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Chemical shift correlation spectroscopy in rotating solids: Radio frequency-driven dipolar recoupling and longitudinal exchange

Bennett, A. E., Griffin, R. G., Ok, J. H., Vega, S.·1992·The Journal of Chemical Physics

Abstract

We present a new method of performing chemical shift correlation spectroscopy in solids with magic angle spinning (MAS). Its key feature is a longitudinal mixing period of π pulses that recouples the dipolar interaction. We discuss experimental results for triply-13C-labeled alanine and a theory combining MAS and π pulses.

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Metadata

Authors
Bennett, A. E., Griffin, R. G., Ok, J. H., & Vega, S.
Venue
The Journal of Chemical Physics
Published
1992-06-01
Volume
96
Issue
11
Pages
8624-8627
ISSN
  • 0021-9606 (ISSN-L)
  • 1089-7690
OpenAlex
W1968779811
Cited by
671
References
0
FWCI
15.05
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Chemical shift correlation spectroscopy in rotating solids: Radio frequency-driven dipolar recoupling and longitudinal exchange. https://app.cochat.ai/papers/10.1063/1.462267
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Bennett, A. E., Griffin, R. G., Ok, J. H., & Vega, S. (1992). Chemical shift correlation spectroscopy in rotating solids: Radio frequency-driven dipolar recoupling and longitudinal exchange. The Journal of Chemical Physics. https://doi.org/10.1063/1.462267

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.