Metal‐Free Route to Precise Synthesis of Poly(propylene oxide) and Its Blocks with High Activity

The fast and living ring‐opening polymerization (ROP) of propylene oxide (PO) by metal‐free catalysis is reported. By using triethyl borane (TEB) and organic Lewis bases (LBs, e.g.: phosphazene base, amidine and guanidine) as the catalysts, various alkyl alcohols can effectively initiate the ROP of...

Full description

Saved in:
Bibliographic Details
Published inChemSusChem Vol. 11; no. 24; pp. 4209 - 4213
Main Authors Zhang, Cheng‐Jian, Duan, Han‐Yi, Hu, Lan‐Fang, Zhang, Cheng‐Hui, Zhang, Xing‐Hong
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 20.12.2018
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The fast and living ring‐opening polymerization (ROP) of propylene oxide (PO) by metal‐free catalysis is reported. By using triethyl borane (TEB) and organic Lewis bases (LBs, e.g.: phosphazene base, amidine and guanidine) as the catalysts, various alkyl alcohols can effectively initiate the ROP of PO, yielding tailor‐made poly(propylene oxide)s (PPOs) with high regioregularity, predictable molecular weights, and narrow dispersity approaching Poisson distribution. The TEB/LB catalysts present unprecedentedly high activity (turnover frequency of up to 7500 h−1) and a truly living character for the polymerization, as evidenced by kinetic studies that showed fast initiation and growth, unobserved chain‐transfer to PO, chain extension reactions, and the synthesis of various PPO‐based block copolymers with narrow dispersities (Đ<1.1). Poisson project: The metal‐free, fast, and living ring‐opening polymerization of propylene oxide is performed by a unique masking anion strategy, yielding tailor‐made poly(propylene oxide)s with unprecedented activity, high regioregularity, predictable molecular weights, and narrow dispersity approaching Poisson distribution.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1864-5631
1864-564X
1864-564X
DOI:10.1002/cssc.201802258