2 Dimethylglyoxime + Ni 2+- Ni(DMG) 2 + 2 H + The Ni(DMG) 2 complex (MW 288.9 g/mole) is stable to heat and is unusually hydrophobic; it will dry quickly in an oven at 110-120 o C to yield a pure substance whose weight can be used to calculate the nickel content of the original sample. The Gravimetric Determination of Nickel INTRODUCTION Nickel(II) forms a precipitate with the organic compound dimethylglyoxime, C4H6(NOH)2. The formation of the red chelate occurs quantitatively in a solution in which the pH is buffered in the range of 5 to 9. The chelation reaction that occurs is illustrated below. Assignments: 1. The geometry of nickel dimethyl glyoxime complex is. Octahedral c. Square planar d. The percent of nickel in Ni-DMG complex is. NOTE: DMG is insoluble in water and is used as a 1% solution in ethanol. A slight excess of the reagent is needed to precipitate all the Ni 2+, but a large excess should be avoided because of the possible precipitation of the DMG (white precipitate) itself due to its low solubility in water. The estimation of nickel is the presence of cobalt, iron or copper 11, 12. Thus, various methods have been developed to help eliminate this problem. One of them is the common, well known, sensitive and simple method which shows the complexometric reaction between nickel and dimethyglyoxime 13. To obtain a gravimetric determination of nickel using dimethylglyoxime: Weigh and measure a sample so that not over 100 mg. Of nickel present. Add 10 cc’s of nitric acid.5 to.1 grams of potassium chlorate and digest on the steam plate adding more potassium chlorate if necessary to effect solution. Evaporate to dryness.
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| Names | |
|---|---|
| IUPAC name nickel;N-[(Z)-3-nitrosobut-2-en-2-yl]hydroxylamine | |
| Other names | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| EC Number | |
PubChemCID | |
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| Properties | |
| C8H14N4NiO4 | |
| Molar mass | 288.917 g·mol−1 |
| Appearance | red solid |
| Density | 1.698 g/cm3 |
| Hazards | |
| GHS pictograms | |
| 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). | |
| Infobox references | |
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[edit]
Nickel(II) 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[edit]
Estimation Of Nickel As Ni Dmg In Mac
- ^Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN978-0-08-037941-8.
- ^Donald E. Williams, Gabriele Wohlauer, R. E. Rundle (1959). 'Crystal Structures of Nickel and Palladium Dimethylglyoximes'. J. Am. Chem. Soc. 81: 755–756. doi:10.1021/ja01512a066.CS1 maint: uses authors parameter (link)
- ^Tschugaeff, Lev (1905). 'Über ein neues, empfindliches Reagens auf Nickel' [About a new, sensitive reagent on nickel] (PDF). Berichte der deutschen chemischen Gesellschaft (in German). 38 (3): 2520–2522. doi:10.1002/cber.19050380317.
| Names | |
|---|---|
| IUPAC name | |
Other names
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| Identifiers | |
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| ChEMBL | |
| ChemSpider |
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| ECHA InfoCard | 100.002.201 |
| EC Number | |
PubChemCID | |
| RTECS number |
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| UNII | |
CompTox Dashboard(EPA) | |
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| Properties | |
| C4H8N2O2 | |
| Molar mass | 116.120 g·mol−1 |
| Appearance | White/Off White Powder |
| Density | 1.37 g/cm3 |
| Melting point | 240 to 241 °C (464 to 466 °F; 513 to 514 K) |
| Boiling point | decomposes |
| low | |
| Structure | |
| 0 | |
| Hazards | |
| Main hazards | Toxic, Skin/Eye Irritant |
| Safety data sheet | External MSDS |
| GHS pictograms | |
| GHS Signal word | Danger |
| H228, H301 | |
| P210, P240, P241, P264, P270, P280, P301+310, P321, P330, P370+378, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Related compounds | |
| Hydroxylamine salicylaldoxime | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Dimethylglyoxime is a chemical compound described by the formula CH3C(NOH)C(NOH)CH3. Its abbreviation is dmgH2 for neutral form, and dmgH for anionic form, where H stands for hydrogen. This colourless solid is the dioxime derivative of the diketone butane-2,3-dione (also known as diacetyl). DmgH2 is used in the analysis of palladium or nickel. Its coordination complexes are of theoretical interest as models for enzymes and as catalysts. Many related ligands can be prepared from other diketones, e.g. benzil.
Preparation[edit]
Dimethylglyoxime can be prepared from butanone first by reaction with ethyl nitrite to give biacetyl monoxime. The second oxime is installed using sodium hydroxylamine monosulfonate:[1]
Estimation Of Nickel As Ni Dmg In Windows
Complexes[edit]
Dimethylglyoxime is used to detect and quantify nickel, which forms the bright red complex nickel bis(dimethylglyoximate) (Ni(dmgH)2). The reaction was discovered by L. A. Chugaev in 1905.[2]
Cobalt complexes have also received much attention. In chloro(pyridine)cobaloxime[3] the macrocycle [dmgH]22− mimics the macrocyclic ligand found in vitamin B12.
References[edit]
- ^Semon, W. L.; Damerell, V. R. (1930). 'Dimethylglyoxime'. Organic Syntheses. 10: 22. doi:10.15227/orgsyn.010.0022.CS1 maint: multiple names: authors list (link)
- ^Lev Tschugaeff (1905). 'Über ein neues, empfindliches Reagens auf Nickel'. Berichte der Deutschen Chemischen Gesellschaft. 38 (3): 2520–2522. doi:10.1002/cber.19050380317.
- ^Girolami, G.. S.; Rauchfuss, T.B.; Angelici, R. J. (1999). Synthesis and Technique in Inorganic Chemistry: A Laboratory Manual (3rd ed.). pp. 213–215.