Stimuli-Responsive Properties of Supramolecular Gels Based on Pyridyl-N-oxide Amides.
Ontology highlight
ABSTRACT: The nature of functional groups and their relative position and orientation play an important role in tuning the gelation properties of stimuli-responsive supramolecular gels. In this work, we synthesized and characterized mono-/bis-pyridyl-N-oxide compounds of N-(4-pyridyl)nicotinamide (L1-L3). The gelation properties of these N-oxide compounds were compared with the reported isomeric counterpart mono-/bis-pyridyl-N-oxide compounds of N-(4-pyridyl)isonicotinamide. Hydrogels obtained with L1 and L3 were thermally and mechanically more stable than the corresponding isomeric counterparts. The surface morphology of the xerogels of di-N-oxides (L3 and diNO)
SUBMITTER: Jayabhavan SS
PROVIDER: S-EPMC9956205 | biostudies-literature | 2023 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA