morsagh
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NMR reading
Please, what is the best freeware program (for windows XP) for reading NMR output files. I have this file (in attachment) but i don´t know how to
open it to see my spectrum. Or can somebody just open it in correct software and send me screens of my spectrum? Thank you very much
Attachment: fid (256kB)
This file has been downloaded 1217 times
[Edited on 1-3-2016 by morsagh]
[Edited on 1-3-2016 by morsagh]
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Metacelsus
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ACD labs used to have good NMR freeware, but they recently discontinued it.
When I try opening it in MNova, your file gives an "unknown format of file" error (it might be the file, or it might be that MNova has a problem).
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UC235
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I think spinworks will open it and it's free. The program is half-broken. It can't output any sort of normal file format so you have to paste the
spectra into a word document or similar to save them.
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morsagh
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Spinworks didn´t work. Can´t somebody open it and make printscreens because i realy don´t know what to do.
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aga
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What was the full name of the file, including the extension i.e. fid.fid, fid.raw etc ?
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Nicodem
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You need all the FID data, not just a single file. It should be a folder full of files.
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Metacelsus
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Yes, Nicodem's right (that's why MNova was giving me the error, now that I think about it). If you can post the folder, I can send you the spectrum
(and maybe even try to interpret it).
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Heavy Walter
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Sure it is a NMR data and not a FID (GC) data?
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morsagh
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Hi again, I have now printscreens of my spectrum. It should be camphor after reduction, so mixture of camphor and very little of borneol or
isoborneol. I need to know if there is some borneol or isoborneol and my reduction was successful (it can be very low yield) but spectrum is quite
complicated for me. If you help I would be very happy...
  
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UC235
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Go to http://sdbs.db.aist.go.jp/ and look up borneol, isoborneol, and camphor. They have NMR spectrums for all (albeit on a low powered machine) and
peak assignments. You can probably find better ones elsewhere, but it is conveniently in one place.
You'll note that the peaks at 3.6 and 4 are specific to isoborneol and borneol and are the alpha-proton to the alcohol group. Given the intensity of
the peaks, I don't think there is very much of them, but they are present. The significant peak at 2.36 is camphor's exo-proton on the carbon adjacent
to the ketone group. In borneol and isoborneol it is more shielded and appears 0.1ppm upfield at 2.26ppm.
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aga
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How ? Was that file you uploaded a compressed archive or what ?
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morsagh
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So this peaks are isoborneol and borneol you think?
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morsagh
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I just asked Mrs from lab to send me printscreens, so i don´t know where was problem.
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UC235
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I think the 4 peaks on the left are all a quartet of godknowswhatets mixed with baseline noise
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aga
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Please ask Mrs to tell you what the problem was, then post the solution here.
The next person asking the same as you did might get a faster solution to the same problem.
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morsagh
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I'll ask aga. So you UC235 think that borneol is in my sample? Did i marked correct peaks? I want to compare integrals to know yield, so it will be
good to know which are hydrogen on alpha to alcohol.
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