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[ni(dmg)2]2+



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  1. Ni(dmg)2 2 Release
Ni(dmg)2
Nickel bis(dimethylglyoximate)
Names
IUPAC name
nickel;N-[(Z)-3-nitrosobut-2-en-2-yl]hydroxylamine
Other names
Identifiers
3D model (JSmol)
ChemSpider
EC Number
PubChemCID
  • InChI=1S/2C4H8N2O2.Ni/c2*1-3(5-7)4(2)6-8;/h2*5,7H,1-2H3;/b2*4-3-;
  • CC(=C(C)N=O)NO.CC(=C(C)N=O)NO.[Ni]
Properties
C8H14N4NiO4
Molar mass288.917 g·mol−1
Appearancered solid
Density1.698 g/cm3
Hazards
GHS pictograms
GHS Signal wordWarning
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]

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Structure[edit]

Hour

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.

In contrast, a relatively larger reaction enthalpy for Cu(DMG)2 formation from chemically relevant species is found than that of Ni(DMG)2 because of the greater binding enthalpy of Ni(H2O)62+ than that of Cu(H2O)62+. In dimers, Ni(DMG)2 is found to be 6 kcal mol–1 more stable than Cu(DMG)2 due to a greater extent of dispersive interactions. Its abbreviation is dmgH 2 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). DmgH 2 is used in the analysis of palladium or nickel. Its coordination complexes are of theoretical interest as models for enzymes and as.

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The use of dimethylglyoxime as a reagent to detect nickel was reported by L. https://tiocamohy.tistory.com/1. A. Chugaev in 1905.[3]

References[edit]

  1. ^Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN978-0-08-037941-8.
  2. ^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)
  3. ^Lev Tschugaeff (1905). 'Über ein neues, empfindliches Reagens auf Nickel'. Berichte der deutschen chemischen Gesellschaft. 38 (3): 2520–2522. doi:10.1002/cber.19050380317.
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Ni(dmg)2 2 Release

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