Hydrogen Bonding within Dynamic 19 F-Tagged Oligothiourea Foldamers in Solution and in Membranes
Year: 2026
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Molecular conformation plays an integral role in biological signal transduction, with several classes of biomolecules using conformational changes to translate local inputs into spatially remote outputs. This natural communication mechanism has inspired the development of dynamic foldamers with the ability to use conformational changes as a communication mechanism. These foldamers include ethylene-bridged hydrogen-bonded oligo(thio)urea foldamers with reversible hydrogen-bond polarity. Using p -fluorobenzyl capping groups, we show that 1 H and 19 F variable-temperature and 2D NMR reveal details of the directionality and resilience of the intramolecular hydrogen-bond network of these dynamic foldamers at a range of temperatures. Crucially, 19 F VT NMR allowed the dynamic behavior of the foldamers to be studied in micelles and bicelles, into which they were readily incorporated. The intactness of the network was investigated both in solution and in membrane-mimetic environments by 19 F NMR spectroscopy for foldamers containing between two and five thioureas. With longer foldamers, the high resolution and sensitivity of the fluorine probes allowed intermediates in the global hydrogen-bond directionality reversal process to be identified. These findings reveal subtleties in the conformational preferences of hydrogen-bonded foldamers that have relevance to their use as communication devices both in solution and in membranes separating compartmentalized environments.
DOI: 10.1021/jacs.6c05314
Institution: University of Bristol
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W7164998644