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A novel synthetic strategy for styrene–butadiene–styrene tri-block copolymer with high cis-1,4 units via changing catalytic active centres
- Source :
- Royal Society Open Science, Vol 6, Iss 6 (2019), Royal Society Open Science
- Publication Year :
- 2019
- Publisher :
- The Royal Society, 2019.
-
Abstract
- A styrene–butadiene–styrene tri-block copolymer (SBS) with a high cis -1,4 unit content (greater than 97%) was synthesized by a novel synthetic strategy based on changing the catalytic active centres using n -butyllithium and a nickel-based catalyst. Firstly, styrene was polymerized via anionic polymerization using butyllithium as the initiator (Li, activity centre Li) at 50°C. The obtained alkylated macroinitiator (PSLi) was aged with nickel naphthenate (Ni) and boron trifluoride etherate (B) to prepare a second reactive centre (Ni-F), which was used to initiate the polymerization of butadiene (Bd). Finally, triphenyl phosphine (PPh 3 ) was added to adjust the electron density of the third active centre (P-Ni-F), and styrene monomer was added again to synthesize the second polystyrene block to obtain SBS. The polymerization technique presented here is simple and has an efficient initiation effect due to the high initiation activities for the different monomers. It also exhibits excellent control over the stereo-structure of the butadiene segments in the prepared copolymers, and the SBS polymers with high cis -1,4 unit content were easily achieved.
- Subjects :
- Materials science
Styrene-butadiene
02 engineering and technology
01 natural sciences
Styrene
high cis-1,4 unit
chemistry.chemical_compound
butadiene
Polymer chemistry
Copolymer
Butyllithium
lcsh:Science
tri-block copolymer
Multidisciplinary
010405 organic chemistry
catalytic active centre
021001 nanoscience & nanotechnology
0104 chemical sciences
Chemistry
Monomer
Anionic addition polymerization
chemistry
Polymerization
styrene
lcsh:Q
Polystyrene
0210 nano-technology
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 20545703
- Volume :
- 6
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Royal Society Open Science
- Accession number :
- edsair.doi.dedup.....cfc6ebac3672f103017d724d7b984dd7
- Full Text :
- https://doi.org/10.1098/rsos.190536