ABSTRACT
Here, we study organogels prepared thanks to a new organogelator, the N-oleyldiamide molecule, which shows a remarkable propensity to gelify a large scope of solvents, from aprotic to high protic solvents. The solvent plays a key role in the formation and stability of supramolecular self-assemblies. However, the understanding and the control of its effects can be complex as many parameters are a priori involved. This study aims to understand the effect of solvent on the structures of organogels and on their final mechanical properties. Five solvent classes have been selected ranking from low protic to high protic, according to the Hansen H-bond parameter δh. The solvent proticity appears to be one of the main parameters that affect the organogel internal structure and therefore the final rheological properties. For a given organogelator fraction, the terminal elastic modulus measured by oscillatory rheology is observed to increase significantly with the Hansen H-bond solvent parameter δh. Materials of different mechanical properties are then shown to display various structures, which are investigated thanks to cryo-SEM. Besides, wide-angle X-ray scattering (WAXS) has been used to probe the gelator organization at the molecular scale with regard to the solvent nature, to understand the supramolecular self-assembly of this promising molecule.
