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US-12140831-B2 · Nov 12, 2024 · US
US10247867B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10247867-B2 |
| Application number | US-201615242862-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 22, 2016 |
| Priority date | Aug 28, 2015 |
| Publication date | Apr 2, 2019 |
| Grant date | Apr 2, 2019 |
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A monomer represented by Chemical Formula 1-1 wherein in Chemical Formula 1-1, Z, L 1 , L 2 , R 1 to R 6 , n, m, p, and a to f are the same as defined in the detailed description.
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What is claimed is: 1. A polymer, which is a reaction product of an anhydride and a diamine compound, wherein the diamine compound comprises a first diamine compound represented by Chemical Formula 1-1: wherein, in Chemical Formula 1-1, Z is —C═O—, —(C═O)O—, —O(C═O)—, —CH 2 O—, —CF 2 O—, —OC(═O)O—, —C≡C—, —CH═CH—, —CF═CF—, or —C(═O)NR a —, L 1 and L 2 are independently a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C1 to C20 oxyalkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C3 to C20 oxycycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C6 to C20 oxyarylene group, a substituted or unsubstituted C3 to C20 divalent heterocyclic group, or a combination thereof, R 1 to R 6 and R a are independently hydrogen, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C1 to C20 alkoxy group, a substituted or unsubstituted C2 to C20 alkoxyalkyl group, a substituted or unsubstituted C1 to C20 fluoroalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyloxy group, a substituted or unsubstituted C4 to C20 cycloalkoxyalkyl group, a substituted or unsubstituted C6 to C20 aryl group, a substituted or unsubstituted C6 to C20 aryloxy group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C7 to C20 aryloxyalkyl group, a substituted or unsubstituted C3 to C20 heterocyclic group, a substituted or unsubstituted silyl group, a hydroxy group, a halogen, a nitro group, or a combination thereof, n and m are independently 0 or 1, p is an integer ranging from 1 to 3, a to f are independently integers ranging from 0 to 4, and a+b, c+d, and e+f are independently integers of less than or equal to 4. 2. The polymer of claim 1 , wherein the first diamine compound is represented by Chemical Formula 1-1a or 1-1b: wherein, in Chemical Formulae 1-1a and 1-1b, Z is —C═O—, —(C═O)O—, —O(C═O)—, —CH 2 O—, —CF 2 O—, —OC(═O)O—, —C≡C—, —CH═CH—, —CF═CF—, or —C(═O)NR a —, L 1 and L 2 are independently a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C1 to C20 oxyalkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C3 to C20 oxycycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C6 to C20 oxyarylene group, a substituted or unsubstituted C3 to C20 divalent heterocyclic group, or a combination thereof, R 1 to R 6 and R a are independently hydrogen, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C1 to C20 alkoxy group, a substituted or unsubstituted C2 to C20 alkoxyalkyl group, a substituted or unsubstituted C1 to C20 fluoroalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyloxy group, a substituted or unsubstituted C4 to C20 cycloalkoxyalkyl group, a substituted or unsubstituted C6 to C20 aryl group, a substituted or unsubstituted C6 to C20 aryloxy group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C7 to C20 aryloxyalkyl group, a substituted or unsubstituted C3 to C20 heterocyclic group, a substituted or unsubstituted silyl group, a hydroxy group, a halogen, a nitro group, or a combination thereof, p is an integer ranging from 1 to 3, a to f are independently integers ranging from 0 to 4, and a+b, c+d, and e+f are independently integers of less than or equal to 4. 3. The polymer of claim 1 , wherein the first diamine compound is represented by Chemical Formula 1a or 1b: 4. The polymer of claim 1 , wherein the diamine compound further comprises a second diamine compound, which is different from the first diamine compound, and wherein the second diamine compound comprises at least one selected from compounds of Group 1: wherein, in Group 1, R 32 to R 48 are independently hydrogen, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C1 to C20 alkoxy group, a substituted or unsubstituted C1 to C20 fluoroalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyl group, a substituted or unsubstituted C3 to C20 heterocyclic group, a substituted or unsubstituted C3 to C20 cycloalkoxy group, a substituted or unsubstituted C6 to C20 aryl group, a substituted or unsubstituted C6 to C20 aryloxy group, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C20 alkylamine group, a substituted or unsubstituted silyl group, a hydroxy group, a halogen, a nitro group, or a combination thereof, X 2 to X 10 are independently a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C3 to C20 divalent heterocyclic group, —SO 2 —, —O—, —C(═O)—, —C(═O)O—, a group selected from Group 2, or a combination thereof, n35 to n37 and n40 to n49 are independently an integer ranging from 0 to 4, and n38 and n39 are independently an integer ranging from 0 to 3, 5. The polymer of claim 4 , wherein the second diamine compound comprises at least one selected from compounds of Group 3: 6. The polymer of claim 4 , wherein a mole ratio of the first diamine compound and the second diamine compound is about 1:9 to about 5:5. 7. The polymer of claim 1 , wherein the anhydride is represented by Chemical Formula 2 or 3: wherein, in Chemical Formula 2 or 3, L 3 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C1 to C20 oxyalkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C3 to C20 oxycycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C6 to C20 oxyarylene group, a substituted or unsubstituted C3 to C20 divalent heterocyclic group, —O—, —C(═O)—, —C(═O)O—, —SO 2 —, —C(═O)NR b —, or a combination thereof, and R 7 to R 12 and R b are independently hydrogen, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C1 to C20 alkoxy group, a substituted or unsubstituted C2 to C20 alkoxyalkyl group, a substituted or unsubstituted C1 to C20 fluoroalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyl group, a substituted or unsubstituted C3 to C20 cycloalkyloxy group, a substituted or unsubstituted C4 to C20 cycloalkoxyalkyl group, a substituted
Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors · CPC title
with oxygen only in the tetracarboxylic moiety · CPC title
with amino and carboxyl groups bound in meta- or para- positions · CPC title
wholly aromatic in the tetracarboxylic moiety · CPC title
from tetracarboxylic acids or derivatives and diamines · CPC title
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