Star-shaped and triblock polymers with enhanced crosslinkability

US11319396B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11319396-B2
Application numberUS-201716336660-A
CountryUS
Kind codeB2
Filing dateSep 20, 2017
Priority dateSep 27, 2016
Publication dateMay 3, 2022
Grant dateMay 3, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides compositions comprising a) at least one polymer consisting of one polymerblock A and at least two polymerblocks B, wherein each polymerblock B is attached to the polymerblock A, and wherein at least 60 mol % of the monomer units of polymerblock B are selected from the group consisting of Formulae (1A), (1B), (1C), (1D), (1E), (1F) and 1G, 1H and 1I wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are independently and at each occurrence H or C 1-10 -alkyl, and b) at least one crosslinking agent carrying at least two azide groups, as well as to layers formed from these compositions, electronic devices comprising these layers and to specific polymers encompassed by the polymers of the composition.

First claim

Opening claim text (preview).

The invention claimed is: 1. A composition, comprising: a) at least one polymer consisting of one polymer block A and at least two polymer blocks B; and b) at least one crosslinking agent carrying at least two azide groups wherein: each polymer block B is attached to the polymer block A, and at least 60 mol % of the monomer units of polymer block B are selected from the group consisting of: and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are independently and at each occurrence H or C 1-4 -alkyl, wherein the weight ratio of polymer block A/total polymer blocks B is from 70/30 to 96/4 and the polymers have a number average molecular weight Mn of at least 60000 g/mol and a weight average molecular weight Mw of at least 70000 g/mol, both as determined by gel permeation chromatography, with the proviso that at least one of the monomer units (1A) and (1B) is present, and that the ratio of [mols of monomer units (1A) and (1B)]/[mols of monomer units (1A), (1B), (1C) and (1D)] is at least 30%. 2. The composition of claim 1 , wherein: at least 70 mol % of the monomer units of the polymer block B are selected from the group consisting of:  and R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently and at each occurrence H or C 1-4 -alkyl. 3. The composition of claim 1 , wherein: at least 80 mol % of the monomer units of the polymer block B are selected from the group consisting of:  and R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are H. 4. The composition of claim 1 , wherein: at least 80 mol % of the monomer units of polymer block A are selected from the group consisting of: R 20 , R 21 , R 22 , R 23 , R 24 , R 25 and R 26 are independently and at each occurrence selected from the group consisting of H, C 6-14 -aryl, 5 to 14 membered heteroaryl and C 1-30 -alkyl; R a is C(O)OH, C(O)OC 1-30 -alkyl, C(O)—H, C(O)C 6-14 -aryl, C(O)N(C 1-30 -alkyl) 2 , C(O)N(C 6-14 -aryl) 2 , C(O)N(C 1-30 -alkyl)(C 6-14 -aryl), C(O)—C 6-14 -aryl, C(O)—C 1-30 -alkyl, O—C 6-14 -aryl, O—C 1-30 -alkyl, OC(O)C 1-30 -alkyl, OC(O)C 6-14 -aryl or CN; C 6-14 -aryl and 5-14 membered heteroaryl can be substituted with one or more substituents selected from the group consisting of C 1-10 -alkyl, C(O)OH, C(O)OC 1-10 -alkyl, C(O)phenyl, C(O)N(C 1-10 -alkyl) 2 , C(O)N(phenyl) 2 , C(O)N(C 1-10 -alkyl)(phenyl), C(O)-phenyl, C(O)—C 1-10 -alkyl, OH, O-phenyl, O—C 1-10 -alkyl, OC(O)C 1-10 -alkyl, OC(O)-phenyl and CN and NO 2 ; C 1-30 -alkyl can be substituted with one or more substituents selected from the group consisting of with phenyl, C(O)OH, C(O)OC 1-10 -alkyl, C(O)phenyl, C(O)N(C 1-10 -alkyl) 2 , C(O)N(phenyl) 2 , C(O)N(C 1-10 -alkyl)(phenyl), C(O)-phenyl, C(O)—C 1-10 -alkyl, O-phenyl, O—C 1-10 -alkyl, OC(O)C 1-10 -alkyl, OC(O)-phenyl, Si(C 1-10 -alkyl) 3 , Si(phenyl) 3 and CN and NO 2 ; n is an integer from 1 to 3; and L 20 is C 1-10 -alkylene, C 2-10 -alkenylene, C 2-10 -alkynylene, C 6-14 -arylene or S(O). 5. The composition according to claim 1 , wherein: at least 80 mol % of the monomer units of polymer block A are selected from the group consisting of: R 20 , R 21 and R 22 are independently selected from the group consisting of H, C 6-14 -aryl, 5 to 14 membered heteroaryl and C 1-30 -alkyl; R a is C(O)OC 1-30 -alkyl; C 6-14 -aryl and 5-14 membered heteroaryl can be substituted with one or more C 1-10 -alkyl; C 1-30 -alkyl can be substituted with one or more substituents selected from the group consisting of Si(C 1-10 -alkyl) 3 and Si(phenyl) 3 ; n is an integer from 1 to 3; and L 20 is C 1-10 -alkylene or C 6-14 -arylene. 6. The composition of claim 1 , wherein: at least 90 mol % of the monomer units of polymer block A is a monomer unit selected from the group consisting of: R 20 and R 21 are independently selected from the group consisting of H and C 6-14 -aryl; C 6-14 -aryl can be substituted with one or more C 1-10 -alkyl; and L 20 is C 6-14 -arylene. 7. The composition of claim 1 , wherein: the crosslinking agent carrying at least two azide groups is of formula: a is 0 or 1; R 50 is at each occurrence selected from the group consisting of H, halogen, SO 3 M and C 1-20 -alkyl, which C 1-20 -alkyl can be substituted with one or more halogen, wherein M is H, Na, K or Li; and L 50 is a linking group. 8. The composition of claim 7 , wherein: L 50 is a linking group of formula: b, c, d, e, f, g and h are independently from each other 0 or 1, provided that b, c, d, e, f, g and h are not all at the same time 0; W 1 , W 2 , W 3 and W 4 are independently selected from the group consisting of C(O), C(O)O, C(O)—NR 51 , SO 2 —NR 51 , NR 51 , N + R 51 R 51 , CR 51 ═CR 51 and ethynylene; R 51 is at each occurrence H or C 1-10 -alkyl, or two R 51 groups, which can be from different W 1 , W 2 , W 3 and W 4 groups, together with the connecting atoms form a 5, 6 or 7 membered ring, which may be substituted with one to three C 1-6 -alkyl; Z 1 , Z 2 and Z 3 are independently selected from the group consisting of C 1-10 -alkylene, C 5-8 -cycloalkylene, C 6-14 -arylene, 5 to 14 membered heteroarylene, and polycyclic system containing at least one ring selected from C 6-14 -aromatic ring and 5 to 14 membered heteroaromatic ring; and C 1-10 -alkylene, C 5-8 -cycloalkylene, C 6-14 membered arylene, 5 to 14 membered heteroarylene and polycyclic system containing at least one ring selected from C 6-14 -aromatic ring and 5 to 14 membered heteroaromatic ring substituted with one to five C 1-20 -alkyl or phenyl. 9. The composition of claim 1 , further comprising a solvent. 10. The composition of claim 8 , wherein the composition is a solution and comprises; i) 0.1 to 500 mg of the at least one polymer based on 1000 mg of the composition; ii) 0.1 to 20% by weight of the at least one crosslinking agent carrying at least two azide groups based on the weight of the one or more polymers; and iii) a solvent. 11. A cured layer formed from the composition of claim 1 . 12. An electronic device, comprising the cured layer of claim 11 . 13. The electronic device of claim 12 , wherein: the electronic device is an organic field effect transistor; and the layer is the dielectric layer.

Assignees

Inventors

Classifications

  • C08F297/04Primary

    polymerising vinyl aromatic monomers and conjugated dienes · CPC title

  • C08K5/0025Primary

    Crosslinking or vulcanising agents; including accelerators · CPC title

  • leading to a crosslinking, either explicitly or inherently · CPC title

  • Electricity · mapped topic

  • C08K5/28Primary

    Azides · CPC title

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What does patent US11319396B2 cover?
The present invention provides compositions comprising a) at least one polymer consisting of one polymerblock A and at least two polymerblocks B, wherein each polymerblock B is attached to the polymerblock A, and wherein at least 60 mol % of the monomer units of polymerblock B are selected from the group consisting of Formulae (1A), (1B), (1C), (1D), (1E), (1F) and 1G, 1H and 1I wherein R 1 , R…
Who is the assignee on this patent?
Basf Se
What technology area does this patent fall under?
Primary CPC classification C08F297/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).