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Topic: Match splitting parameter with chromium complex  (Read 2903 times)

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Offline Rutherford

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Match splitting parameter with chromium complex
« on: March 16, 2014, 10:28:02 AM »
How to solve the attached problem?

I know that the cyanide group will cause the biggest splitting 26,600, but what about the rest? Why has CrF62- a bigger splitting than Cr(H2O)63+? I know that they have different oxidation states of Cr, but how does it cause the difference?

Offline kriggy

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Re: Match splitting parameter with chromium complex
« Reply #1 on: March 16, 2014, 12:35:19 PM »
The oxidation number of metal atom is also involved in splitting of D orbitals. So if we say that Δof M2+ is 1 then Δ for M3+ is about 1,6 and for M4+ its 1,9.
Im not sure why is that I cant find it in any of my notes, so if anyone knows plz share

Offline Rutherford

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Re: Match splitting parameter with chromium complex
« Reply #2 on: March 16, 2014, 01:12:20 PM »
Difference in ligand nature vs. the difference in oxidation number. Which one will prevail, I don't think is easy to tell.

Offline kriggy

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Re: Match splitting parameter with chromium complex
« Reply #3 on: March 16, 2014, 01:46:30 PM »
They both are involved  so if you have [M(CN)6]2- and [M(CN)6]3- and M is the same metal then [M(CN)6]2- will have greter value of Δ. Or at least according to my book

Offline Rutherford

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Re: Match splitting parameter with chromium complex
« Reply #4 on: March 16, 2014, 02:31:07 PM »
Okay. Now, I could just use some explanation why is it so.

Offline kriggy

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Re: Match splitting parameter with chromium complex
« Reply #5 on: March 16, 2014, 03:45:41 PM »
Ok found it:
By increasing the oxidation number of cental atom (and its positive charge) you also increase the atraction between nucleus and electrons in ligands which then increase the repulsion between the electrons in ligands and electrons in central atom and then the Δ.

Offline Rutherford

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Re: Match splitting parameter with chromium complex
« Reply #6 on: March 16, 2014, 04:07:06 PM »
Good. Thank you.

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