Abstract
IT is well known that the hydrogen bond gives rise in phenols to a large shift of the hydroxyl proton1–6. In a variety of compounds in which the OH groups are intermolecularly bonded, several workers have examined the chemical shifts of the hydroxyl proton in both the mono-meric and polymeric compound, through the signal frequency variation which follows dilution in solvents.
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References
Batdorf, R. L., Ph.D. thesis, Univ. Minnesota (1955).
Huggins, C. M., Pimentel, G. C., and Shoolery, J. N., J. Phys. Chem., 60, 1311 (1956).
Reeves, L. W., Allan, E. A., and Strømme, K. O., Canad. J. Chem., 38, 1249 (1960).
Porte, A. L., Gutowsky, H. S., and Hunsberger, I. M., J. Amer. Chem. Soc., 82, 5057 (1960).
Paterson, W. G., and Tipman, N. R., Canad. J. Chem., 40, 2122 (1962).
Allan, E. A., and Reeves, L. W., J. Phys. Chem., 66, 613 (1962).
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PALA, G. Proton Magnetic Resonance of the Hydrogen Bond in Phenols. Nature 204, 1190–1191 (1964). https://doi.org/10.1038/2041190a0
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DOI: https://doi.org/10.1038/2041190a0
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