Reversible J- to H-aggregate transformation in thin films of a perylenebisimide organogelatorElectronic supplementary information (ESI) available. See DOI: 10.1039/c4tc02444c

A perylene bisimide organogelator is shown to behave as a reversible stimuli responsive material: thermal annealing and contact with organic non solvents allow to switch back and forth between a green J-type (Form I) and a red H-type (Form II) aggregate in thin films and powders of a N , N ′-substituted H-bonding perylenebisimide (PBI-C10). Both, Form I and II were characterized by transmission electron (low dose high-resolution and electron diffraction) and atomic force microscopies, UV-vis and FTIR spectroscopies. The Form I → Form II transformation implies a redistribution of inter-molecular H-bonds between PBI molecules that form columnar stacks in Form I and supramolecular helices with enhanced long-range stacking in Form II. The reverse transformation is triggered by a contact of Form II films with H-bonding organic non solvents e.g. linear alcohols. It is proposed that solvent molecules diffusing in the Form II films can disrupt long-range H-bonding within helical stacks of Form II. Accordingly, PBI-C10 is shown to behave as a functional material responding successively to thermal and molecular stimuli. A perylene bisimide organogelator is shown to behave as a reversible stimuli responsive material: thermal annealing and contact with organic non solvents allow to switch back and forth between a green J-type (Form I) and a red H-type (Form II) aggregate in thin films and powders of a N , N ′-substituted H-bonding perylenebisimide (PBI-C10).