Chemistry:Nickel bis(dimethylglyoximate)
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| Names | |
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| IUPAC name
nickel;N-[(Z)-3-nitrosobut-2-en-2-yl]hydroxylamine
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| Other names
Bis(butanedione dioximato)nickel
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C8H14N4NiO4 | |
| Molar mass | 288.917 g·mol−1 |
| Appearance | red solid |
| Density | 1.698 g/cm3 |
| Hazards | |
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| GHS Signal word | Warning |
| H315, H317, H319, H335, H351 | |
| P201, P202, P261, P264, P271, P272, P280, P281, P302+352, P304+340, P305+351+338, P308+313, P312, P321, P332+313, P333+313, P337+313, P362, P363, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
Nickel bis(dimethylglyoximate) is the coordination complex with the formula Ni[ONC(CH3)C(CH3)NOH]2. The compound is a bright red solid. It achieved prominence for its use in the qualitative analysis of nickel.[1]
Structure
The geometry of the nickel(II) ion is square planar.[2] It is surrounded by two equivalents of the conjugate base (dmgH−) of dimethylglyoxime (dmgH2). The pair of organic ligands are joined through hydrogen bonds to give a macrocyclic ligand. The complex is distinctively colored and insoluble leading to its use as a chelating agent in the gravimetric analysis of nickel.
The use of dimethylglyoxime as a reagent to detect nickel was reported by L. A. Chugaev in 1905.[3]
References
- ↑ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
- ↑ Donald E. Williams; Gabriele Wohlauer; R. E. Rundle (1959). "Crystal Structures of Nickel and Palladium Dimethylglyoximes". J. Am. Chem. Soc. 81 (3): 755–756. doi:10.1021/ja01512a066.
- ↑ Tschugaeff, Lev (1905). "Über ein neues, empfindliches Reagens auf Nickel" (in de). Berichte der Deutschen Chemischen Gesellschaft 38 (3): 2520–2522. doi:10.1002/cber.19050380317. https://zenodo.org/record/1426158.
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