JP5785623B2 - ジイモニウム系化合物およびこれを利用した近赤外線吸収フィルター - Google Patents
ジイモニウム系化合物およびこれを利用した近赤外線吸収フィルター Download PDFInfo
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- 150000001875 compounds Chemical class 0.000 title claims description 42
- 238000010521 absorption reaction Methods 0.000 title claims description 19
- 239000000126 substance Substances 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 33
- -1 halogen ions Chemical class 0.000 description 21
- 239000000463 material Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 12
- 239000011358 absorbing material Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 9
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 8
- 230000031700 light absorption Effects 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000001153 fluoro group Chemical group F* 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- INGVZLYSYVSTRR-UHFFFAOYSA-N 4-n-[4-[4-[bis(2-methylpropyl)amino]-n-[4-[bis(2-methylpropyl)amino]phenyl]anilino]phenyl]-4-n-[4-[bis(2-methylpropyl)amino]phenyl]-1-n,1-n-bis(2-methylpropyl)benzene-1,4-diamine Chemical compound C1=CC(N(CC(C)C)CC(C)C)=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC(=CC=1)N(CC(C)C)CC(C)C)C=1C=CC(=CC=1)N(CC(C)C)CC(C)C)C1=CC=C(N(CC(C)C)CC(C)C)C=C1 INGVZLYSYVSTRR-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- YRZZLAGRKZIJJI-UHFFFAOYSA-N oxyvanadium phthalocyanine Chemical compound [V+2]=O.C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 YRZZLAGRKZIJJI-UHFFFAOYSA-N 0.000 description 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000002952 polymeric resin Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 150000004662 dithiols Chemical class 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 235000003270 potassium fluoride Nutrition 0.000 description 2
- 239000011698 potassium fluoride Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 2
- HLVFKOKELQSXIQ-UHFFFAOYSA-N 1-bromo-2-methylpropane Chemical compound CC(C)CBr HLVFKOKELQSXIQ-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- OFLRJMBSWDXSPG-UHFFFAOYSA-N 3,4,5,6-tetrafluorobenzene-1,2-dicarbonitrile Chemical compound FC1=C(F)C(F)=C(C#N)C(C#N)=C1F OFLRJMBSWDXSPG-UHFFFAOYSA-N 0.000 description 1
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- IYOMQTGPEVJQDR-UHFFFAOYSA-N B([O-])(O)O.[Li+].C(CC(=O)O)(=O)O.C(CC(=O)O)(=O)O Chemical compound B([O-])(O)O.[Li+].C(CC(=O)O)(=O)O.C(CC(=O)O)(=O)O IYOMQTGPEVJQDR-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910021551 Vanadium(III) chloride Inorganic materials 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229940125773 compound 10 Drugs 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- DEUISMFZZMAAOJ-UHFFFAOYSA-N lithium dihydrogen borate oxalic acid Chemical compound B([O-])(O)O.C(C(=O)O)(=O)O.C(C(=O)O)(=O)O.[Li+] DEUISMFZZMAAOJ-UHFFFAOYSA-N 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001692 polycarbonate urethane Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- HQYCOEXWFMFWLR-UHFFFAOYSA-K vanadium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[V+3] HQYCOEXWFMFWLR-UHFFFAOYSA-K 0.000 description 1
- 125000005287 vanadyl group Chemical group 0.000 description 1
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids
-
- 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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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Optical Filters (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
上記化学式1で、R1ないしR8は、それぞれ独立的に、水素原子(H)、置換または非置換された炭素数1ないし10のアルキル基、又は、置換または非置換された炭素数6ないし14のアリール基であり、nは0または1である。
本発明によるジイモニウム系化合物は、下記の化学式1で表示される。
上記化学式1で、R1ないしR8は、それぞれ独立的に、水素原子(H)、置換または非置換された炭素数1ないし10、好ましくは炭素数1ないし6のアルキル基、置換または非置換された炭素数6ないし14、好ましくは6ないし10のアリール基、例えば、置換または非置換されたフェニル基であり、nは0または1である。ここで、前記R1ないしR8の置換基としては、炭素数1ないし5のアルキル基、フッ素を除くハロゲン基などを例示することができる。
還流装置が設けられた3口フラスコにN、N、N’、N’−テトラキス(4−アミノフェニル)−1、4−フェニレンジアミン12g、イソブチルブロマイド40gおよび重炭酸ナトリウム18gを入れ、N−メチルピロリドン30gを投入した後、混合物を80℃で9時間攪拌しながら反応させた。反応終了後、そのフラスコにジクロロメタン300gと水1Lを投入し、30分間攪拌した。攪拌終了後、層分離されたジクロロメタン層を真空蒸留器で蒸留して、N、N、N’、N’−テトラキス(p−ジイソブチルアミノフェニル)−p−フェニレンジアミン(粗反応物)30gを得た。
前記実施例1と同様な方法で得られたN、N、N’、N’−テトラキス(p−ジイソブチルアミノフェニル)−p−フェニレンジアミン30gとリチウムビスマロネートボレート15g、ジクロロメタン150gおよびイソブタノール60gを入れて2時間還流させた後、過硫酸ナトリウム10gと水200gを追加し、2時間還流させた。還流終了後、前記反応フラスコにジクロロメタン250gと水300gをさらに投入し、層分離されたジクロロメタン層を真空蒸留器で蒸留して、ジイモニウム系化合物であるビスマロネートボレートN、N、N’、N’−テトラキス(p−ジイソブチルアミノフェニル)−p−フェニレンジイモニウム(bis(malonato)borate N、N、N’、N’−tetrakis(p−diisobutylaminophenyl)−p−phenylenediimonium)8gを得た。
前記実施例1と同様な方法で得られたN、N、N’、N’−テトラキス(p−ジイソブチルアミノフェニル)−p−フェニレンジアミン30gとリチウムビストリフルオロメタンスルホニルイミド15g、ジクロロメタン150gおよびエタノール60gを入れて2時間還流させた後、過硫酸ナトリウム10gと水200gを追加し、2時間還流させた。還流終了後、前記反応フラスコにジクロロメタン250gと水300gをさらに投入し、層分離されたジクロロメタン層を真空蒸留器で蒸留して、ジイモニウム系化合物であるビストリフルオロメタンスルホニルイミドN、N、N’、N’−テトラキス(p−ジイソブチルアミノフェニル)−p−フェニレンジイモニウム(bistrifluoromethanesulfonylimide N、N、N’、N’−tetrakis(p−diisobutylaminophenyl)−p−phenylenediimonium)10gを得た。
還流装置が設けられた3口フラスコに3、4、5、6−テトラフルオロフタロニトリル10g、チオフェノール10gおよびフッ化カリウム7gを入れて、溶媒としてアセトニトリル30mlを投入した後、混合物を常温で12時間攪拌しながら反応させた。反応終了後、その反応液に2、6−ジメチルフェノール7gとフッ化カリウム4gを投入し、8時間還流させた。反応終了後、その溶液を真空蒸留器で蒸留した。このように得られた粗反応物20gを、還流装置が設けられた3口フラスコに入れ、バナジウムトリクロライド2g、1−オクタノール2gおよびベンゾニトリル30gと共に8時間還流させた。反応終了後、その溶液は真空蒸留器で蒸留され、バナジル(酸化バナジウム)フタロシアニン系(VOPc:Oxo−Vanadium Phthalocyanine)前駆体化合物VOPc(PhS)8{2、6−(CH3)2PhO}4F4を収得した。前記バナジルフタロシアニン系化合物前駆体10gとシクロヘキシルアミン50mlを、還流装置が設けられた3口フラスコに入れて、60℃で8時間反応させた。反応終了後、反応液を真空濃縮して、下記の化学式2で表示されるバナジルフタロシアニン化合物VOPc(PhS)8{2、6−(CH3)2PhO}4(C6H11NH)4(Ph=phenyl;下記の化学式2のA2、A3、A6、A7、A10、A11、A14およびA15がPhSであり;A1、A5、A9およびA13が{2、6−(CH3)2PhO}であり;A4、A8、A12およびA16がC6H11NHである)を得た。
前記実施例1、実施例2、比較例1および比較例2で製造されたジイモニウム系化合物およびバナジルフタロシアニン化合物を、トルエンにそれぞれ希釈し、UV/VISスペクトルを測定した。実施例1、実施例2および比較例1のジイモニウム系化合物の最大吸収波長は1000nm以上であり、比較例2のバナジルフタロシアニン化合物の最大吸収波長は932nmであった。また、実施例1、比較例1および比較例2で製造されたジイモニウム系化合物およびバナジルフタロシアニン化合物のUV/VIS吸収スペクトルを図1に示す。
Claims (2)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20100136942A KR101251898B1 (ko) | 2010-12-28 | 2010-12-28 | 디이모늄계 화합물 및 이를 이용한 근적외선 흡수 필터 |
KR10-2010-0136942 | 2010-12-28 | ||
PCT/KR2011/010082 WO2012091379A2 (ko) | 2010-12-28 | 2011-12-26 | 디이모늄계 화합물 및 이를 이용한 근적외선 흡수 필터 |
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JP2014506252A JP2014506252A (ja) | 2014-03-13 |
JP5785623B2 true JP5785623B2 (ja) | 2015-09-30 |
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JP (1) | JP5785623B2 (ja) |
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TWI711535B (zh) | 2018-10-31 | 2020-12-01 | 竹內忍 | 進行板材加工的加工裝置及加工方法 |
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KR101653865B1 (ko) * | 2013-06-18 | 2016-09-02 | 주식회사 엘지화학 | 염료 및 이를 포함하는 컬러필터 |
CN107430226B (zh) * | 2015-03-17 | 2020-08-25 | 株式会社Lms | 滤光器及包括其的成像装置 |
US10969526B2 (en) * | 2017-09-08 | 2021-04-06 | Apple Inc. | Coatings for transparent substrates in electronic devices |
KR102449992B1 (ko) * | 2018-12-10 | 2022-10-05 | 연세대학교 산학협력단 | 퀴노이드계 이온화합물, 이의 제조방법, 상기 퀴노이드계 이온화합물을 포함하는 투명한 근적외선 차단막 및 이의 제조방법 |
WO2021085372A1 (ja) | 2019-11-01 | 2021-05-06 | Jsr株式会社 | 樹脂組成物、化合物(z)、光学フィルターおよびその用途 |
KR102575190B1 (ko) * | 2022-11-21 | 2023-09-06 | 한국화학연구원 | 근적외선 흡수제 및 이를 포함하는 근적외선 차단 필터 |
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JP3278010B2 (ja) * | 1993-09-01 | 2002-04-30 | 凸版印刷株式会社 | 赤外線吸収インキ組成物 |
JPH09255890A (ja) * | 1996-03-22 | 1997-09-30 | Japan Carlit Co Ltd:The | 繊維染色用近赤外線吸収色素水分散液 |
EP1690905A1 (en) * | 2003-10-20 | 2006-08-16 | Sumitomo Osaka Cement Co., Ltd. | Near-infrared shielding paint, near-infrared shielding laminate obtained therefrom and process for producing the same |
CA2578107A1 (en) * | 2004-09-06 | 2006-03-16 | Nippon Kayaku Kabushiki Kaisha | Diimmonium compound and use thereof |
DE602006018707D1 (de) * | 2005-02-04 | 2011-01-20 | Nippon Catalytic Chem Ind | Borat und material, das strahlung im nahen infrarotbereich absorbiert |
KR20080007333A (ko) * | 2005-05-13 | 2008-01-18 | 니폰 가야꾸 가부시끼가이샤 | 디이모늄 화합물 및 그의 용도 |
JP4901248B2 (ja) * | 2006-03-17 | 2012-03-21 | 日本化薬株式会社 | ジイモニウム化合物及びその用途 |
KR100791931B1 (ko) * | 2006-09-06 | 2008-01-04 | 에스케이케미칼주식회사 | 디이모늄염 및 이를 포함하는 근적외선 흡수필름 |
JPWO2009001662A1 (ja) * | 2007-06-27 | 2010-08-26 | 日本化薬株式会社 | 近赤外線吸収フィルム及びこれを用いたプラズマディスプレイパネル用光学フィルタ |
DE102008021271A1 (de) | 2008-04-29 | 2010-01-28 | Merck Patent Gmbh | Reaktive ionische Flüssigkeiten |
US9176357B2 (en) * | 2010-12-15 | 2015-11-03 | Switch Materials, Inc. | Variable transmittance optical devices |
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TWI711535B (zh) | 2018-10-31 | 2020-12-01 | 竹內忍 | 進行板材加工的加工裝置及加工方法 |
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CN103270019B (zh) | 2016-02-03 |
JP2014506252A (ja) | 2014-03-13 |
WO2012091379A2 (ko) | 2012-07-05 |
US20130331608A1 (en) | 2013-12-12 |
KR20120074947A (ko) | 2012-07-06 |
WO2012091379A3 (ko) | 2012-09-27 |
US9158048B2 (en) | 2015-10-13 |
CN103270019A (zh) | 2013-08-28 |
KR101251898B1 (ko) | 2013-04-08 |
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