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Topic: Rxn Mech.  (Read 9228 times)

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Offline arie

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Rxn Mech.
« on: May 16, 2007, 01:11:57 AM »
Hi every one, I've a question regarding this equation:



Does anyone of you have the idea that what happen to the one Cl that disappear?

Thank you.

Offline Borek

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Re: Rxn Mech.
« Reply #1 on: May 16, 2007, 02:29:20 AM »
There is some inconsistency here. As far as I understand that's simple complexation, yet you start with Ru(III) and end with Ru(II). Or am I missing something?
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Offline AWK

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Re: Rxn Mech.
« Reply #2 on: May 16, 2007, 03:04:28 AM »
Synthesis  proceeded in oil bath at 170-180 C. Organic compounds can be oxidized!
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Offline arie

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Re: Rxn Mech.
« Reply #3 on: May 16, 2007, 03:09:13 AM »
Dear Borek,

That's exactly why this equation puzzles me.

But I did manage to synthesis the product. I've done characterization using IR, CHNS and EDX.

I just do not understand how the rxn happen. So far no answer for my question, although I did done a lot of info searching in journal and text book. ???

The synthesis process carry out by refluxing these two compound in DMF for 8 hours.

Offline arie

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Re: Rxn Mech.
« Reply #4 on: May 16, 2007, 03:27:51 AM »
Synthesis  proceeded in oil bath at 170-180 C. Organic compounds can be oxidized!

So can you explain in detail what may happened to the Cl that disappear?

Thank you.

Offline Borek

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Re: Rxn Mech.
« Reply #5 on: May 16, 2007, 04:19:46 AM »
Organic compounds can be oxidized!

Nobody suggested otherwise. But it usually means some change in their structure or at least they become charged. I can't see nothing like that here - is there some byproduct not listed, or should I buy new glasses?
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Offline AWK

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Re: Rxn Mech.
« Reply #6 on: May 16, 2007, 04:27:04 AM »
Synthesis  proceeded in oil bath at 170-180 C. Organic compounds can be oxidized!

So can you explain in detail what may happened to the Cl that disappear?

Thank you.
HCl.
But you have DMF. It can hydrolyse to form formic acid and (CH3)2NH2Cl.
Since your synthesis is a redox reaction, at least part of bipyridil should be oxidized
AWK

Offline arie

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Re: Rxn Mech.
« Reply #7 on: May 16, 2007, 07:40:53 AM »


Dear Borek,
These are the procedures I went through to produce the product. I'm not sure whether got by-products, but AWK suggest the HCl,formic acid or (CH3)2NH2Cl formed.

I'll check again to see whether got these compound.

Dear AWK,
Thanks for your explanation. Actually my viva is on tomorrow. I'll try to understand your explanation and answer the question in case examiner test me.

By the way, do you have any references specially for this type of rxn?

Thank you!  :)


Offline AWK

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Re: Rxn Mech.
« Reply #8 on: May 16, 2007, 07:48:02 AM »
Original paper is published in Inorg. Chem. 1999, 38, 6298-6305
AWK

Offline arie

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Re: Rxn Mech.
« Reply #9 on: May 16, 2007, 07:54:24 AM »
Thank you. Unfortunately the library has closed. Anyway, thank you very much for your answer. you helped me a lot :)

Offline arie

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Re: Rxn Mech.
« Reply #10 on: May 17, 2007, 10:41:42 AM »
Hi, what analytical skills or spectroscopy i can use to determine the oxidation state of Ru is II?

Offline Sam (NG)

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Re: Rxn Mech.
« Reply #11 on: May 22, 2007, 04:13:52 PM »
You could measure the magnetic susceptibility of the starting material and the product (you know that the first is Ru (III)) using the Gouy Method, or you could use Electron Paramagnetic Resonance Spectroscopy.

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