Among the interactions which govern NMR spectra, spin-spin coupling interactions provide the most direct form of structural information which is of interest to chemists. Dipolar coupling may be used to measure internuclear distances directly and J coupling may be used to identify bonding interactions and provide insights into the nature of the bonds. It is well known that the presence of a quadrupolar interaction reintroduces the dipolar interaction in spinning samples; however, similarly to the J coupling, this information is often lost if the observed nucleus is quadrupolar due to quadrupolar spectral broadening. Here we show for multiple spin pairs that double-rotation (DOR) NMR fully removes the effects of the quadrupolar interaction on the NMR spectrum leaving only the effects of dipolar and J couplings. We also demonstrate that the J coupling multiplets do not disappear for quadrupolar A2 spin pairs as they do for spin-1/2 nuclei. With DOR NMR, it is then straightforward to measure homonuclear J coupling constants between magnetically equivalent quadrupolar nuclei. A deeper understanding of the origins of the magnitudes and dominant mechanisms of J coupling for quadrupolar spin pairs in a series of related compounds is obtained by decomposing computed J coupling constants into their major molecular orbital contributions.
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7 May 2013
Research Article|
May 02 2013
Measuring dipolar and J coupling between quadrupolar nuclei using double-rotation NMR
Frédéric A. Perras;
Frédéric A. Perras
Department of Chemistry,
University of Ottawa
, Ottawa K1N 6N5, Canada
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David L. Bryce
David L. Bryce
a)
Department of Chemistry,
University of Ottawa
, Ottawa K1N 6N5, Canada
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a)
Author to whom correspondence should be addressed. Electronic mail: dbryce@uottawa.ca
J. Chem. Phys. 138, 174202 (2013)
Article history
Received:
February 15 2013
Accepted:
April 04 2013
Citation
Frédéric A. Perras, David L. Bryce; Measuring dipolar and J coupling between quadrupolar nuclei using double-rotation NMR. J. Chem. Phys. 7 May 2013; 138 (17): 174202. https://doi.org/10.1063/1.4802192
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