Method to improve resolution of two-dimensional heteronuclear correlation spectra in solid-state NMR
AssigneeBruker Analytik GmbH
InventorsLyndon Emsley, Dimitrios Sakellariou, Anne Lesage, Stefan Steuernagel
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AssigneeBruker Analytik GmbH
InventorsLyndon Emsley, Dimitrios Sakellariou, Anne Lesage, Stefan Steuernagel
Estimating the term…
A new two-dimensional NMR carbon-proton chemical shift correlation experiment, the MAS-J-HMQC experiment, is proposed for rotating solids. The magnetization transfer used to obtain the correlations is based on scalar heteronuclear J couplings. The 2D map provides through-bond chemical shift correlations between directly bonded proton carbon pairs in a similar way to corresponding high-resolution liquid state experiments. The transfer through J coupling is shown to be efficient and more selective that those based on heteronuclear dipolar couplings. The experiment, which works at high MAS spinning rates, yields the unambiguous assignment of the proton resonances. The experiment is demonstrated on several organic compounds.
A method of two-dimensional, heteronuclear correlation spectroscopy for the investigation of solid state samples, containing a first (1H) and a second (13C) nuclear species, in a nuclear magnetic resonance (NMR) spectrometer by means of an NMR pulse sequence, which pulse sequence comprises a preparation interval, an evolution interval, a mixing interval and a detection interval, wherein during the preparation interval the first nuclear species is excited by at least one preparation RF pulse in a first frequency band and is exposed to evolution RF pulses inside the first frequency band during the evolution interval and wherein during the detection interval the first nuclear species is exposed to at least one decoupling RF pulse inside the first frequency band while the free induction decay in the second frequency band is detected and wherein the pulse sequence (1≦p≦n) is repeated n times in a row with identical preparation interval, mixing interval and detection interval but with changed evolution interval and wherein the sample rotates with a rotation frequency greater than 1 kHz about an axis which is tilted by about 54° with respect to the axis of a homogeneous magnetic field and wherein the at least one preparation RF pulse is broad-banded with a center frequency in the center of the NMR spectrum of the first nuclear species of the sample effecting a rotation of the nuclear magnetization of the first nuclear species about an axis perpendicular to the direction of the magnetic field (X) with an angle of preferably 90° and wherein the evolution RF pulses form a so-called FSLG sequence with two successive broadband evolution RF pulses, phase shifted with respect to each other by 180° (Y, −Y), whose center frequencies are shifted in opposite directions with respect to the preparation RF pulse and which each effect a rotation of the nuclear magnetization of the first nuclear species by about 294°,
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