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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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 |
Sumario: | 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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