E. L. Diaz, Alexander A. Marchione, Jill E. Boyle
Nov 11, 2020
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Journal
Spectroscopy Letters
Abstract
Abstract A complete multinuclear magnetic resonance characterization of α,α-bis(4-fluorophenyl)-β-methyl-1H-imidazole-1-ethanol (a representative carbinoloimidazole topical anti-inflammatory agent) is presented, the first such assignment of a compound with diastereotopic fluorophenyl rings. The relative orientation of the 4-fluorophenyl rings was probed experimentally by 1H nuclear Overhauser effect spectroscopy experiments; these confirm the results of a density functional theory based optimization of the structure, in which the phenyl rings are oriented to avoid coplanarity. High resolution time-of-flight mass spectrometry confirmed the structure of the molecule.