IP Library › Granted Patent US 12,727,375
Granted Patent B2
US 12,727,375 · App. 17/899,771 · Granted Sep 1, 2026

Polymer, a composition, and an electroluminescent device

Inventors: Masashi Tsuji (Hwaseong-si, KR); Norihito Ishii (Kanagawa-ken, JP); Takahiro Fujiyama (Yokohama, JP); Naotoshi Suganuma (Kanagawa-ken, JP); Yusaku Konishi (Yokohama, JP); Fumiaki Kato (Yokohama, JP)
Assignee: SAMSUNG ELECTRONICS CO., LTD.
H10K85/111C08G61/12H10K50/11H10K85/115H10K85/151C08G2261/143C08G2261/148C08G2261/3142C08G2261/3162H10K50/115H10K2101/40
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Quick Facts
Patent No.
US 12,727,375
App. No.
17/899,771
Granted
Sep 1, 2026
Kind
B2
Abstract

As a means for providing an electroluminescent device capable of achieving high luminance, high efficiency, and at the same time excellent device life-span, a polymer having an overlap index of greater than or equal to about 0.00001 and less than or equal to about 1.8, and a polymer including a structural unit represented by Chemical Formula (1) are provided:

Claims (80)

1 . A polymer comprising a structural unit represented by Chemical Formula (1):

wherein, in Chemical Formula (1),

Ar 1 and Ar 2 are each independently a substituted or unsubstituted divalent aromatic hydrocarbon group having 6 to 60 carbon atoms,

Ar 3 is selected from Group (I):

wherein, in Group (I),

R 111 to R 123 are each independently a hydrogen atom or a linear or branched hydrocarbon group having 1 to 16 carbon atoms, and

* indicates a bonding position with an adjacent atom,

Ar 4 is a substituted or unsubstituted divalent aromatic hydrocarbon group having 6 to 60 carbon atoms or a substituted or unsubstituted divalent aromatic heterocyclic ring group having 3 to 60 ring atoms,

Ar 5 is a single bond or a substituted or unsubstituted divalent aromatic heterocyclic ring group having 3 to 60 ring atoms,

each R 1 is independently a hydrogen atom, an alkyl group, a hydroxyalkyl group, an alkylthiol group, an alkoxy group, an alkoxyalkyl group, an alkylthioalkyl group, an alkenyl group, an alkynyl group, an alkylthio group, an alkoxycarbonyl group, an alkylthiocarbonyl group, a hydroxyl group, a carboxyl group, a thiocarboxyl group, a dithiocarboxyl group, a thiol group, or a cyano group,

each R 2 is independently a hydrogen atom, an alkyl group, a hydroxyalkyl group, an alkylthiol group, an alkoxy group, an alkoxyalkyl group, an alkylthioalkyl group, an alkenyl group, an alkynyl group, an alkylthio group, an alkoxycarbonyl group, an alkylthiocarbonyl group, a hydroxyl group, a carboxyl group, a thiocarboxyl group, a dithiocarboxyl group, a thiol group, a cyano group, and

A is a structure represented by Chemical Formula (2) or Chemical Formula (3):

wherein, in Chemical Formula (2),

each Ar 6 is independently a hydrogen atom, an alkyl group, a hydroxyalkyl group, an alkoxy group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an alkylthio group, an alkoxycarbonyl group, an alkylthiol group, an alkylthiocarbonyl group, a thiocarboxyl group, a dithiocarboxyl group, an alkylthioalkyl group, a hydroxyl group, a carboxyl group, a thiol group, a cyano group, a substituted or unsubstituted monovalent aromatic hydrocarbon group having 6 to 60 carbon atoms, a substituted or unsubstituted monovalent aromatic heterocyclic ring group having 3 to 60 ring atoms, or a substituted or unsubstituted monovalent ring set group including a structure in which one or more aromatic hydrocarbon rings having 6 to 60 carbon atoms and one or more aromatic heterocyclic rings having 3 to 60 ring atoms are bonded through a single bond,

each Ar 7 is independently a hydrogen atom, an alkyl group, a hydroxyalkyl group, an alkoxy group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an alkylthio group, an alkoxycarbonyl group, an alkylthiol group, an alkylthiocarbonyl group, a thiocarboxyl group, a dithiocarboxyl group, an alkylthioalkyl group, a hydroxyl group, a carboxyl group, a thiol group, a cyano group, a substituted or unsubstituted monovalent aromatic hydrocarbon group having 6 to 60 carbon atoms, a substituted or unsubstituted monovalent aromatic heterocyclic ring group having 3 to 60 ring atoms, or a substituted or unsubstituted monovalent ring set group including a structure in which one or more aromatic hydrocarbon rings having 6 to 60 carbon atoms and one or more aromatic heterocyclic rings having 3 to 60 ring atoms are bonded through a single bond,

two or more Ar 7 s optionally form a condensed ring with the benzene ring to which two or more Ar 7 are bonded, and

* indicates a bonding position with an adjacent atom;

wherein, in Chemical Formula (3),

each Ar 8 is independently a hydrogen atom, an alkyl group, a hydroxyalkyl group, an alkoxy group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an alkylthio group, an alkoxycarbonyl group, an alkylthiol group, an alkylthiocarbonyl group, a thiocarboxyl group, a dithiocarboxyl group, an alkylthioalkyl group, a hydroxyl group, a carboxyl group, a thiol group, a cyano group, a substituted or unsubstituted monovalent aromatic hydrocarbon group having 6 to 60 carbon atoms, a substituted or unsubstituted monovalent aromatic heterocyclic ring group having 3 to 60 ring atoms, or a substituted or unsubstituted monovalent ring set group including a structure in which one or more aromatic hydrocarbon rings having 6 to 60 carbon atoms and one or more aromatic heterocyclic rings having 3 to 60 ring atoms are bonded through a single bond,

each Ar 9 is independently a hydrogen atom, an alkyl group, a hydroxyalkyl group, an alkoxy group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an alkylthio group, an alkoxycarbonyl group, an alkylthiol group, an alkylthiocarbonyl group, a thiocarboxyl group, a dithiocarboxyl group, an alkylthioalkyl group, a hydroxyl group, a carboxyl group, a thiol group, a cyano group, a substituted or unsubstituted monovalent aromatic hydrocarbon group having 6 to 60 carbon atoms, a substituted or unsubstituted monovalent aromatic heterocyclic ring group having 3 to 60 ring atoms, or a substituted or unsubstituted monovalent ring set group including a structure in which one or more aromatic hydrocarbon rings having 6 to 60 carbon atoms and one or more aromatic heterocyclic rings having 3 to 60 ring atoms are bonded through a single bond,

X is S, O, or C substituted with two substituted or unsubstituted linear or branched hydrocarbon groups having 1 to 16 carbon atoms,

two or more Ar 9 s optionally form a condensed ring with the benzene ring to which two or more Ar 9 s are bonded, and

* indicates a bonding position with an adjacent atom.

2 . The polymer of claim 1 , wherein at least one of Ar 1 , Ar 2 , and Ar 4 in Chemical Formula (1) is each independently a group selected from Group (II):

wherein R 211 to R 225 are each independently a hydrogen atom, or linear or branched hydrocarbon group having 1 to 16 carbon atoms, and

* indicates a bonding position with an adjacent atom.

3 . The polymer of claim 2 , wherein in Chemical Formula (1), Ar 1 , Ar 2 , and Ar 4 are each independently a group selected from Group (II).

4 . A polymer comprising at least one structural unit selected from Group (A);

wherein, in the chemical formulas of Group (A), n represents an integer,

when the compounds represented by the chemical formulas have two or more groups represented by “C n H 2n+1 —”,

n in each “C n H 2n+1 —” is the same as or different from each other, and

each group represented by “C n H 2n+1 —” is the same as or different from each other.

5 . The polymer of claim 4 , wherein the structural unit is at least one structural unit selected from Group (B):

wherein, in the above chemical formulas, the group represented by “C 12 H 25 -” represents an n-dodecyl group,

the group represented by “C 10 H 21 —” represents an n-decyl group,

the group represented by “C 8 H 17 —” represents an n-octyl group, and

the group represented by “C 6 H 13 —” represents an n-hexyl group.

6 . The polymer of claim 4 , wherein the structural unit is at least one structural unit selected from Group (B′):

wherein, in the above chemical formulas, the group represented by “C 8 H 17 —” represents an n-octyl group.

7 . A composition comprising the polymer of claim 1 .

8 . The composition of claim 7 , wherein the composition further comprises a low molecular weight material satisfying the following condition (a) and at the same time satisfying the following condition (b), the following condition (c), or a combination thereof:

(a) a band gap of the low molecular weight material is larger than the polymer,

(b) a LUMO of the low molecular weight material is shallower than the LUMO of the polymer, and

(c) a HOMO of the low molecular weight material is deeper than the HOMO of the polymer.

9 . An electroluminescent device comprising

a pair of electrodes, and at least one organic film comprising the polymer of claim 1 .

10 . An electroluminescent device comprising a pair of electrodes, and one or two or more organic layers comprising, wherein at least one the organic layer comprises the polymer of claim 1 , and a low molecular weight material satisfying the following condition (a) and satisfying the following condition (b), the following condition (c), or a combination thereof:

(a) a band gap of the low molecular weight material is larger than the polymer,

(b) a LUMO of the low molecular weight material is shallower than the polymer, and

(c) a HOMO of the low molecular weight material is deeper than the polymer.

11 . An electroluminescent device comprising

a pair of electrodes, and at least one organic film comprising the composition of claim 7 .

12 . The electroluminescent device of claim 9 , wherein the electroluminescent device further comprises a layer comprising quantum dots.

13 . The electroluminescent device of claim 10 , wherein the electroluminescent device further comprises a layer comprising quantum dots.

14 . The electroluminescent device of claim 11 , wherein the electroluminescent device further comprises a layer comprising quantum dots.

15 . The polymer of claim 1 , wherein the polymer has an overlap index of greater than or equal to about 0.00001 and less than or equal to about 1.8 represented by the following equation:

overlap

⁢

index

=

(

∑

k

=

1

n

(

d

HOMO

k

×

d

LUMO

k

)

)

×

100

wherein, in the equation, k is a serial number assigned to an atom in the chemical formula of a structural unit constituting the polymer, d k HOMO denotes a distribution density of the HOMO in the atom of serial number k, and d k LUMO denotes a distribution density of the LUMO in the atom of serial number k.

16 . The polymer of claim 15 , wherein the overlap index of greater than or equal to about 0.00001 and less than or equal to about 1.2.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2022
From: TSUJI, MASASHI; ISHII, NORIHITO; FUJIYAMA, TAKAHIRO; SUGANUMA, NAOTOSHI; KONISHI, YUSAKU; KATO, FUMIAKI
To: SAMSUNG ELECTRONICS CO., LTD.
Reel/Frame 060975/0634 →
Priority Claims (3)
JP 2021-141633 · Aug 31, 2021 · national
JP 2022-122163 · Jul 29, 2022 · national
KR 10-2022-0108733 · Aug 29, 2022 · national
Continuity (1)
Related Publication 20230126748A1 · Apr 27, 2023
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