Aziridines and azetidines: Building blocks for polyamines by anionic and cationic ring-opening polymerization

105Citations
Citations of this article
102Readers
Mendeley users who have this article in their library.

Abstract

Despite the difficulties associated with controlling the polymerization of ring-strained nitrogen containing monomers, the resulting polymers have many important applications, such as antibacterial and antimicrobial coatings, CO2 adsorption, chelation and materials templating, and non-viral gene transfection. This review highlights the recent advances on the polymerizations of aziridine and azetidine. It provides an overview of the different routes to produce polyamines, from aziridine and azetidine, with various structures (i.e. branched vs. linear) and degrees of control. We summarize monomer preparation for cationic, anionic and other polymerization mechanisms. This comprehensive review on the polymerization of aziridine and azetidine monomers will provide a basis for the development of future macromolecular architectures using these relatively exotic monomers.

Cite

CITATION STYLE

APA

Gleede, T., Reisman, L., Rieger, E., Mbarushimana, P. C., Rupar, P. A., & Wurm, F. R. (2019, June 28). Aziridines and azetidines: Building blocks for polyamines by anionic and cationic ring-opening polymerization. Polymer Chemistry. Royal Society of Chemistry. https://doi.org/10.1039/c9py00278b

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free