Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Min, Xin, Fan, Xiaodong, Liu, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990791/
https://www.ncbi.nlm.nih.gov/pubmed/29892450
http://dx.doi.org/10.1098/rsos.180156
_version_ 1783329649587126272
author Min, Xin
Fan, Xiaodong
Liu, Jie
author_facet Min, Xin
Fan, Xiaodong
Liu, Jie
author_sort Min, Xin
collection PubMed
description 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 (1)H-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.
format Online
Article
Text
id pubmed-5990791
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher The Royal Society Publishing
record_format MEDLINE/PubMed
spelling pubmed-59907912018-06-11 Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene Min, Xin Fan, Xiaodong Liu, Jie R Soc Open Sci Chemistry 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 (1)H-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. The Royal Society Publishing 2018-05-30 /pmc/articles/PMC5990791/ /pubmed/29892450 http://dx.doi.org/10.1098/rsos.180156 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Min, Xin
Fan, Xiaodong
Liu, Jie
Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
title Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
title_full Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
title_fullStr Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
title_full_unstemmed Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
title_short Utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
title_sort utilization of steric hindrance of alkyl lithium-based initiator to synthesize high 1,4 unit-containing hydroxyl- terminated polybutadiene
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990791/
https://www.ncbi.nlm.nih.gov/pubmed/29892450
http://dx.doi.org/10.1098/rsos.180156
work_keys_str_mv AT minxin utilizationofsterichindranceofalkyllithiumbasedinitiatortosynthesizehigh14unitcontaininghydroxylterminatedpolybutadiene
AT fanxiaodong utilizationofsterichindranceofalkyllithiumbasedinitiatortosynthesizehigh14unitcontaininghydroxylterminatedpolybutadiene
AT liujie utilizationofsterichindranceofalkyllithiumbasedinitiatortosynthesizehigh14unitcontaininghydroxylterminatedpolybutadiene