DOSY Experiments - Emory University
DOSY Experiments - Emory University
DOSY Experiments - Emory University
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gt1 total length of the phase encoding gradient<br />
gzlvl1 strength of the phase encoding gradient<br />
pp 90 deg. hard 1 H pulse<br />
pplvl decoupler power level for pp pulses<br />
sspul flag for a GRD-90-GRD homospoil block<br />
gzlvlhs gradient level for sspul<br />
hsgt gradient duration for sspul<br />
sspulX<br />
flag for a GRD-90-GRD homospoil block during del to destroy<br />
original X magnetization (using hsgt and gzlvlhs)<br />
j1xh one-bond X-H coupling<br />
mult<br />
multiplicity;<br />
1 selects CH's (doublets);<br />
1.5 gives CH2's down, CH's and CH3's up;<br />
0.5 enhances all protonated carbons<br />
alt_grd flag to invert gradient sign on alternate scans (default = 'n')<br />
lkgate_flg flag to gate the lock sampling off during gradient pulses<br />
probe_ stores the probe name used to acquire the dosy experiment<br />
Processing Parameters:<br />
determines the number of components to be used in fitting the<br />
ncomp<br />
signal decay in <strong>DOSY</strong> when dosyproc='discrete'.<br />
nugflag<br />
nugcal_[1-5]<br />
dosyproc<br />
dosybypoints<br />
'n' uses simple mono- or multi-exponential fitting to estimate<br />
diffusion coefficients<br />
'y' uses a modified Stejskal-Tanner equation in which the exponent<br />
is replaced by a power series.<br />
a 5-membered parameter array summarizing the results of the<br />
calibration of non-uniform field gradients. Used if nugflag='y',<br />
requires a preliminary NUG-calibration by the Doneshot_nugmap<br />
sequence. The values are taken from the probe file at the time of<br />
the data acquisition<br />
'discrete' - invokes monoexponential fitting with dosyfit if ncomp=1,<br />
and multiexponential fitting with the external programme SPLMOD<br />
if ncomp>1.<br />
'continuous' invokes processing with the external programme<br />
CONTIN and gives a continuous distribution in the diffusion<br />
domain.<br />
'n' divides the spectrum into individual peaks, creating one crosspeak<br />
for each individual peak found in the 1D spectrum 'y' performs<br />
a diffusion fit for every point in the displayed region of the spectrum<br />
that lies above the selected threshold.<br />
This sequence uses the higher “resolving power” of the wide 13 C chemical shift range, while the<br />
phase encoding and decoding step is done more effectively on the 1 H magnetization.<br />
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