Dicobalt edetate
Dicobalt edetate | |
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Other names Kelocyanor | |
Identifiers | |
CAS number | 36499-65-7 |
PubChem | 71942 |
ChemSpider | 64951 |
Jmol-3D images | {{#if:C(CN(CC(=O)[O-])CC(=O)[O-])N(CC(=O)[O-])CC(=O)[O-].[Co+2].[Co+2][Co+2].[Co+2].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O|Image 1 Image 2 |
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Properties | |
Molecular formula | C10H12Co2N2O8.6H2O |
Molar mass | 406.08 g/mol 514.18 g/mol (hexahydrate) |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Dicobalt edetate is the coordination compound with the approximate formula Co2(EDTA)(H2O)6.
Solutions of this solid have been used in Europe as an antidote to cyanide poisoning.[1]
It is a derivative of the (non-natural) amino acid ethylenediaminetetraacetate.
Structure
The compound is polymeric in the crystalline form. Half of the Co2+ ions are bound to the EDTA2− and the other Co2+ ions are bound to four water ligands as well as carboxylate ligands on the [Co(EDTA)]2− entity.[2] In aqueous solution, depolymerization occurs to give [Co(EDTA)]2− and [Co(H2O)6]2+ ions, each of which is kinetically labile and has a high affinity for cyanide. Oxidants would convert the [Co(EDTA)]2− into [Co(EDTA)]−, which would be unreactive toward cyanide because this complex would be "inert."[3]
References
- ↑ Pickering WG (December 1985). "Cyanide toxicity and the hazards of dicobalt edetate". Br Med J (Clin Res Ed) 291 (6509): 1644. doi:10.1136/bmj.291.6509.1644-a. PMC 1418389. PMID 2866807.
- ↑ E. F. K. Mccandlish, T. K. Michael; Rose, N. J.; Neal, J. A.; Lingafelter, E. C.; Rose, N. J. (1978). "Comparison of the Structures and Aqueous Solutions of [(O-Phenylenediaminetetraacetato(2-)]Cobalt(II) and [Ethylenediaminetetraacetato(2-)]Cobalt(II)". Inorg. Chem. 17 (6): 1383–94. doi:10.1021/ic50184a001.
- ↑ Dwyer, F. P.; Garvan, F. L.; Kirschner, Stanley (1960). "Resolution of the Ethylenediaminetetracetatocobaltate(III) Ion". Inorg. Synth. Inorganic Syntheses 4: 192–4. doi:10.1002/9780470132371.ch61. ISBN 978-0-470-13237-1.