Hi Edward,

Thank you so much, again.

I guess I will start calibrating temperature before my experiments from now on!
One precision, I always use temperature compensation blocks as well as 
interleaving (in the sense of indirect dimension increment interleaving in a 
pseudo-3D).

However I am a bit confused now by what you mean with "single scan", "single 
fid" and "single experiment" interleaving? Would you comment on this?

Best regards,
Thibault

On 4/18/19, 11:09 AM, "Edward d'Auvergne" <[email protected]> wrote:

            External Email - Use Caution        
    
    On Tue, 16 Apr 2019 at 23:57, Viennet, Thibault
    <[email protected]> wrote:
    > Hi Edward,
    >
    > Thank you so much for your previous answer, it has been very helpful to 
interpret my data.
    > If I may I will bother you with another question though.
    >
    > I run consistency testing for model free analysis and even if does not 
look bad (around 1.06 in my case) I was wondering if there is a way to correct 
for this without going back to acquire data, checking temperature calibration, 
etc.
    > Maybe there is an empirical way? Changing the field strength used by 
Relax by a correction factor?
    >
    > What are your thoughts about this?
    
    Hi,
    
    There are zero empirical ways to fix bad data, if that is what you
    really have.  What you can do is book say 2 hours on the spectrometer
    and run mini-versions of the experiments on methanol/ethylene glycol
    and determine the exact temperature from the spectra.  If the
    temperature differences between all 3 experiments is < 0.5 degrees,
    you should be fine.  Note that if the experiments are not interleaved
    in any way (scan or fid interleaving), you will have the daily
    temperature fluctuations of the NMR hall mixed into your data.  That
    effect is quite bad.
    
    If the temperature is significantly different between experiments (>
    0.5 deg), then you cannot use the data.  Or at least no one will trust
    your results and hence conclusions.  The reason is because the
    dynamics of the molecule changes non-linearly with temperature.  The
    most important factor is the impact it has on the Brownian diffusion
    of the molecules in the NMR tube.  With > 0.5 deg, the global
    diffusion tensor will be significantly different between the
    experiments and hence you cannot use the one tensor for all input
    data.  There is no theory in existence to deal with this.
    
    So you really need to carefully determine if your data is 'good' or
    'bad'.  If bad, remeasurement is unfortunately the only solution.
    However you should note that almost everyone remeasures at least once
    or twice when measuring relaxation data for the first time.  NMR
    spectroscopists with relaxation experience will also sometimes have to
    remeasure bad data.
    
    Regards,
    
    Edward
    



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