Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene

A novel alkyl lithium-based initiator with relatively large steric hindrance, tert-butyldimethylsiloxydimethylpropyl lithium (TBDMSODPrLi), was designed and synthesized. By using TBDMSODPrLi, hydroxyl-terminated polybutadiene (HTPB) was prepared via anionic polymerization. The macromolecular structu...

Full description

Bibliographic Details
Main Authors: Xin Min, Xiaodong Fan, Jie Liu
Format: Article
Language:English
Published: The Royal Society 2018-01-01
Series:Royal Society Open Science
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.180156
Description
Summary:A novel alkyl lithium-based initiator with relatively large steric hindrance, tert-butyldimethylsiloxydimethylpropyl lithium (TBDMSODPrLi), was designed and synthesized. By using TBDMSODPrLi, hydroxyl-terminated polybutadiene (HTPB) was prepared via anionic polymerization. The macromolecular structure of HTPB was characterized and verified by FTIR and 1H-NMR. It was found that 1,4 unit content in HTPB initiated by TBDMSODPrLi was significantly higher (over 90%) compared to a HTPB (1,4 unit content of 70%) initiated with another initiator possessing smaller steric hindrance. The possible mechanism, which was based on initiator steric hindrance affecting monomer chain addition behaviour, was deduced. It was that the initiator's larger steric hindrance blocked lithium's intermolecular association during anionic polymerization; as a result, it could effectively increase the 1,4 unit content in HTPB. To further study how to obtain higher and stable 1,4 unit content, the optimal anionic polymerization technique for HTPB was explored including polymerization temperature, time and the amount of initiator used. The study concluded that utilization of an initiator with larger steric hindrance and reducing the polymerization temperature were two important factors to raise the 1,4 unit content in HTPB.
ISSN:2054-5703