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(2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)

The title salt, [K(C(18)H(36)N(2)O(6))][Co(C(2)H(4))(4)], is one of only two known homoleptic ethyl­enemetalates. The cation and anion are well separated, which gives an unperturbed tetra­hedral anion as is expected for a formally Co(−I) d (10) metal center. The considerable elongation of the C=C bo...

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Autores principales: Brennessel, William W., Ellis, John E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470144/
https://www.ncbi.nlm.nih.gov/pubmed/23125588
http://dx.doi.org/10.1107/S1600536812038287
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author Brennessel, William W.
Ellis, John E.
author_facet Brennessel, William W.
Ellis, John E.
author_sort Brennessel, William W.
collection PubMed
description The title salt, [K(C(18)H(36)N(2)O(6))][Co(C(2)H(4))(4)], is one of only two known homoleptic ethyl­enemetalates. The cation and anion are well separated, which gives an unperturbed tetra­hedral anion as is expected for a formally Co(−I) d (10) metal center. The considerable elongation of the C=C bonds of the ethyl­ene ligands [average 1.401 (6) Å], relative to that of free ethyl­ene (1.333 Å), is consistent with metal→π* back-bonding models. One arm of the 2.2.2-cryptand (4,7,13,16,21,24-hexa­oxa-1,10-diaza­bicyclo­[8.8.8]hexa­cosa­ne) complexant is disordered and was modeled over two positions with a refined occupancy ratio of 0.559 (2):0.441 (2). In the crystal, the cationic K(2.2.2-cryptand) units are linked via C—H⋯O hydrogen bonds, forming inversion dimers. There are no other significant inter­molecular inter­actions in the crystal structure.
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spelling pubmed-34701442012-11-02 (2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I) Brennessel, William W. Ellis, John E. Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title salt, [K(C(18)H(36)N(2)O(6))][Co(C(2)H(4))(4)], is one of only two known homoleptic ethyl­enemetalates. The cation and anion are well separated, which gives an unperturbed tetra­hedral anion as is expected for a formally Co(−I) d (10) metal center. The considerable elongation of the C=C bonds of the ethyl­ene ligands [average 1.401 (6) Å], relative to that of free ethyl­ene (1.333 Å), is consistent with metal→π* back-bonding models. One arm of the 2.2.2-cryptand (4,7,13,16,21,24-hexa­oxa-1,10-diaza­bicyclo­[8.8.8]hexa­cosa­ne) complexant is disordered and was modeled over two positions with a refined occupancy ratio of 0.559 (2):0.441 (2). In the crystal, the cationic K(2.2.2-cryptand) units are linked via C—H⋯O hydrogen bonds, forming inversion dimers. There are no other significant inter­molecular inter­actions in the crystal structure. International Union of Crystallography 2012-09-12 /pmc/articles/PMC3470144/ /pubmed/23125588 http://dx.doi.org/10.1107/S1600536812038287 Text en © Brennessel and Ellis 2012 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
Brennessel, William W.
Ellis, John E.
(2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)
title (2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)
title_full (2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)
title_fullStr (2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)
title_full_unstemmed (2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)
title_short (2.2.2-Cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−I)
title_sort (2.2.2-cryptand)potassium tetra­kis­(η(2)-ethyl­ene)cobaltate(−i)
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470144/
https://www.ncbi.nlm.nih.gov/pubmed/23125588
http://dx.doi.org/10.1107/S1600536812038287
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