IP Library › Granted Patent US 10,947,389
Granted Patent B2
US 10,947,389 · App. 16/019,178 · Granted Mar 16, 2021

Composition, film, near infrared cut filter, laminate, pattern forming method, solid image pickup element, image display device, infrared sensor, and color filter

Inventors: Tokihiko Matsumura (Haibara-gun, JP); Daisuke Sasaki (Haibara-gun, JP); Kyohei Arayama (Haibara-gun, JP); Yoshihiro Jimbo (Haibara-gun, JP); Kazuya Oota (Haibara-gun, JP); Keisuke Arimura (Haibara-gun, JP); Takahiro Okawara (Haibara-gun, JP)
Assignee: FUJIFILM Corporation
C09B23/145C08F2/48C08F220/18C08K5/55C08L33/10C09B23/0008C09B23/0016C09B23/0025C09B23/0033C09B23/0041C09B23/0058C09B23/0066C09B23/0075C09B23/083C09B23/086C09B57/007C09B57/008G02B5/201G02B5/208G02B5/223G03F7/162G03F7/168G03F7/2004G03F7/322G03F7/38H01L27/14621H01L27/14649H01L27/14806H01L27/14875G03F7/0007G03F7/027G03F7/031G03F7/033G03F7/0751
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Quick Facts
Patent No.
US 10,947,389
App. No.
16/019,178
Granted
Mar 16, 2021
Kind
B2
Abstract

The composition includes two or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C., in which the two or more near infrared absorbing compounds include a first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, and a second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, and a difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm.

Claims (87)

1. A composition comprising:

two or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C.,

wherein the two or more near infrared absorbing compounds include

a first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, and

a second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, and

a difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm,

wherein both the first near infrared absorbing compound and the second near infrared absorbing compound are compounds represented by the following Formula (SQ-1),

in Formula (SQ-1), a ring A and a ring B each independently represent an aromatic ring,

X A and X B each independently represent a substituent,

G A and G B each independently represent a substituent,

kA represents an integer of 0 to nA, and kB represents an integer of 0 to nB,

nA represents an integer representing the maximum number of G A 's which may be substituted in the ring A, and nB represents an integer representing the maximum number of G B 's which may be substituted in the ring B,

X A and G A , or X B and G B may be bonded to each other to form a ring, and in a case where a plurality of G A 's and a plurality of G B 's are present, G A 's or G B 's may be bonded to each other to form a ring, and

wherein Formula (SQ-1) of at least one of the first near infrared absorbing compound or the second near infrared absorbing compound is a compound represented by the following Formula (SQ-A),

in Formula (SQ-A), R 1 and R 2 each independently represent an alkyl group, an alkenyl group, an aryl group, or a heteroaryl group,

R 3 and R 4 each independently represent a hydrogen atom or an alkyl group,

X 1 and X 2 each independently represent an oxygen atom or —N(R 5 )—,

R 5 represents a hydrogen atom, an alkyl group, an aryl group, or a heteroaryl group,

Y 1 to Y 4 each independently represent a substituent, and Y 1 and Y 2 or Y 3 and Y 4 may be bonded to each other to form a ring,

in a case where a plurality of Y 1 's, a plurality of Y 2 's, a plurality of Y 3 's, and a plurality of Y 4 's are present, Y 1 's, Y 2 's, Y 3 's, or Y 4 's may be bonded to each other to form a ring,

p and s each independently represent an integer of 0 to 3, and

q and r each independently represent an integer of 0 to 2.

2. The composition according to claim 1 ,

wherein in each of the first near infrared absorbing compound and the second near infrared absorbing compound, a ratio A1/A2 of an absorbance A1 at a wavelength of 500 nm to an absorbance A2 at the absorption maximum is 0.04 or lower.

3. The composition according to claim 1 ,

wherein a difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 90 nm.

4. The composition according to claim 1 , further comprising:

a curable compound;

a resin; and

a solvent.

5. The composition according to claim 1 , further comprising:

a chromatic colorant.

6. A film comprising:

the composition according to claim 1 .

7. A solid image pickup element comprising:

the film according to claim 6 .

8. An image display device comprising:

the film according to claim 6 .

9. An infrared sensor comprising:

the film according to claim 6 .

10. A near infrared cut filter comprising:

the composition according to claim 1 .

11. The near infrared cut filter according to claim 10 , further comprising:

a layer containing copper.

12. A laminate comprising:

the near infrared cut filter according to claim 11 ; and

a color filter that includes a chromatic colorant.

13. A pattern forming method comprising:

forming a composition layer on a support, the composition layer including the composition according to claim 1 ; and

forming a pattern on the composition layer using a photolithography method or a dry etching method.

14. A color filter comprising:

a pixel that includes the composition according to claim 1 ; and

a pixel selected from the group consisting of a red pixel, a green pixel, a blue pixel, a magenta pixel, a yellow pixel, a cyan pixel, a black pixel, and an achromatic pixel.

15. A composition comprising:

two or more near infrared absorbing compounds having an absorption maximum in a wavelength range of 650 to 1000 nm and having a solubility of 0.1 mass % or lower in water at 23° C.,

wherein the two or more near infrared absorbing compounds include

a first near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm, and

a second near infrared absorbing compound having an absorption maximum in a wavelength range of 650 to 1000 nm which is shorter than the absorption maximum of the first near infrared absorbing compound, and

a difference between the absorption maximum of the first near infrared absorbing compound and the absorption maximum of the second near infrared absorbing compound is 1 to 150 nm, and

wherein at least one of the first near infrared absorbing compound or the second near infrared absorbing compound includes a compound represented by the following Formula (I),

in Formula (I), A 1 and A 2 each independently represent a heteroaryl group,

B 1 and B 2 each independently represent a —BR 1 R 2 group,

R 1 and R 2 each independently represent a substituent,

It′ and R 2 may be bonded to each other to form a ring,

C 1 and C 2 each independently represent an alkyl group, an aryl group, or a heteroaryl group, and

D 1 and D 2 each independently represent a substituent.

16. The composition according to claim 15 ,

wherein Formula (I) is represented by the following Formula (II) or the following Formula (III),

in Formula (II), X 1 and X 2 each independently represent 0, S, NR X1 , or CR X2 R X3 ,

R X1 to R X3 each independently represent a hydrogen atom or a substituent,

R 3 to R 6 each independently represent a hydrogen atom or a substituent,

R 3 and R 4 , or R 5 and R 6 may be bonded to form a ring,

B 1 and B 2 each independently represent a —BR 1 R 2 group,

R 1 and R 2 each independently represent a substituent,

R 1 and R 2 may be bonded to each other to form a ring,

C 1 and C 2 each independently represent an alkyl group, an aryl group, or a heteroaryl group, and

D 1 and D 2 each independently represent a substituent,

in Formula (III), Y 1 to Y 8 each independently represent N or CR Y1 ,

at least two of Y 1 , Y 2 , Y 3 , or Y 4 represent CR Y1 ,

at least two of Y 5 , Y 6 , Y 7 , or Y 8 represent CR Y1 ,

R Y1 represents a hydrogen atom or a substituent,

adjacent R Y1 's may be bonded to each other to form a ring,

B 1 and B 2 each independently represent a —BR 1 R 2 group,

R 1 and R 2 each independently represent a substituent,

R 1 and R 2 may be bonded to each other to form a ring,

C 1 and C 2 each independently represent an alkyl group, an aryl group, or a heteroaryl group, and

D 1 and D 2 each independently represent a substituent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2018
From: MATSUMURA, TOKIHIKO; SASAKI, DAISUKE; ARAYAMA, KYOHEI; JIMBO, YOSHIHIRO; OOTA, KAZUYA; ARIMURA, KEISUKE; OKAWARA, TAKAHIRO
To: FUJIFILM CORPORATION
Reel/Frame 046233/0390 →
Priority Claims (3)
JP JP2016-015782 · Jan 29, 2016 · national
JP JP2016-142116 · Jul 20, 2016 · national
JP JP2016-228784 · Nov 25, 2016 · national
Continuity (2)
Continuation PCTJP2017001678 · Jan 19, 2017
Related Publication 20180305552A1 · Oct 25, 2018