This invention is associated with NMR multi-dimensional spectroscopy. It is an NMR multi-dimensional spectroscopy for measuring 1H—1H coupling values within several coupling networks.
Spin-spin coupling, an important parameter in NMR spectroscopy, plays an important role in molecular structure analysis. Among various scalar couplings, the three-bond 1H—1H coupling, whose magnitude is dependent on the dihedral angle between the two C—H vectors, is widely used in molecular conformational study. However, the measurement of 1H—1H coupling constants is often hampered by small chemical-shift dispersion and complex splitting patterns. A PSYCHEDELIC method was proposed by Davy Sinnaeve et al. for revealing the scalar coupling network of a selected proton and measuring relevant coupling constants, greatly facilitating the measurement of J values (D. Sinnaeve, M. Foroozandeh, M. Nilsson, G. A. Morris, A general method for extracting individual coupling constants from crowded 1H NMR spectra, Angew. Chem. Int. Ed. 55 (2016) 1090-1093.). However, this method can analyze only one coupling networks at a time. Several experiments are needed for revealing all coupling networks.
This invention is aimed at providing a simple and convenient NMR spectroscopy for simultaneously revealing several scalar coupling networks and extracting all coupling constants within them.
In order to solve the technical problem mentioned above, this invention provides an NMR multi-dimensional method for measuring coupling constants within several coupling networks, and the main steps are as below:
The PSYCHE element mentioned above includes two chirp pulses with small flip angle and opposite sweeping directions, and a simultaneously applied gradient G2. The PSYCHE element is flanked by two spoiling gradients Gs.
The EPSI readout mentioned above includes oscillating gradients Ga and −Ga, and simultaneous samplings, of which the duration under one gradient is Ta.
The number of the increments (ni) should be set according to the required digital resolution in the indirect dimension: ni=SW1/ν1, where ν1 is the digital resolution in the indirect dimension and SW1 is the spectral width in the indirect dimension.
The number of loops of the acquisition windows (N) should be set according to the required digital resolution in the direct dimension: N=SW1D/ν2, where ν2 is the digital resolution in the direct dimension.
The flip angle of the chirp pulses (β) is chosen for the balance between signal-to-noise ratio (SNR) and spectral purity. Larger β results in higher SNR, but leads to stronger artifacts. In general, β can be set as 15°˜20°.
This invention provides an NMR multi-dimensional method for measuring coupling constants within several coupling networks. After the excitation of the 90° hard pulse, in the middle of the evolution time t1, a selective 180° pulse and a gradient are implemented simultaneously, then two chirp pulses with low flip angle and opposite sweeping direction is implemented at the presence of another gradient. The two chirp pulses are flanked by a pair of spoiling gradient for the selection of coherence transfer pathway. After the gradient Gp, the EPSI readout is used to record NMR signals. Several scalar networks can be revealed through our experiment, with relevant coupling constants extracted.
Now we combine the figures and a practical example to further explain our invention.
This invention provides an NMR multi-dimensional method for measuring coupling constants within several coupling networks, and the main steps are as below:
After disentangling different signals, relevant J coupling constants can be measured.
The PSYCHE element mentioned above includes two chirp pulses with small flip angle and opposite sweeping directions, and a simultaneously applied gradient G2. The PSYCHE element is flanked by two spoiling gradients Gs.
The EPSI readout mentioned above includes oscillating gradients Ga and −Ga, and simultaneous samplings, of which the duration under one gradient is Ta.
The number of the increments (ni) should be set according to the required digital resolution in the indirect dimension: ni=SW1/ν1, where ν1 is the digital resolution in the indirect dimension and SW1 is the spectral width in the indirect dimension.
The number of loops of the acquisition windows (N) should be set according to the required digital resolution in the direct dimension: N=SW1D/ν2, where ν2 is the digital resolution in the direct dimension.
The flip angle of the chirp pulses (β) is chosen for the balance between signal-to-noise ratio (SNR) and spectral purity. Larger β results in higher SNR, but leads to stronger artifacts. In general, β can be set to 15°˜20°.
According to the method described above, the practical operation is as below:
This example was performed on an 11.7 T (proton resonance frequency of 500 MHz) Agilent NMR System (Agilent Technologies, Santa Clara, Calif., USA) with a 54 mm narrow bore equipped with a z field gradient, using a sample of 1 M/L n-butyl bromide in CDCl3. The pulse sequence in
After the experiment, for each t1, we extracted the data recorded under positive gradients and arranged them to a 2D matrix. Thus a 3D dataset was obtained and then processed by a 3D Fourier transformation. After extracting 2D spectra of relevant slices, 2D spectra respectively corresponding to scalar coupling networks of the three protons were obtained. Then relevant J coupling constants could be measured.
The spectrum in
The spectrum in
The spectrum in
In conclusion, this invention provides a NMR multi-dimensional method for measuring coupling constants within several coupling networks. It is simple and efficient, and will find extensive applications in molecular structure elucidation.
The example described above is only a superior implementation of this invention. Therefore, the application of this invention is not limited to this example, that is, all modifications and alterations of this invention according to this invention specification is covered by the claim of this invention.
This invention provides a NMR multi-dimensional method for measuring coupling constants within several coupling networks. After the excitation of the 90° hard pulse, in the middle of the evolution time t1, a selective 180° pulse and a gradient are implemented simultaneously, then two chirp pulses with low flip angle and opposite sweeping direction is implemented at the presence of another gradient. The two chirp pulses are flanked by a pair of spoiling gradient for the selection of coherence transfer pathway. After the gradient Gp, the EPSI readout is used to record NMR signals. Several scalar networks can be revealed through our experiment, with relevant coupling constants extracted. This method is simple and efficient and will find extensive applications in molecular structure elucidation.
Number | Date | Country | Kind |
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201710025922.1 | Jan 2017 | CN | national |
Filing Document | Filing Date | Country | Kind |
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PCT/CN2018/071808 | 1/8/2018 | WO | 00 |