Ligand Substitution Experiments (AQA A Level Chemistry)
Revision Note
Ligand Substitution Experiments
Ligand Substitution Experiments
The factors that affect the colour formed for different transition metal ion solutions are:
type of ligand
change in oxidation state
co-ordination number
These colour changes can be observed by performing test tube reactions of metal aqua ions in test tubes with addition of different reagents
Examiner Tips and Tricks
It is important with test tube reactions to not only record the colour in your observations but also whether a solution or precipitate is formed.
Test tube reactions
Measure 2 cm3 of 1.0 mol dm−3 aqueous metal aqua ion solution and transfer into a test tube, held in the test tube rack
Using a dropping pipette, add the 1.0 mol dm −3 ammonia solution dropwise, and gently shake the test tube between drops and record any observations
Continue to add the 1.0 mol dm−3 ammonia solution and shake between additions and record any observations
This procedure can be repeated with different aqueous metal aqua ion solutions and reagents e.g. hydrochloric acid
Table showing factors affecting colour
The colour changes from light blue to a yellow-green when copper(II) is treated with concentrated hydrochloric acid. The green appearance is due to the presence of unreacted aqueous copper(II) ions
Addition of excess aqueous ammonia to the aqueous copper(II) ion results in a gorgeous deep blue complex
Bidentate and multidentate
Bidentate and multidentate
Complexes involving bidentate and even more so, multidentate ligands are more stable than those with only monodentate ligands in them
The underlying reason for this is that each multidentate ligand displaces more than one water molecule
This leads to an increase in the number of species present in the system, and therefore an increase in entropy
An increase in entropy makes the formation of the chelated complex more favourable
This is known as the chelate effect
Rate of substitution
UV/visible spectrophotometry could be used to compare the rate of ligand substitution of a metal aqua ion of monodentate and multidentate ligands
The Lambert-Beer law relates the absorbance to the concentration of coloured complex ions in solution
You don't need to recall this law for the exam but it can be used along with UV/visible spectrophotometer to show the mathematics behind working out the rate of substitution
A = ɛcl
A = absorbance, c = concentration, ɛ = molar extinction coefficient and l = path length (distance travelled by radiation through the solution)
Practical procedure
The initial concentration of the metal aqua ion solution is measured using the UV/visible spectrophotometer, often this can be a simpler colorimeter
An aqueous solution of monodentate ligand is added to the metal aqua ion solution
Every 30 seconds, 0.1 cm3 reaction mixture is extracted and diluted with 100 cm3 of water to stop the reaction
The sample is placed into a cuvette and radiation at the wavelength of maximum absorbance is passed through the sample
The absorbance is recorded
The process is repeated every 30 seconds for 300 seconds
A calibration curve of time against absorbance can then be plotted
The process can be repeated with the same metal aqua ion solution with a multidentate ligand
The molar extinction coefficient, ɛ, can be calculated and used to compare the rate of ligand substitution of monodentate to multidentate ligand
Examiner Tips and Tricks
Sometimes the solution is too dilute to give a sufficiently intense colour for the colorimeter to measure. In such cases a suitable ligand is first added (e.g. thiocyanate ions, SCN-) to give an intense colour.The visible range is scanned to find the most intense absorption frequency to pass through the solution of a fixed path length.
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