrazyl N atoms from different hydrazyl groups. The coordination environments of both Cu(II) ions are completed by a chloride ion and a methanol mol­ecule. The dihedral angle between the pyridyl groups is 27.46 (10)°. The crystal packing is stabilized by O—H⋯O(perchlorate), O—H⋯Cl and N—H⋯Cl hydrogen bonding. International Union of Crystallography 2009-10-10 /pmc/articles/PMC2971001/ /pubmed/21578103 http://dx.doi.org/10.1107/S1600536809040471 Text en © Wei Huang 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Metal-Organic Papers
Huang, Wei
{μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate
title {μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate
title_full {μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate
title_fullStr {μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate
title_full_unstemmed {μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate
title_short {μ-1,5-Bis[(E)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(II)] perchlorate
title_sort {μ-1,5-bis[(e)-1-(2-pyrid­yl)ethyl­idene]carbonohydrazidato(1−)}bis­[chlorido­methano­lcopper(ii)] perchlorate
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971001/
https://www.ncbi.nlm.nih.gov/pubmed/21578103
http://dx.doi.org/10.1107/S1600536809040471
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