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Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]

The dinuclear title complex, [Co(2)(C(5)H(7)O(2))(4)(μ-OH)(2)] or [Co(acac)(2)(μ-OH)](2), where acac is acetyl­acetonate, is centrosymmetric with half of the mol­ecule per asymmetric unit. The mol­ecular structure is a dimer of octa­hedrally coordinated Co(III) atoms with four O atoms from two chela...

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Autores principales: Richers, Casseday P., Bertke, Jeffery A., Rauchfuss, Thomas B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571372/
https://www.ncbi.nlm.nih.gov/pubmed/26396771
http://dx.doi.org/10.1107/S2056989015013663
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author Richers, Casseday P.
Bertke, Jeffery A.
Rauchfuss, Thomas B.
author_facet Richers, Casseday P.
Bertke, Jeffery A.
Rauchfuss, Thomas B.
author_sort Richers, Casseday P.
collection PubMed
description The dinuclear title complex, [Co(2)(C(5)H(7)O(2))(4)(μ-OH)(2)] or [Co(acac)(2)(μ-OH)](2), where acac is acetyl­acetonate, is centrosymmetric with half of the mol­ecule per asymmetric unit. The mol­ecular structure is a dimer of octa­hedrally coordinated Co(III) atoms with four O atoms from two chelating acac ligands and two O atoms from bridging hydroxide ligands. The crystal packing features weak C—H⋯O inter­actions between neighboring mol­ecules, leading to the formation of chains normal to the ac plane. The hydroxide H atoms are not involved in hydrogen bonding because of the bulky acac ligands. This is the first crystal structure reported of a dimeric transition metal bis-acac complex with OH(−) as the bridging group.
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spelling pubmed-45713722015-09-22 Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)] Richers, Casseday P. Bertke, Jeffery A. Rauchfuss, Thomas B. Acta Crystallogr E Crystallogr Commun Research Communications The dinuclear title complex, [Co(2)(C(5)H(7)O(2))(4)(μ-OH)(2)] or [Co(acac)(2)(μ-OH)](2), where acac is acetyl­acetonate, is centrosymmetric with half of the mol­ecule per asymmetric unit. The mol­ecular structure is a dimer of octa­hedrally coordinated Co(III) atoms with four O atoms from two chelating acac ligands and two O atoms from bridging hydroxide ligands. The crystal packing features weak C—H⋯O inter­actions between neighboring mol­ecules, leading to the formation of chains normal to the ac plane. The hydroxide H atoms are not involved in hydrogen bonding because of the bulky acac ligands. This is the first crystal structure reported of a dimeric transition metal bis-acac complex with OH(−) as the bridging group. International Union of Crystallography 2015-07-29 /pmc/articles/PMC4571372/ /pubmed/26396771 http://dx.doi.org/10.1107/S2056989015013663 Text en © Richers et al. 2015 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 Research Communications
Richers, Casseday P.
Bertke, Jeffery A.
Rauchfuss, Thomas B.
Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]
title Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]
title_full Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]
title_fullStr Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]
title_full_unstemmed Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]
title_short Crystal structure of di-μ-hydroxido-κ(4) O:O-bis[bis(acetyl­acetonato-κ(2) O,O′)cobalt(III)]
title_sort crystal structure of di-μ-hydroxido-κ(4) o:o-bis[bis(acetyl­acetonato-κ(2) o,o′)cobalt(iii)]
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571372/
https://www.ncbi.nlm.nih.gov/pubmed/26396771
http://dx.doi.org/10.1107/S2056989015013663
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