JP5829641B2

JP5829641B2 - 近赤外線吸収性液状組成物、これを用いた近赤外線カットフィルタ及びその製造方法、並びに、カメラモジュール及びその製造方法

近赤外線吸収性液状組成物、これを用いた近赤外線カットフィルタ及びその製造方法、並びに、カメラモジュール及びその製造方法 Download PDF

Info

Publication number: JP5829641B2
Authority: JP; Japan
Prior art keywords: group; compound; liquid composition; infrared; substituent
Prior art date: 2012-05-08
Legal status : Expired - Fee Related

Application number

JP2013037239A

Other languages

English (en)

Japanese (ja)

Other versions

JP2013253224A (ja

Inventor

漢那　慎一

慎一漢那

星戊朴

誠一人見

Current Assignee

Fujifilm Corp

Original Assignee

Fujifilm Corp

Priority date

2012-05-08

Filing date

2013-02-27

Publication date

2015-12-09

2013-02-27 Application filed by Fujifilm Corp filed Critical Fujifilm Corp

2013-02-27 Priority to JP2013037239A priority Critical patent/JP5829641B2/ja

2013-05-06 Priority to TW102116112A priority patent/TW201345987A/zh

2013-05-07 Priority to PCT/JP2013/063613 priority patent/WO2013168824A1/en

2013-05-07 Priority to CN201380024372.1A priority patent/CN104272146A/zh

2013-05-07 Priority to KR20147032280A priority patent/KR20150003830A/ko

2013-12-19 Publication of JP2013253224A publication Critical patent/JP2013253224A/ja

2015-12-09 Application granted granted Critical

2015-12-09 Publication of JP5829641B2 publication Critical patent/JP5829641B2/ja

Status Expired - Fee Related legal-status Critical Current

2033-02-27 Anticipated expiration legal-status Critical

Links

239000000203 mixture Substances 0.000 title claims description 115
239000007788 liquid Substances 0.000 title claims description 79
238000004519 manufacturing process Methods 0.000 title claims description 21
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IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
125000004953 trihalomethyl group Chemical group 0.000 description 1
FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 description 1
RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 1
238000000870 ultraviolet spectroscopy Methods 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1
238000007740 vapor deposition Methods 0.000 description 1
KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1