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.