Search

A supramolecular approach based on self-assembled structures allows the formation of large structured co-assemblies based on chiral and achiral compounds with original physicochemical features. In this contribution, an achiral and hydrophobic porphyrin was co-assembled at the air-water interface with mesoscopic silica nano-helices dispersed in the water subphase of a Langmuir trough without covalent bond formation. This procedure allowed transferring the porphyrin/nano-helix co-assemblies on a solid support within a thin hybrid layer. The interaction between the two species was characterized using spectroscopic techniques and atomic force microscopy. As evidenced by the circular dichroism measurements performed directly on solid films, tunable chirality was induced to the porphyrin aggregates according to the chirality of the silica nano-helices. When the co-assemblies were transferred on surface plasmon resonance (SPR) slides and exposed to aqueous solutions of histidine enantiomers, selective chiral discrimination was observed which was determined by the matching/mismatching between the chirality of the analyte and the helicity of the nano-helical structure.

The possibility to employ carbon nanodots (CNDs) in solar devices was exploited by combining them with a fulleropyrrolidine derivative (FP2). The interaction between the two species was promoted by the presence of opposite electrostatic charges on CNDs (negatively charged) and FP2 (positively charged). The supramolecular dyad CNDs/FP2 generation was induced at the air/water interface of a Langmuir trough: water soluble CNDs were dissolved in the subphase and FP2 chloroform solution was spread on the subphase; the electrostatic interaction promoted the formation of the supramolecular adduct FP2/CNDs, which was then transferred onto solid substrates. Photo-induced charge transfer was promoted in the FP2/CNDs dyad and we demonstrated that the presence of CNDs increased the short-circuit current density, under light illumination, of a porphyrin-FP2/CNDs thin film by about 300% when compared with a more traditional porphyrin-FP2 solar device.