The supramolecular aggregation of three diimidazolium-functionalized perylene bisimides, differing in thealkyl chain length was investigated. These salts form aggregatesin solvents like chloroform, dichloromethane, and glycerol.Solvent-, concentration-, and temperature-dependentspectroscopic studies were carried out, evidencing the occurrenceof an isodesmic, enthalpy-driven aggregation process,underpinned by p–p stacking and hydrogen bonding.Moreover, dynamic light scattering (DLS) measurements andSEM images revealed that these salts aggregate in chloroforminto elongated structures.
|Numero di pagine||11|
|Rivista||CHEMISTRY-A EUROPEAN JOURNAL|
|Stato di pubblicazione||Published - 2015|
All Science Journal Classification (ASJC) codes
- Organic Chemistry