Stereoregular diblock polybutadienes having a 1,4-cis/syndiotactic 1,2 structure from stereospecific polymerization
US-10066044-B2 · Sep 4, 2018 · US
US11261281B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11261281-B2 |
| Application number | US-201816652348-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 11, 2018 |
| Priority date | Oct 19, 2017 |
| Publication date | Mar 1, 2022 |
| Grant date | Mar 1, 2022 |
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A block polymer comprising a first block and a second block is provided. The first block contains aromatic α-mono-olefin units, and the second block contains both 1,3-diene units and mono-olefin units.
Opening claim text (preview).
The invention claimed is: 1. A block polymer comprising: a first block and a second block, the first block comprising monomer units of a first aromatic α-mono-olefin, the first aromatic α-mono-olefin being of formula CH 2 ═CH—Ar, Ar representing a substituted or unsubstituted aromatic group, the second block comprising monomer units of a second 1,3-diene and monomer units of a second olefin selected from the group consisting of ethylene, α-mono-olefins and their mixtures, provided that, if the second block is a copolymer chain of a 1,3-diene and of an aromatic α-mono-olefin of formula CH 2 ═CH—Ar′, Ar′ representing a substituted or unsubstituted aromatic group, the diene units of trans-1,4-structure in the second block represent more than 80 mol % of the diene units of 1,4-structure of the second block, and the block polymer containing 1,2-cyclohexanediyl units. 2. The block polymer according to claim 1 , in which the Ar group and the Ar′ group are, independently of one another, a phenyl group or an aryl group. 3. The block polymer according to claim 1 , which block polymer is a diblock. 4. The block polymer polymer according to claim 1 , in which the first aromatic α-mono-olefin is styrene. 5. The block polymer polymer according to claim 1 , in which the first block comprises more than 0 mol % to 100 mol % of units of the first aromatic α-mono-olefin and from 0 mol % to less than 100 mol % of units of a first 1,3-diene. 6. The block polymer according to claim 5 , in which the first 1,3-diene is 1,3-butadiene, isoprene or their mixture. 7. The block polymer according to claim 1 , in which the first block is a homopolymer chain of the first aromatic α-mono-olefin. 8. The block polymer according to claim 5 , in which the first block is a copolymer chain of the first aromatic α-mono-olefin and of the first 1,3-diene. 9. The block polymer according to claim 1 , in which the first block contains more than 10 monomer units. 10. The block polymer according to claim 1 , in which the first block is an atactic chain. 11. The block polymer according to claim 1 , in which the second block comprises more than 0 mol % to 50 mol % of the monomer units of the second 1,3-diene and from 50 mol % to less than 100 mol % of the monomer units of the second olefin. 12. The block polymer according to claim 1 , in which the diene units of trans-1,4-structure in the second block represent more than 80 mol % of the diene units of 1,4-structure of the second block. 13. The block polymer according to claim 1 , in which the diene units of trans-1,4-structure in the block polymer represent more than 70 mol % of the diene units of 1,4-structure of the block polymer. 14. The block polymer according to claim 1 , in which the second 1,3-diene is 1,3-butadiene. 15. The block polymer according to claim 1 , in which the second block is a copolymer chain of 1,3-butadiene and of ethylene or a terpolymer chain of 1,3-butadiene, of ethylene and of an α-mono-olefin. 16. The block polymer according to claim 1 , in which the first block is covalently bonded to the second block by direct joining of a carbon atom of a monomer unit of the first block to a carbon atom of a monomer unit of the second block. 17. The block polymer according to claim 1 , in which the first block includes an atactic polystyrene, and the second block includes a copolymer of 1,3-butadiene and of ethylene (EB).
using a catalyst of the coordination type · CPC title
selected from boron, aluminium, gallium, indium, thallium or rare earths (C08F4/14 takes precedence) · CPC title
Macromolecular compounds obtained by polymerisation using successively different catalyst types without deactivating the intermediate polymer · CPC title
Butadiene · CPC title
using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title
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