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Chemical shifts of phenolic monomers in solution and implications for addition and self‐condensation
Author(s) -
Haupt Robert A.,
Renneckar Scott
Publication year - 2013
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.3914
Subject(s) - chemistry , chemical shift , ionic bonding , alkali metal , solvent effects , inorganic chemistry , condensation reaction , solvent , computational chemistry , ion , organic chemistry , catalysis
Alkali metal counter‐cations alter the electron density of phenolates in solution by electrostatic interactions. This change in electron density affects their reactivity toward formaldehyde, hydroxymethylphenols, and isocyanates during polymerization. The electronic perturbation of phenolic model compounds in the presence of alkali metal hydroxides was investigated with 13 C and 1 H nuclear magnetic resonance in polar solvents relative to non‐ionic controls, altering the chemical shifts of the model compounds, thus indicating changes in electron density using the chemical shift as a proxy. These shifts were attributed to Coulombic electrostatic interactions of the counter‐cation with the phenolate anion that correlated to hydrated ionic radius and solvent dielectric constants. The predicted relative reaction rates for formaldehyde addition based on electron density ranking from 13 C nuclear magnetic resonance of the phenolic models was compared with the literature values. Predictions for condensation reactions of 2‐ and 4‐hydroxymethylphenol from chemical shifts were consistent with published results. The results permit predictions for the reaction of phenolic compounds for the formation of thermosetting polymeric materials. Copyright © 2012 John Wiley & Sons, Ltd.