*(sin(x) /x) (*or

*sinc(x))*functions. The

*sinc(x)*function has a large central lobe with satellite lobes of alternating positive and negative sign. In order to obtain uniform excitation and therefore quantitative data, one must ensure that the excitation pulse is sufficiently short to allow the entire spectral width of interest to fit within a small region of the central

*sinc(x)*lobe. The pulse must also have sufficient amplitude to produce a 90° rotation of the magnetization. The excitation profile of four pulses is shown in the figure below.The data were obtained by measuring a 300 MHz

^{1}H NMR spectrum of HDO as a function of transmitter frequency. The power level for each of the pulses was set such that the pulses provided a 90° flip angle for an on-resonance signal. Each spectrum was phased independently. The first zero crossings of the

*sinc(x)*function are at + 1/(PW) and -1/(PW) where PW is the duration of the pulse. It is therefore important that the spectral width of interest be less than ~1/(10PW) to ensure uniform excitation. One can see that a 10 µsec pulse provides essentially flat excitation across 40 kHz whereas 50, 100 and 200 µsec pulses do not.

## 8 comments:

Hi,

If one is dealing quadrupolar nuclei (say 1st order), how would one pick pulse lengths so that the central transition and satellites are uniformly excited? I have read that for large quadrupolar interactions, that the ratio of omega(rf)/omega(Q) is linear for the central transition if the pulse lengths are short. It isn't linear though for the satellites. How would one pick the best pulse lengths? Any advice? Thanks.

Maggie

Can you recommend a good book that discusses this?

Maggie,

Often it is simply impossible to uniformly excite the satellite transitions as the quadrupolar coupling is too large. The breadth of the spectrum exceeds the bandwith of the probe. In such cases, spectra are recorded in "chunks" using the QCPMG technique to get the lineshape.

Glenn

Anonymous,

Excitation profiles are discussed in Neil Jacobsen's book "NMR Spectroscopy Explained"

Glenn

When looking at wideline spectra is it possible to set an output power so high that when looking at the FID or spectra that more than one peaks appears? I am guessing this would be due to the difference in the nutation frequencies?

maggie

Maggie,

I'm not sure I understand your question. Are you asking whether or not one can see more than one isotope in a spectrum? If so, the answer is yes. See this link:

http://u-of-o-nmr-facility.blogspot.com/2008/05/simultaneous-nmr-of-both-23-na-and-51-v.html

Glenn

Actually, I wasn't wondering about seeing another isotope. A while back, I was trying to find the 90 deg time for a sample (quadrupole - wideline)and saw that at larger pulse widths, there were 2 peaks rather than 1 at shorter pulse lengths. I was doing this at pretty high power, so I thought that this was the issue. I don't know if this makes sense or not.

The original post stated that the zero crossings of the excitation profile occur at plus and minus 1/(2PW). This was based on information in Neil Jacobsen's book, NMR Spectroscopy Explained (pp. 297-299). This disagrees with the information given in a book by Kenneth MacKenzie and M.E. Smith, Multinuclear Solid State NMR of Inorganic Materials (pp. 111-112) which state that the zero crossings are at 1/PW and not 1/(2PW). The latter agrees best with the data presented here and the original post was corrected. Thank you to Victor Terskikh for pointing this out. He explained the discrepency as follows, "The confusion seems to originate in the matter how the pulse is represented in sinc: if the pulse is -pw/2 to pw/2 (around zero), then the FT gives zero excitation at 1/pw. If the pulse is presented as from 0 to pw*, then FT gives a crossing at 1/2pw*. But in NMR the first case applies, while the second case is just the half of the real pulse pw*=pw/2"

Glenn

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