Constant-time 2D and 3D through-bond correlation NMR spectroscopy of solids under 60 kHz MAS
Creators
- 1. Biophysics and Department of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109-1055 (United States)
Description
Establishing connectivity and proximity of nuclei is an important step in elucidating the structure and dynamics of molecules in solids using magic angle spinning (MAS) NMR spectroscopy. Although recent studies have successfully demonstrated the feasibility of proton-detected multidimensional solid-state NMR experiments under ultrafast-MAS frequencies and obtaining high-resolution spectral lines of protons, assignment of proton resonances is a major challenge. In this study, we first re-visit and demonstrate the feasibility of 2D constant-time uniform-sign cross-peak correlation (CTUC-COSY) NMR experiment on rigid solids under ultrafast-MAS conditions, where the sensitivity of the experiment is enhanced by the reduced spin-spin relaxation rate and the use of low radio-frequency power for heteronuclear decoupling during the evolution intervals of the pulse sequence. In addition, we experimentally demonstrate the performance of a proton-detected pulse sequence to obtain a 3D 1H/13C/1H chemical shift correlation spectrum by incorporating an additional cross-polarization period in the CTUC-COSY pulse sequence to enable proton chemical shift evolution and proton detection in the incrementable t1 and t3 periods, respectively. In addition to through-space and through-bond 13C/1H and 13C/13C chemical shift correlations, the 3D 1H/13C/1H experiment also provides a COSY-type 1H/1H chemical shift correlation spectrum, where only the chemical shifts of those protons, which are bonded to two neighboring carbons, are correlated. By extracting 2D F1/F3 slices (1H/1H chemical shift correlation spectrum) at different 13C chemical shift frequencies from the 3D 1H/13C/1H spectrum, resonances of proton atoms located close to a specific carbon atom can be identified. Overall, the through-bond and through-space homonuclear/heteronuclear proximities determined from the 3D 1H/13C/1H experiment would be useful to study the structure and dynamics of a variety of chemical and biological solids
Additional details
Identifiers
- DOI
- 10.1063/1.4940029;
Publishing Information
- Journal Title
- Journal of Chemical Physics
- Journal Volume
- 144
- Journal Issue
- 3
- Journal Page Range
- p. 034202-034202.8
- ISSN
- 0021-9606
- CODEN
- JCPSA6
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47063796
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; ATOMS; CARBON; CARBON 13; CHEMICAL SHIFT; CORRELATIONS; COSY STORAGE RING; DECOUPLING; HYDROGEN 1; KHZ RANGE; MOLECULES; NMR SPECTRA; NUCLEAR MAGNETIC RESONANCE; POLARIZATION; PROTON DETECTION; PROTONS; RADIOWAVE RADIATION; SOLIDS; SPIN-SPIN RELAXATION
- Descriptors DEC
- ACCELERATORS; BARYONS; CARBON ISOTOPES; CHARGED PARTICLE DETECTION; CYCLIC ACCELERATORS; DETECTION; ELECTROMAGNETIC RADIATION; ELEMENTARY PARTICLES; ELEMENTS; EVEN-ODD NUCLEI; FERMIONS; FREQUENCY RANGE; HADRONS; HYDROGEN ISOTOPES; ISOTOPES; LIGHT NUCLEI; MAGNETIC RESONANCE; NONMETALS; NUCLEI; NUCLEONS; ODD-EVEN NUCLEI; RADIATION DETECTION; RADIATIONS; RELAXATION; RESONANCE; SPECTRA; SPECTROSCOPY; STABLE ISOTOPES; STORAGE RINGS; SYNCHROTRONS
Optional Information
- Notes
- (c) 2016 AIP Publishing LLC