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Attempts to use NMR techniques to understand the rates of isomerization and possibly to determine the activation parameters were unsuccessful. Proton NMR of (±)-3 in CDCl3, DMSO-d6, and CD3OD in the presence of d-trifluoromethylphenylcarbinol as a chiral solvent did not display differences in the chemical shifts of the two atropisomers. Proton-decoupled 19F NMRs were also run under the above three conditions. CDCl3 was the only solvent in which the two atropisomers showed different signals at δ -62.32 and -62.34 ∼8.5 Hz separation, However, the sample could not be heated beyond 60° C in this solvent due to limitations related to the instrumentation. Below 60 °C no interconversion of the atropisomers was observed
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3 was the only solvent in which the two atropisomers showed different signals at δ -62.32 and -62.34 (∼8.5 Hz separation). However, the sample could not be heated beyond 60° C in this solvent due to limitations related to the instrumentation. Below 60 °C no interconversion of the atropisomers was observed.
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