IP Library Granted Patent US 7,746,071
Granted Patent B2
US 7,746,071 · App. 11/887,737 · Granted Jun 29, 2010

Method for the acquisition of data relating to multi-dimensional NMR spectra by means of frequency-dependent convolution

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Quick Facts
Patent No.
US 7,746,071
App. No.
11/887,737
Granted
Jun 29, 2010
Kind
B2
Abstract

In a method for the acquisition of data relating to multi-dimensional NMR spectra (designated as the SHARC protocol—SHaped, ARrayed aCquisition Protocol), crossed signals are shifted at will in frequency space using selective pulses and frequency dependent folding.

Claims (21)

1. A method for data acquisition of multi-dimensional NMR spectra with band-selective folding, the method comprising the steps of:

a) selecting n frequency ranges of chemical shifts for each arbitrary nuclear species whose correlation spectrum is to be detected; and

b) successively exciting the n frequency ranges, selected in step a), of the chemical shifts by suitable selective pulses, wherein n folded multi-dimensional NMR spectra are obtained per indirect dimension in a band-selective fashion and within one scanning process, which differ with respect to the respective degree of folding in the indirect spectral window.

2. The method of claim 1 , wherein, in step a), at least one frequency range is selected that contains overlapping, cross signals.

3. The method of claim 1 , wherein, in step a), a multi-dimensional NMR spectrum is acquired for selecting the frequency range.

4. The method of claim 3 , wherein the multi-dimensional NMR spectrum has low digital resolution.

5. A method for data acquisition of multi-dimensional NMR spectra with band-selective folding, the method comprising the steps of:

a) selecting n frequency ranges of chemical shifts for each arbitrary nuclear species whose correlation spectrum is to be detected; and

b) successively exciting the n frequency ranges, selected in step a), of the chemical shifts by suitable selective pulses, wherein n folded multi-dimensional NMR spectra are obtained per indirect dimension in a band-selective fashion and within one scanning process, which differ with respect to the respective degree of folding in the indirect spectral window, wherein, in step a), a multi-dimensional NMR spectrum is acquired with low digital resolution to determine the selected frequency range or frequency ranges are determined without acquiring an NMR spectrum with low digital resolution.

6. The method of claim 1 , wherein the multi-dimensional NMR spectrum is a homonuclear NMR spectrum, a heteronuclear NMR spectrum, or an imaging method.

7. The method of claim 1 , wherein the multi-dimensional NMR spectrum is a 2-dimensional or a 3-dimensional NMR spectrum.

8. The method of claim 1 , wherein the nuclear species is 1H, 13C or 15N.

9. The method of claim 1 , wherein the multi-dimensional NMR spectrum is a HSQC, HMBC, HMQC, COSY, DOSY, NOESY, ROESY, TOCSY or HSQC-TOCSY spectrum.

10. The method of claim 1 , wherein a T 1 /T 2 relaxation time is reduced.

11. The method of claim 1 , wherein, in step b), the pulse sequence and the incremented waiting times of the selective pulses correspond to the sequence shown in FIG. 1 .

12. The method of claim 1 , wherein, in step b), the pulses correspond to the pulse sequence shown in FIG. 6 or FIG.

13. The method of claim 1 , wherein, in step b), the pulses correspond to the pulse sequence shown in FIG. 7 or FIG. 7.1 .

14. The method of claim 1 , wherein steps a) and b) are performed simultaneously for more than only one nuclear species, wherein band-selective foldings are obtained in several indirectly measured spectral windows of respective nuclear species.

15. The method of claim 1 , further comprising calculating the chemical shifts of the corresponding non-folded multi-dimensional NMR spectrum from coordinates of cross signals of n folded indirect spectral windows.

16. Use of the method of claim 1 , for facilitating evaluation of multi-dimensional NMR spectra.

17. Use of the method of claim 1 , for analyzing structure of inorganic and organic compounds, for analyzing structure of natural substances and/or peptides, for automatic structure determination, for biological NMR spectroscopy, for screening of organic compounds, for analysis of complex mineral oil fractions, or in metabonomics.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 17, 2024
From: BRUKER BIOSPIN GMBH
To: BRUKER BIOSPIN GMBH & CO. KG
Reel/Frame 067767/0336 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2007
From: SAKHAII, PEYMAN
To: BRUKER BIOSPIN GMBH
Reel/Frame 019976/0901 →