Summary: Colorful aqueous complexes of nickel are made using ammonia, ethylene diamine and dimethylglyoxime ligands.
Hazards:
Nickel compounds are considered cancer suspect agents. Use care.
Substituents at the 2,9 positions confer protection for the attached metal, inhibiting the binding of multiple equivalents of the phenanthroline. Phen itself form complexes of the type M(phen) 3Cl 2 when treated with metal dihalides (M = Fe, Co, Ni). By contrast, neocuproine and bathocuproine form 1:1 complexes such as Ni(neo/batho-cuproine.
Chemicals and Solutions:
0.1M Nickel sulfate, NiSO4 https://cleverstars573.weebly.com/blog/reg-cleaner-for-mac.
Dmg converter mac. Conc. Ammonium hydroxide, NH4OH
25 % Ethylene diamine in ethanol
1% Dimethylglyoxime in ethanol
Materials: Download sierra dmg.
stirring rods
5 hydrometer cylinders
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Stirring rod
Beakers or crystallizing dishes
Procedure:
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In a large hydrometer cylinder place 100 mL 0.1M NiSO4 (this is the reference solution).
In a second large hydrometer place 200 mL 0.1M NiSO4. Add 20 mL of conc. NH4OH and stir to get the blue color of nickel ammine.
Pour half the nickel ammine into another large hydrometer and add ethylene diamine solution dropwise to get purple/lavender color.
Pour half the nickel ethylene diamine solution into a small hydrometer and add the DMG solution dropwise to form the red precipitate. Dmg drive free download.
Hint:
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Any green precipitate formation is due to Ni(OH)2 precipitate. (Add more ammonia to make it go away.)
Make the ethylene diamine solution fresh if there are crystals present in the solution or if itâs more than a year old. The ethylene diamine will oxidize with time. Test prior to class.
Discussion:
Ni(H2O)6+2 + 6NH3(aq) ---> Ni(NH3)6+2 + 6H2O
green (octahedral) blue (octahedral)
Ni(NH3)6+2 + 3en ----> Ni(en)3+2 + 6NH3
blue (octahedral) purple (octahedral)
Ni(en)32+ + 2DMG ---> Ni(DMG)2
purple (octahedral) red ppt. (square planar)
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