Related Experiment Video
Updated: Jan 15, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Design and synthesis of macrocycles with tuneable diameters and helical foldamers with customizable peripheral side
Saquib Farooq1, Aurelien Crochet1, Andreas F M Kilbinger1
1Department of Chemistry, University of Fribourg Chemin du Musée 9 CH-1700 Fribourg Switzerland andreas.kilbinger@unifr.ch.
Abstract:
Tubular structures with nanosized pores have shown remarkable applications in areas such as ion transport and water filtration, but their development is often hindered by challenges including low yields, limited functionalization, and poor uniformity. Herein, we present a new series of macrocycles with tuneable diameters and helical foldamers featuring customizable peripheral side chains. The macrocycles, with diameters ranging from 0.8 to 1.4 nm, were synthesized in moderate to good yields using a one-pot method. Solid-state analysis revealed that these macrocycles form nanochannels, highlighting their potential applications in areas such as molecular recognition and artificial water channels (AWCs). Additionally, we synthesized helical aromatic amide polymers with narrow dispersities via a living chain-growth process. Our strategy enables the incorporation of diverse functional groups, including ethers, esters, acids, and amides, on the outer surfaces of the macrocycles or synthetic nanotubes. Circular dichroism (CD) spectroscopy confirmed the helical conformations of the polymers in solution. These macrocycles and foldamers present exciting opportunities for designing bioinspired membrane channels and functional nanotubes with tuneable hydrophobicity and cavity sizes, paving the way for innovative applications in nanotechnology and materials science.
More Related Videos
Related Concept Videos
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
Chair Conformation of Cyclohexane
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
Protein Folding
Conformations of Cycloalkanes

