Accelerated Polypeptide Synthesis via N‐Carboxyanhydride Ring Opening Polymerization in Continuous Flow

In nature, polypeptide‐based materials are ubiquitous, yet their synthetic production is hampered by high cost, limited scalability, and often stringent reaction conditions. Herein an elegant approach is presented for N‐carboxyanhydride ring opening polymerization (NCA ROP) of Nε‐benzyloxycarbonyl‐l...

Full description

Saved in:
Bibliographic Details
Published in:Macromolecular rapid communications. Vol. 41; no. 18; pp. e2000071 - n/a
Main Authors: Vrijsen, Jeroen Hendrik, Rasines Mazo, Alicia, Junkers, Tanja, Qiao, Greg Guanghua
Format: Journal Article
Language:English
Published: Weinheim Wiley Subscription Services, Inc 01-09-2020
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:In nature, polypeptide‐based materials are ubiquitous, yet their synthetic production is hampered by high cost, limited scalability, and often stringent reaction conditions. Herein an elegant approach is presented for N‐carboxyanhydride ring opening polymerization (NCA ROP) of Nε‐benzyloxycarbonyl‐l‐lysine (ZLL) and γ‐benzyl‐l‐glutamate (BLG) NCA in continuous flow. The polymerization is initiated by primary amine initiators using N,N‐dimethylformamide (DMF) as solvent. Carrying out the reaction in a silicon microflow reactor speeds up the rate of ROP (92% conversion in 40 min in flow as opposed to 6 h in batch) due to highly efficient permeation of CO2 through the reactor tubing. The polymerization strategy provides a facile, scale‐up friendly alternative to traditional batch mode polymerization and has the capability of streamlining NCA ROP. N‐carboxyanhydride ring opening polymerization in traditional systems often suffers from slow polymerization. Substantial acceleration is observed in this work by performing the polymerization in a silicon microflow reactor due to more efficient removal of the CO2 byproduct. This continuous flow proof of concept can further stimulate the use of continuous flow for polypeptide synthesis potentially streamlining N‐carboxyanhydride ring opening polymerization.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1022-1336
1521-3927
DOI:10.1002/marc.202000071