Adelino Marques MendesPaulo Ernesto Antonelli
The incorporation of a hexadecyl group on imidazolium, pyridinium, and pyrrolidinium scaffolds produces low-molecular-weight ionic organogelators that can gel several types of ionic liquids, deep eutectic solvents (DESs), and several molecular organic solvents. Minimum gelator concentrations fall in the 0.9-15.0% (w/v) range, with the lower end of the gelator concentrations observed in the gelation of DESs. On the basis of polarized optical microscopy, differential scanning calorimetry, and X-ray data, crystallization of these salts appear to produce high-surface-area crystals, which generate sufficiently stable three-dimensional networks that are capable of trapping the solvent molecules. Importantly, the nature of the fluid component of the gel appears to have a profound effect on the morphology of the crystallized organogelators. On the other hand, the organogelators appeared to modulate phase transitions of the liquids.
Christianne de Faria Coelho‐RavagnaniPaula Fabrício SandreschiThiago Silva PiolaLeandro dos SantosDaniela Lopes dos SantosGiovana Zarpellon MazoJoilson MeneguciMarília de Almeida CorreiaTânia Rosane Bertoldo BenedettiAntônio Henrique Germano-SoaresPedro Curi HallalEdílson Serpeloni Cyrino
Mauricio RamosLeonéa Vitória Santiago
Ana Laura Oliveira Freitas Gorosthides de MouraKamila Ribeiro PeixotoRenata Dantas Queiroz CaetanoNaianne de Paula NascimentoMariana de Sousa Nunes VieiraHeloísa Silva Guerra
Giovana Zarpellon MazoTânia Bertoldo Benedetti