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Topic: Complex Problem  (Read 3108 times)

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Offline Dolphinsiu

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Complex Problem
« on: December 14, 2006, 02:00:18 AM »
Complex stereoisomers for tetraamminedichlorocobalt(III) has cis- and trans- forms.

Why cis-form is violet and trans-form is green?
Why the green one has lower solubility?

I only know that it is the same energy level for d-d splitting according to crystal field theory.
But why trans-form still abosrbs higher frequency of light than cis-form?
Is this related to the difference of their spatial arrangement?

Please help ! Thanks a lot!

Offline Donaldson Tan

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Re: Complex Problem
« Reply #1 on: December 14, 2006, 08:30:05 AM »
Why the green one has lower solubility?

It has definitely to do with its trans-structure. How does it affect bonding with the solvent?

But why trans-form still abosrbs higher frequency of light than cis-form?

How does the trans-arrangement enhance the d-d splitting?
"Say you're in a [chemical] plant and there's a snake on the floor. What are you going to do? Call a consultant? Get a meeting together to talk about which color is the snake? Employees should do one thing: walk over there and you step on the friggin� snake." - Jean-Pierre Garnier, CEO of Glaxosmithkline, June 2006

Offline Dolphinsiu

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Re: Complex Problem
« Reply #2 on: December 14, 2006, 10:10:27 AM »
Trans-complex is symmetric, so it has low solubility in water.
and Cl- are located at the two dz^2 of complex which has higher energy level
so it enhance d-d splitting, thereby absorbing higher frequency of light

But cis-complex is asymetric, so it has high solubility in water
and Cl- are located at dx^2-y^2 and dz^2 of complex respectively which hs lower energy level
thereby it absorbs low frequency of light.

Are these correct?
« Last Edit: December 14, 2006, 10:16:46 AM by Dolphinsiu »

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