CN102317377A - 近红外线吸收色素及近红外线屏蔽滤光片 - Google Patents
近红外线吸收色素及近红外线屏蔽滤光片 Download PDFInfo
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- CN102317377A CN102317377A CN2010800079691A CN201080007969A CN102317377A CN 102317377 A CN102317377 A CN 102317377A CN 2010800079691 A CN2010800079691 A CN 2010800079691A CN 201080007969 A CN201080007969 A CN 201080007969A CN 102317377 A CN102317377 A CN 102317377A
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/16—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing nitrogen
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B53/00—Quinone imides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
- C07C251/30—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having nitrogen atoms of imino groups quaternised
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/32—Radiation-absorbing paints
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/208—Filters for use with infrared or ultraviolet radiation, e.g. for separating visible light from infrared and/or ultraviolet radiation
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/223—Absorbing filters containing organic substances, e.g. dyes, inks or pigments
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Optical Filters (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
雾度 | |
实施例1 | 1.05 |
实施例2 | 1.24 |
比较例1 | 4.15 |
比较例2 | 0.94 |
Claims (21)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009037367 | 2009-02-20 | ||
JP2009-037367 | 2009-02-20 | ||
PCT/JP2010/052422 WO2010095676A1 (ja) | 2009-02-20 | 2010-02-18 | 近赤外線吸収色素および近赤外線遮断フィルター |
Publications (2)
Publication Number | Publication Date |
---|---|
CN102317377A true CN102317377A (zh) | 2012-01-11 |
CN102317377B CN102317377B (zh) | 2014-06-11 |
Family
ID=42633956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201080007969.1A Expired - Fee Related CN102317377B (zh) | 2009-02-20 | 2010-02-18 | 近红外线吸收色素及近红外线屏蔽滤光片 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20110315939A1 (zh) |
JP (1) | JP5596667B2 (zh) |
KR (1) | KR101709800B1 (zh) |
CN (1) | CN102317377B (zh) |
WO (1) | WO2010095676A1 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107533170A (zh) * | 2015-05-20 | 2018-01-02 | 富士胶片株式会社 | 红外线吸收组合物、红外线截止滤波器、层叠体、图案形成方法及固体成像元件 |
CN107533171A (zh) * | 2015-05-12 | 2018-01-02 | 旭硝子株式会社 | 光学滤波器以及摄像装置 |
CN114008494A (zh) * | 2019-06-20 | 2022-02-01 | Agc株式会社 | 滤光片、成像装置和光学传感器 |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20120115238A (ko) * | 2009-12-16 | 2012-10-17 | 닛뽕 카릿또 가부시키가이샤 | 근적외선 흡수 색소 및 근적외선 흡수 조성물 |
JP5701552B2 (ja) * | 2010-09-24 | 2015-04-15 | カーリットホールディングス株式会社 | 近赤外線吸収色素及び近赤外線遮断フィルター |
DE102010055902A1 (de) | 2010-12-23 | 2012-06-28 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
US10642087B2 (en) | 2014-05-23 | 2020-05-05 | Eyesafe, Llc | Light emission reducing compounds for electronic devices |
US10901125B2 (en) | 2014-05-23 | 2021-01-26 | Eyesafe, Llc | Light emission reducing compounds for electronic devices |
KR20180104727A (ko) * | 2016-02-02 | 2018-09-21 | 에이지씨 가부시키가이샤 | 근적외선 흡수 색소, 광학 필터 및 촬상 장치 |
US11810532B2 (en) | 2018-11-28 | 2023-11-07 | Eyesafe Inc. | Systems for monitoring and regulating harmful blue light exposure from digital devices |
US10955697B2 (en) | 2018-11-28 | 2021-03-23 | Eyesafe Inc. | Light emission modification |
US11592701B2 (en) | 2018-11-28 | 2023-02-28 | Eyesafe Inc. | Backlight unit with emission modification |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0624146A (ja) * | 1992-05-12 | 1994-02-01 | Canon Inc | 赤外吸収化合物及びそれを用いた光記録媒体 |
JPH083870A (ja) * | 1994-06-13 | 1996-01-09 | Japan Carlit Co Ltd:The | 赤外線吸収加工繊維製品及びその加工方法 |
JP2006137933A (ja) * | 2004-10-13 | 2006-06-01 | Toyo Ink Mfg Co Ltd | 近赤外線吸収性コーティング剤およびそれを用いてなる近赤外線吸収積層体 |
WO2007097368A1 (ja) * | 2006-02-22 | 2007-08-30 | Hitachi Maxell, Ltd | ジイモニウム塩化合物、およびこれ含む近赤外線吸収組成物、並びに近赤外線吸収フィルタ、ディスプレイ用前面板 |
WO2007145289A1 (ja) * | 2006-06-14 | 2007-12-21 | Hitachi Maxell, Ltd. | ジイモニウム塩化合物、およびこれを含む近赤外線吸収組成物、並びに近赤外線吸収フィルタ、ディスプレイ用前面板 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10180922A (ja) | 1996-12-25 | 1998-07-07 | Nippon Kayaku Co Ltd | 赤外線吸収体 |
JP3987240B2 (ja) | 1999-07-05 | 2007-10-03 | 三井化学株式会社 | 赤外光吸収膜およびその製造方法 |
JP2004361733A (ja) * | 2003-06-05 | 2004-12-24 | Mitsubishi Chemicals Corp | 光学フィルター |
JP2008009206A (ja) * | 2006-06-30 | 2008-01-17 | Fujifilm Corp | 近赤外吸収フィルター |
JP2010018773A (ja) * | 2008-06-12 | 2010-01-28 | Nippon Shokubai Co Ltd | 近赤外線吸収粘着剤組成物 |
-
2010
- 2010-02-18 CN CN201080007969.1A patent/CN102317377B/zh not_active Expired - Fee Related
- 2010-02-18 JP JP2011500642A patent/JP5596667B2/ja active Active
- 2010-02-18 KR KR1020117021582A patent/KR101709800B1/ko active IP Right Grant
- 2010-02-18 WO PCT/JP2010/052422 patent/WO2010095676A1/ja active Application Filing
- 2010-02-18 US US13/202,509 patent/US20110315939A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0624146A (ja) * | 1992-05-12 | 1994-02-01 | Canon Inc | 赤外吸収化合物及びそれを用いた光記録媒体 |
JPH083870A (ja) * | 1994-06-13 | 1996-01-09 | Japan Carlit Co Ltd:The | 赤外線吸収加工繊維製品及びその加工方法 |
JP2006137933A (ja) * | 2004-10-13 | 2006-06-01 | Toyo Ink Mfg Co Ltd | 近赤外線吸収性コーティング剤およびそれを用いてなる近赤外線吸収積層体 |
WO2007097368A1 (ja) * | 2006-02-22 | 2007-08-30 | Hitachi Maxell, Ltd | ジイモニウム塩化合物、およびこれ含む近赤外線吸収組成物、並びに近赤外線吸収フィルタ、ディスプレイ用前面板 |
WO2007145289A1 (ja) * | 2006-06-14 | 2007-12-21 | Hitachi Maxell, Ltd. | ジイモニウム塩化合物、およびこれを含む近赤外線吸収組成物、並びに近赤外線吸収フィルタ、ディスプレイ用前面板 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107533171A (zh) * | 2015-05-12 | 2018-01-02 | 旭硝子株式会社 | 光学滤波器以及摄像装置 |
CN107533171B (zh) * | 2015-05-12 | 2020-07-24 | Agc株式会社 | 光学滤波器以及摄像装置 |
CN107533170A (zh) * | 2015-05-20 | 2018-01-02 | 富士胶片株式会社 | 红外线吸收组合物、红外线截止滤波器、层叠体、图案形成方法及固体成像元件 |
US10598835B2 (en) | 2015-05-20 | 2020-03-24 | Fujifilm Corporation | Infrared absorbing composition, infrared cut filter, laminate, pattern forming method, solid image pickup element |
CN114008494A (zh) * | 2019-06-20 | 2022-02-01 | Agc株式会社 | 滤光片、成像装置和光学传感器 |
Also Published As
Publication number | Publication date |
---|---|
US20110315939A1 (en) | 2011-12-29 |
KR101709800B1 (ko) | 2017-02-23 |
WO2010095676A1 (ja) | 2010-08-26 |
JP5596667B2 (ja) | 2014-09-24 |
JPWO2010095676A1 (ja) | 2012-08-30 |
KR20110119799A (ko) | 2011-11-02 |
CN102317377B (zh) | 2014-06-11 |
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