Using combined dielectric and light-scattering measurements, the authors show that all three phenyl-propanol isomers, including 1-phenyl-1-propanol, retain a Debye-like dielectric relaxation, indicating hydrogen-bonded chain or ring structures are not fully suppressed by steric hindrance.
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The Influence of Molecular Architecture on the Dynamics of H-Bonded Supramolecular Structures in Phenyl-Propanols
Using combined dielectric and light-scattering measurements, the authors show that all three phenyl-propanol isomers, including 1-phenyl-1-propanol, retain a Debye-like dielectric relaxation, indicating hydrogen-bonded chain or ring structures are not fully suppressed by steric hindrance.