Related Experiment Video
Updated: Mar 6, 2026

Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Unveiling One-Dimensional Supramolecular Structures Formed through π-π Stacking of Phenothiazines by Differential
Fernando R Carvalho1, Eduardo H Zampieri1, Wilker Caetano1
1Department of Chemstry, State University of Maringa, Av. Colombo 5790-CE, 87020-90, Maringá, Paraná, Brazil.
Abstract:
Organic-based nanomaterials can be self-assembled by strong and directional intermolecular forces such as π-π interactions. Experimental information about the stability, size, and geometry of the formed structures is very limited for species that easily aggregate, even at very low concentrations. Differential pulse voltammetry (DPV) can unveil the formation, growth, and also the stability window of ordered, one-dimensional, lamellar self-aggregates formed by supramolecular π stacking of phenothiazines at micromolar (10-6 mol L-1 ) concentrations. The self-diffusion features of the species at different concentrations are determined by DPV and used to probe the π staking process through the concept of the frictional resistance. It is observed that toluidine blue and methylene blue start to self-aggregate around 9 μmol L-1 , and that the self-aggregation process occurs by one-dimensional growth as the concentration of the phenothiazines is increased up to around 170 μmol L-1 for toluidine blue and 200 μmol L-1 for methylene blue. At higher concentrations, the aggregation process leads to structures with lower anisometry.
Related Concept Videos
Voltammetric Techniques: Pulse Voltammetry
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
π Electron Effects on Chemical Shift: Overview
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
¹H NMR: Complex Splitting
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied...

