Abstract
A new hydrocarbon-soluble (additive-free) dicarbanionic organolithium initiator, obtained by a simple halogen-lithium exchange reaction (Gilman's reaction) from a diarylhalide containing a side C15 alkyl chain, has been designed and used to initiate the anionic polymerization of butadiene and styrene. The dilithiated species formed afford well-defined poly(styrene-b-butadiene-b-styrene) (SBS) triblock copolymers with a high percentage of 1,4-microstructure polybutadiene (91%) and excellent mechanical properties, such as ultimate tensile strength higher than 30 MPa and elongation at a break of 1000%. This represents a breakthrough in the synthesis of SBS polymers, one of the most used thermoplastic elastomers.
Original language | English (US) |
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Pages (from-to) | 8158-8159 |
Number of pages | 2 |
Journal | Journal of the American Chemical Society |
Volume | 128 |
Issue number | 25 |
DOIs | |
State | Published - Jun 28 2006 |
Externally published | Yes |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry