Related Experiment Video
Updated: Jan 13, 2026

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications
Published on: August 28, 2015
Tripartite hydrogen-bonding as a driving force for high-concentration cyclization of poly(l-lactide)
Sébastien Moins1, Alexandre Mignot2, Céline Henoumont3
1Laboratory of Polymeric and Composite Materials, University of Mons Place du Parc 23 7000 Mons Belgium olivier.coulembier@umons.ac.be.
Abstract:
A three-step strategy enables efficient cyclization of high-M n PLLA at 0.5 M. Key to success is a persistent tripartite complex driven by hydrogen bonding and ion pairing. Selective intramolecular transesterification at a benzylic ester triggers ring closure, affording cyclic PLLA (M n ≈ 26 000 g mol-1) under synthetically practical conditions. SPM imaging reveals nanorings with diameters consistent with the expected contour length of cyclic PLLA chains.
More Related Videos
11:42Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
06:56Characterization of Synthetic Polymers via Matrix Assisted Laser Desorption Ionization Time of Flight MALDI-TOF Mass Spectrometry
Published on: June 10, 2018
Related Concept Videos
Cationic Chain-Growth Polymerization: Mechanism
Radical Chain-Growth Polymerization: Chain Branching
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Anionic Chain-Growth Polymerization: Mechanism
Step-Growth Polymerization: Overview
Many natural and synthetic polymers are produced by...
Anionic Chain-Growth Polymerization: Overview