| Autor: |
Poole WG; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Peron F; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Fox SJ; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Wells N; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Skylaris CK; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Essex JW; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Kuprov I; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K., Linclau B; School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K.; Department of Organic and Macromolecular Chemistry, Ghent University, Krijgslaan 281-S4, 9000 Ghent, Belgium. |
| Abstrakt: |
Fluorine substitution can have a profound impact on molecular conformation. Here, we present a detailed conformational analysis of how the 1,3-difluoropropylene motif (-CHF-CH 2 -CHF-) determines the conformational profiles of 1,3-difluoropropane, anti - and syn -2,4-difluoropentane, and anti - and syn -3,5-difluoroheptane. It is shown that the 1,3-difluoropropylene motif strongly influences alkane chain conformation, with a significant dependence on the polarity of the medium. The conformational effect of 1,3-fluorination is magnified upon chain extension, which contrasts with vicinal difluorination. Experimental evidence was obtained from NMR analysis, where polynomial complexity scaling simulation algorithms were necessary to enable J -coupling extraction from the strong second-order spectra, particularly for the large 16-spin systems of the difluorinated heptanes. These results improve our understanding of the conformational control toolkit for aliphatic chains, yield simple rules for conformation population analysis, and demonstrate quantum mechanical time-domain NMR simulations for liquid state systems with large numbers of strongly coupled spins. |
