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Topic: Reasons for amorphous peak in NMR?  (Read 3254 times)

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Offline Misa

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Reasons for amorphous peak in NMR?
« on: October 09, 2016, 08:37:08 AM »
I have been working with compounds derived from 1,10-Phenanthroline. For products with different functional groups, solvents and reaction conditions, I am seeing an amorphous peak for the protons meta to the nitrogens instead of the expected dd.

What could be reasons for this distortion?

The compounds are known to π stack and I was wondering if that could be a factor?

Any ideas would be greatly appreciated !!  :D :D

Offline TheUnassuming

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Re: Reasons for amorphous peak in NMR?
« Reply #1 on: October 10, 2016, 08:59:56 AM »
Are the other peaks in your spectra clean?  When you search the literature for similarly substituted compounds, do the spectra reported also show this muddy meta proton?
When in doubt, avoid the Stille coupling.

Offline Babcock_Hall

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Re: Reasons for amorphous peak in NMR?
« Reply #2 on: October 10, 2016, 05:34:25 PM »
One might consider the possibility of a paramagnetic impurity.  However, the hydrogen atoms closest to the paramagnetic center should show the greatest broadening, all else held equal.

Offline Irlanur

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Re: Reasons for amorphous peak in NMR?
« Reply #3 on: October 19, 2016, 04:55:18 AM »
can you post the spectrum/peak?

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