Synthesis and characterization of Ni(DMG)2
(Nickel (ii) dimethylglyoxime ) complex
GROUP 2
Sibongisiwe Shongwe 202002403
Happy Mabuza 202002010
Temvelo Vilane 202004446
Temazwide Nxumalo 202003920
CHE402| 08 February 2024
Aim: To synthesize and characterize Nickel (ii) Dimethylglyoxime complex.
Introduction
Transition metal complexes play a crucial role in various fields including catalysis, material
science and coordination chemistry. Dimethylglyoxime acts as a bidentate ligand forming an
stable complexes with Nickel ions and is used to detect presence of Nickel in solution. Nickel
reacts with Dimethylglyoxime to form a red precipitate of Nickel Dimethylglyoxime
complex. The Nickel Dimethylglyoxime complex (NiC8H14N4O4) is used in gravimetric
analysis of Nickel.
Fig 1. Nickel (ii) Dimethylglyoxime complex
Synthesis of Ni(DMG)2
M = n/V(l)
0.1 M = n / 0.25
n = 0.1 × 0.25 = 0.025
n = m/ Mw
m = n× Mw
m = 0.025× 280.86 = 7.0215 g
7.0215 g of Nickel sulphate (0.1M) was dissolved in 250 ml of distilled water and 20 mL of
the solution was taken for the synthesis
Equation for synthesis
NiSO4 •7H2O + 2C4H8O2N2 Ni( C4H7O2N2)2 + H2SO4 + 7H2O
Results
Ni(DMG)2
Weight = 0.044g
Molar mass = 288.92 g/mol
Percentage yield = (actual yield/ theoretical yield) × 100%
Theoretical yield = number of moles × molecular mass
Number of moles
1. NiSO4 • 7H2O = m/ Mm
n = 7.0215 g / 280.86 g/mol
n = 7.0215 / 280.86 = 0.025 mol
1 mol (NiSO4•7H2O) = 1 mol Ni( C4H7O2N2)2
Meaning 0.025 mol NiSO4•7H2O = 0.025 mol Ni(C4H7O2N2)2
2. C4H8O2N2 = m / Mm. Mm= 116.12 g/ mol
m=p×V
m = 1.37 g/ cm3 × 30 ml
m = 41.1 g
Then; n = m/ Mm
n = 41.1 / 116.12 = 0.354 mol
2mol (C4N8O2N2) = 1 mol Ni (C4H7O2N2)2
Meaning ; 0.354 mol = 0.177 mol
Number of moles of Ni(C4H7O2N2)2 = 0.025mol
Theoretical yield = 0.025 × 288.92 = 7.223 g
% yield = ( 0.044g / 7.223g) ×100%
= 0.61%
Characterization of Ni( DMG)2
Solubility testing of Nickel (ii) dimethylglyoxime complex show that:
(i) Water - insoluble
(ii) Methanol - partially soluble
(iii) Ethanol - soluble
(iv) Chloroform - partially soluble
Discussion
References
A. Dakhel, Y. Ahmed and F. Henari, Opt. Mater., 2006, 28, 925-929.
Q. Hu, G. Yang, Y. Zhao and J. Yin, Anal. Bioanal. Chem., 2003, 375, 831-835.