Conformational preference in difluoroacetamide oligomers: probing the potential for foldamers with C–H?O hydrogen bonds?
Organic & Biomolecular Chemistry Pub Date: 2023-06-27 DOI: 10.1039/D3OB00811H
Abstract
The C–H bond of a difluoroacetamide group, acidified by two adjacent fluorine atoms, could in principle provide conformational organisation for foldamers based on C–H?O hydrogen bonds. We find that in model oligomeric systems, this weak hydrogen bond leads only to partial organisation of the secondary structure, with the conformational preference of the difluoroacetamide groups being predominantly governed by dipole stabilisation.
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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