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FDHALO17: The 15N NMR chemical shift in the characterization of weak halogen bonding in solution


We have studied the applicability of 15N NMR spectroscopy in the characterisation of the very weak halogen bonds of nonfluorinated halogen bond donors with a nitrogeneous Lewis base in solution. The ability of the technique to detect the relative strength of iodine-, bromine- and chlorine-centered halogen bonds, as well as solvent and substituent effects was evaluated. Whereas computations on the DFT level indicate that 15N NMR chemical shifts reflect the diamagnetic deshielding associated with the formation of a weak halogen bond, the experimentally observed chemical shift differences were on the edge of detectability due to the low molar fraction of halogen-bonded complexes in solution. The formation of the analogous yet stronger hydrogen bond of phenols have induced approximately ten times larger chemical shift changes, and could be detected and correlated to the electronic properties of substituents of the hydrogen bond donors. Overall, 15N NMR is shown to be a suitable tool for the characterisation of comparably strong secondary interactions in solution, but not sufficiently accurate for the detection of the formation of thermodynamically labile, weak halogen bonded complexes.

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Publication details

The article was received on 13 Mar 2017, accepted on 20 Mar 2017 and first published on 24 Mar 2017

Article type: Paper
DOI: 10.1039/C7FD00107J
Citation: Faraday Discuss., 2017, Accepted Manuscript
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    FDHALO17: The 15N NMR chemical shift in the characterization of weak halogen bonding in solution

    S. B. Hakkert, J. Gräfenstein and M. Erdelyi, Faraday Discuss., 2017, Accepted Manuscript , DOI: 10.1039/C7FD00107J

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