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Topic: Isolation of optical isomers  (Read 7186 times)

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mip

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Isolation of optical isomers
« on: June 04, 2005, 11:49:44 PM »
I did a prac on resolution of tris(ethylenediamine)cobalt(III) ions.  We had tris(ethylenediamine)cobalt(III) chloride trihydrate and reacted it in solution (at about 80 degrees C) with silver (+)-tartrate.  We isolated crystals of the (+)Co(en)3.(+)tart.Cl (ie the (+)(+)diastereoisomer).  We then dissolved these crystals in 5M HCl and added a solution of NaI.  We then added a few mL of ethanol to complete the precipitation of the (+)tris(ethylenediamine)cobalt(III) iodide.

In my prac report I have to include reasons for adding HCl and NaI and I don't really understand why we used HCl, was it to change the pH of the solution, and if so, why?

Any help on this would be much appreciated.  :)

mip

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Re:Isolation of optical isomers
« Reply #1 on: June 05, 2005, 10:26:13 PM »
Just incase anyone else was wondering, it turns out we dissolved the isomers in HCl as it is a conc. source of chloride ions and thus (somehow) increases the solubiltity of the crystal isomers... I hope that makes sense, Im exhausted!!!

Offline movies

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Re:Isolation of optical isomers
« Reply #2 on: June 05, 2005, 11:43:18 PM »
Maybe you just need a high ionic strength in solution to help solubilize the complex.

Just guessing though, my inorganic techniques are lacking.

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Re:Isolation of optical isomers
« Reply #3 on: June 06, 2005, 05:17:53 AM »
This is a classic Werner synthesis from 1912.
The complex is good soluble in water but only sparingly in medium concentrated HCl solution.
Moreover, the complex is unstable in  solution at RT, hence a precipitation should be fast

Werner, Ber. 45, 121 (1912)
Inorg. Synth. 2, 221-222, 223-225
Inorg. Synth. 6, 183-186
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