IP Library › Granted Patent US 10,800,970
Granted Patent B2
US 10,800,970 · App. 15/745,323 · Granted Oct 13, 2020

Color conversion composition, color conversion film and backlight unit, display and lighting device each comprising same

Inventors: Hirotoshi Sakaino (Shiga, JP); Daisaku Tanaka (Shiga, JP)
Assignee: TORAY INDUSTRIES, INC.
C09K11/06C09K11/02F21V9/30H01L33/501H01L33/502C09K2211/1018C09K2211/1022F21Y2115/10
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Quick Facts
Patent No.
US 10,800,970
App. No.
15/745,323
Granted
Oct 13, 2020
Kind
B2
Abstract

A color conversion composition converting incident light to light having a longer wavelength than the incident light, and containing the following components (A)-(C): (A) at least one luminescent material; (B) a binder resin; and (C) at least one of tertiary amines, catechol derivatives and nickel compounds, in which the tertiary amines, the catechol derivatives and the nickel compounds have a molar extinction coefficient ε of 100 or less over the whole wavelength range from 400 nm to 800 nm is provided. This color conversion composition achieves a good balance between improvement of color reproducibility and durability if used for a liquid crystal display or an LED lighting device.

Claims (30)

1. A color conversion composition for converting incident light into light having longer wavelength than the incident light,

wherein the color conversion composition comprises the following components (A) to (C):

(A) at least one luminescent material,

(B) a binder resin, and

(c) at least one of a tertiary amine, a catechol derivative and a nickel compound, and

wherein the tertiary amine, catechol derivative and nickel compound have a molar extinction coefficient ε of 100 or less in the whole wavelength region from 400 nm to 800 nm.

2. The color conversion composition according to claim 1 , wherein the component (C) contains a nickel compound and the nickel compound is at least one of a nickel salt of an organic acid, an acetylacetonate-based nickel complex, and a thiobisphenolate-based nickel complex.

3. The color conversion composition according to claim 1 , wherein the component (C) contains a nickel compound and a content of the nickel compound is from 1.0×10 −2 to 10 parts by weight per 100 parts by weight of the component (B).

4. The color conversion composition according to claim 1 , wherein the component (C) contains a tertiary amine and at least one substituent on a nitrogen atom of the tertiary amine is a substituted or unsubstituted alkyl group.

5. The color conversion composition according to claim 1 , wherein the content of the component (C) is from 10 −2 to 15 parts by weight per 100 parts by weight of the component (B).

6. The color conversion composition according to claim 1 , wherein the luminescent material contains a luminescent material which emits light having a peak wavelength of 500 to 580 nm by use of excitation light having a wavelength of 430 to 500 nm.

7. The color conversion composition according to claim 1 , wherein the luminescent material contains the following luminescent materials (a) and (b):

(a) a luminescent material that emits light having a peak wavelength of 500 to 580 nm by use of excitation light having a wavelength of 430 to 500 nm, and

(b) a luminescent material that emits light having a peak wavelength of 580 to 750 nm upon being excited by either one or both of excitation light having a wavelength of 430 to 500 nm and light emitted by the luminescent material (a).

8. The color conversion composition according to claim 7 , wherein a content w a of the luminescent material (a) and a content w b of the luminescent material (b) are in the relationship of w a ≥w b .

9. The color conversion composition according to claim 1 , wherein the luminescent material contains a compound represented by formula (1):

(wherein X is C—R 7 or N, and each of R 1 to R 9 , which may be the same as or different from one another, is selected from hydrogen, an alkyl group, a cycloalkyl group, a heterocyclic group, an alkenyl group, a cycloalkenyl group, an alkynyl group, a hydroxyl group, a thiol group, an alkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, an aryl group, a heteroaryl group, a halogen, a cyano group, an aldehyde group, a carbonyl group, a carboxyl group, an oxycarbonyl group, a carbamoyl group, an amino group, a nitro group, a silyl group, a siloxanyl group, a boryl group, a phosphine oxide group, and a fused ring and an aliphatic ring each formed between adjacent substituents).

10. The color conversion composition according to claim 9 , wherein in the formula (1), X is C—R 7 and R 7 is a substituted or unsubstituted aryl group.

11. The color conversion composition according to claim 9 , wherein in the formula (1), X is C—R 7 and R 7 is a substituted or unsubstituted phenyl group.

12. The color conversion composition according to claim 7 , wherein the luminescent material (a) is a compound represented by the formula (1):

(wherein X is C—R 7 or N, and each of R 1 to R 9 , which may be the same as or different from one another, is selected from hydrogen, an alkyl group, a cycloalkyl group, a heterocyclic group, an alkenyl group, a cycloalkenyl group, an alkynyl group, a hydroxyl group, a thiol group, an alkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, an aryl group, a heteroaryl group, a halogen, a cyano group, an aldehyde group, a carbonyl group, a carboxyl group, an oxycarbonyl group, a carbamoyl group, an amino group, a nitro group, a silyl group, a siloxanyl group, a boryl group, a phosphine oxide group, and a fused ring and an aliphatic ring each formed between adjacent substituents).

13. The color conversion composition according to claim 7 , wherein the luminescent material (b) is a compound represented by the formula (1):

(wherein X is C—R 7 or N, and each of R 1 to R 9 , which may be the same as or different from one another, is selected from hydrogen, an alkyl group, a cycloalkyl group, a heterocyclic group, an alkenyl group, a cycloalkenyl group, an alkynyl group, a hydroxyl group, a thiol group, an alkoxy group, an alkylthio group, an aryl ether group, an aryl thioether group, an aryl group, a heteroaryl group, a halogen, a cyano group, an aldehyde group, a carbonyl group, a carboxyl group, an oxycarbonyl group, a carbamoyl group, an amino group, a nitro group, a silyl group, a siloxanyl group, a boryl group, a phosphine oxide group, and a fused ring and an aliphatic ring each formed between adjacent substituents).

14. The color conversion composition according to claim 1 , wherein the binder resin is a thermosetting resin.

15. A color conversion film comprising a layer obtained by curing the color conversion composition according to claim 1 .

16. The color conversion film according to claim 15 , which is coated with a gas barrier layer.

17. A light source unit comprising a light source and the color conversion film according to claim 15 .

18. The light source unit according to claim 17 , wherein the light source is a light-emitting diode having a maximum light emission in the range of 430 to 500 nm.

19. A display comprising the light source unit according to claim 17 .

20. A lighting comprising the light source unit according to claim 17 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2018
From: SAKAINO, HIROTOSHI; TANAKA, DAISAKU
To: TORAY INDUSTRIES, INC.
Reel/Frame 044638/0840 →
Priority Claims (2)
JP 2015-142696 · Jul 17, 2015 · national
JP 2015-142697 · Jul 17, 2015 · national
Continuity (1)
Related Publication 20180208838A1 · Jul 26, 2018