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[2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide

The title Fe(III) complex, [Fe(C(22)H(32)N(4)O(2))]I, contains a six-coordinate FeN(4)O(2) cation in which the ligand is a reduced Schiff base resulting from the NaBH(4) reduction of the condensation product between salicylaldehyde and 1,5,8,12-tetra­azadodecane. In spite of the increased flexibilit...

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Detalles Bibliográficos
Autores principales: Assey, Gervas, Butcher, Ray J., Gultneh, Yilma, Yisgedu, Teshome
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979518/
https://www.ncbi.nlm.nih.gov/pubmed/21579344
http://dx.doi.org/10.1107/S1600536810018787
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author Assey, Gervas
Butcher, Ray J.
Gultneh, Yilma
Yisgedu, Teshome
author_facet Assey, Gervas
Butcher, Ray J.
Gultneh, Yilma
Yisgedu, Teshome
author_sort Assey, Gervas
collection PubMed
description The title Fe(III) complex, [Fe(C(22)H(32)N(4)O(2))]I, contains a six-coordinate FeN(4)O(2) cation in which the ligand is a reduced Schiff base resulting from the NaBH(4) reduction of the condensation product between salicylaldehyde and 1,5,8,12-tetra­azadodecane. In spite of the increased flexibility of the saturated backbone of the ligand compared to the Schiff base from which it was synthesized, the complex adopts a cis-FeN(4)O(2) conformation for the phenolic O-atom donors, which contrasts with the trans conformation adopted by the analogous ClO(4) (−) salt [Yisgedu et al. (2009 ▶). J. Chem. Crystallogr. 39, 315–319]. In addition to extensive N—H⋯I hydrogen bonding between the amine H atoms and the anion there is a weak C—H⋯I inter­action.
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spelling pubmed-29795182010-12-30 [2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide Assey, Gervas Butcher, Ray J. Gultneh, Yilma Yisgedu, Teshome Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title Fe(III) complex, [Fe(C(22)H(32)N(4)O(2))]I, contains a six-coordinate FeN(4)O(2) cation in which the ligand is a reduced Schiff base resulting from the NaBH(4) reduction of the condensation product between salicylaldehyde and 1,5,8,12-tetra­azadodecane. In spite of the increased flexibility of the saturated backbone of the ligand compared to the Schiff base from which it was synthesized, the complex adopts a cis-FeN(4)O(2) conformation for the phenolic O-atom donors, which contrasts with the trans conformation adopted by the analogous ClO(4) (−) salt [Yisgedu et al. (2009 ▶). J. Chem. Crystallogr. 39, 315–319]. In addition to extensive N—H⋯I hydrogen bonding between the amine H atoms and the anion there is a weak C—H⋯I inter­action. International Union of Crystallography 2010-05-26 /pmc/articles/PMC2979518/ /pubmed/21579344 http://dx.doi.org/10.1107/S1600536810018787 Text en © Assey et al. 2010 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
Assey, Gervas
Butcher, Ray J.
Gultneh, Yilma
Yisgedu, Teshome
[2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide
title [2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide
title_full [2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide
title_fullStr [2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide
title_full_unstemmed [2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide
title_short [2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide
title_sort [2,2′-(2,6,9,13-tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(iii) iodide
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979518/
https://www.ncbi.nlm.nih.gov/pubmed/21579344
http://dx.doi.org/10.1107/S1600536810018787
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