JPS635093A - ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法 - Google Patents

ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法

Info

Publication number: JPS635093A
Authority: JP; Japan
Prior art keywords: bis; naphthalocyanine; formula; layer; silicon
Prior art date: 1986-06-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

JP15012686A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0212954B2 (fr

Inventor

Shigeru Hayashida

茂林田

Seiji Tai

誠司田井

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Resonac Corp

Original Assignee

Hitachi Chemical Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-06-26

Filing date

1986-06-26

Publication date

1988-01-11

1986-06-26 Application filed by Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd

1986-06-26 Priority to JP15012686A priority Critical patent/JPS635093A/ja

1987-04-23 Priority to US07/041,409 priority patent/US4749637A/en

1987-04-24 Priority to DE8787303655T priority patent/DE3767752D1/de

1987-04-24 Priority to DE3789243T priority patent/DE3789243T2/de

1987-04-24 Priority to EP89122030A priority patent/EP0375967B1/fr

1987-04-24 Priority to EP87303655A priority patent/EP0243205B1/fr

1988-01-11 Publication of JPS635093A publication Critical patent/JPS635093A/ja

1989-05-03 Priority to US07/348,128 priority patent/US5081236A/en

1990-03-30 Publication of JPH0212954B2 publication Critical patent/JPH0212954B2/ja

1993-06-10 Priority to US08/074,975 priority patent/US5428152A/en

Status Granted legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title claims description 7
229920001296 polysiloxane Polymers 0.000 title description 5
239000000126 substance Substances 0.000 claims abstract description 9
125000000217 alkyl group Chemical group 0.000 claims abstract description 5
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
150000002367 halogens Chemical class 0.000 claims abstract description 5
LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 claims description 52
229910052710 silicon Inorganic materials 0.000 claims description 28
239000010703 silicon Substances 0.000 claims description 28
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 26
JHKWXZZEBNEOAE-UHFFFAOYSA-N dihydroxysilicon Chemical compound O[Si]O JHKWXZZEBNEOAE-UHFFFAOYSA-N 0.000 claims description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000005389 trialkylsiloxy group Chemical group 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
239000000463 material Substances 0.000 abstract description 14
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 abstract description 12
150000001875 compounds Chemical class 0.000 abstract description 9
-1 triethylsilanol Chemical class 0.000 abstract description 9
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract description 8
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 abstract description 6
230000003287 optical effect Effects 0.000 abstract description 3
239000003960 organic solvent Substances 0.000 abstract description 2
WVMSIBFANXCZKT-UHFFFAOYSA-N triethyl(hydroxy)silane Chemical compound CC[Si](O)(CC)CC WVMSIBFANXCZKT-UHFFFAOYSA-N 0.000 abstract description 2
239000003054 catalyst Substances 0.000 abstract 1
239000010410 layer Substances 0.000 description 29
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 28
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
239000013078 crystal Substances 0.000 description 14
239000000243 solution Substances 0.000 description 13
239000002904 solvent Substances 0.000 description 11
229910052751 metal Inorganic materials 0.000 description 10
239000002184 metal Substances 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
238000001816 cooling Methods 0.000 description 9
239000000203 mixture Substances 0.000 description 9
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
238000001720 action spectrum Methods 0.000 description 8
238000000034 method Methods 0.000 description 8
239000002244 precipitate Substances 0.000 description 8
239000011541 reaction mixture Substances 0.000 description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 7
239000010408 film Substances 0.000 description 7
230000008018 melting Effects 0.000 description 7
238000002844 melting Methods 0.000 description 7
238000002211 ultraviolet spectrum Methods 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000005259 measurement Methods 0.000 description 6
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 6
229920000620 organic polymer Polymers 0.000 description 6
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
239000000725 suspension Substances 0.000 description 6
ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 5
238000004458 analytical method Methods 0.000 description 5
239000007787 solid Substances 0.000 description 5
238000001228 spectrum Methods 0.000 description 5
239000010409 thin film Substances 0.000 description 5
238000001771 vacuum deposition Methods 0.000 description 5
239000011230 binding agent Substances 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
230000001965 increasing effect Effects 0.000 description 4
239000000047 product Substances 0.000 description 4
239000011241 protective layer Substances 0.000 description 4
238000001953 recrystallisation Methods 0.000 description 4
238000003756 stirring Methods 0.000 description 4
239000000758 substrate Substances 0.000 description 4
238000007738 vacuum evaporation Methods 0.000 description 4
239000008096 xylene Substances 0.000 description 4
JAWNWEKHDFBPSG-UHFFFAOYSA-N 3-iminobenzo[f]isoindol-1-amine Chemical compound C1=CC=C2C=C3C(N)=NC(=N)C3=CC2=C1 JAWNWEKHDFBPSG-UHFFFAOYSA-N 0.000 description 3
YCXNBETUNFJYPL-UHFFFAOYSA-N C(C)[Si](O[Si]O[Si](CC)(CC)CC)(CC)CC Chemical compound C(C)[Si](O[Si]O[Si](CC)(CC)CC)(CC)CC YCXNBETUNFJYPL-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
239000004020 conductor Substances 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
238000000921 elemental analysis Methods 0.000 description 3
150000002739 metals Chemical class 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
239000004800 polyvinyl chloride Substances 0.000 description 3
229920000915 polyvinyl chloride Polymers 0.000 description 3
239000002356 single layer Substances 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
ZNKCKMJPPQPCDT-UHFFFAOYSA-N CCC[Si](CCC)(CCC)O[Si]O[Si](CCC)(CCC)CCC Chemical compound CCC[Si](CCC)(CCC)O[Si]O[Si](CCC)(CCC)CCC ZNKCKMJPPQPCDT-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
239000003849 aromatic solvent Substances 0.000 description 2
MJVASWARXKAZOC-UHFFFAOYSA-N bis(trihexylsilyloxy)silicon Chemical compound CCCCCC[Si](CCCCCC)(CCCCCC)O[Si]O[Si](CCCCCC)(CCCCCC)CCCCCC MJVASWARXKAZOC-UHFFFAOYSA-N 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
229920002301 cellulose acetate Polymers 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
238000004440 column chromatography Methods 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
238000000151 deposition Methods 0.000 description 2
230000008021 deposition Effects 0.000 description 2
BUMGIEFFCMBQDG-UHFFFAOYSA-N dichlorosilicon Chemical class Cl[Si]Cl BUMGIEFFCMBQDG-UHFFFAOYSA-N 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
239000010931 gold Substances 0.000 description 2
GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 2
239000011133 lead Substances 0.000 description 2
239000012046 mixed solvent Substances 0.000 description 2
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000004926 polymethyl methacrylate Substances 0.000 description 2
229920002223 polystyrene Polymers 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000004065 semiconductor Substances 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
239000005049 silicon tetrachloride Substances 0.000 description 2
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
235000009518 sodium iodide Nutrition 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
238000006418 Brown reaction Methods 0.000 description 1
101150023090 CAH gene Proteins 0.000 description 1
108700018454 CDC15 Proteins 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241000219122 Cucurbita Species 0.000 description 1
235000009852 Cucurbita pepo Nutrition 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
206010034972 Photosensitivity reaction Diseases 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
229920001328 Polyvinylidene chloride Polymers 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000000956 alloy Substances 0.000 description 1
229910045601 alloy Inorganic materials 0.000 description 1
229910021417 amorphous silicon Inorganic materials 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
VNWTULBIIFEUNE-UHFFFAOYSA-N bis(tributylsilyloxy)silicon Chemical compound CCCC[Si](CCCC)(CCCC)O[Si]O[Si](CCCC)(CCCC)CCCC VNWTULBIIFEUNE-UHFFFAOYSA-N 0.000 description 1
QUSIXTNHZHDRQZ-UHFFFAOYSA-N bis(trimethylsilyloxy)silicon Chemical compound C[Si](C)(C)O[Si]O[Si](C)(C)C QUSIXTNHZHDRQZ-UHFFFAOYSA-N 0.000 description 1
230000005587 bubbling Effects 0.000 description 1
QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
150000001716 carbazoles Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
101150081467 cdc15 gene Proteins 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
ACTAPAGNZPZLEF-UHFFFAOYSA-N chloro(tripropyl)silane Chemical compound CCC[Si](Cl)(CCC)CCC ACTAPAGNZPZLEF-UHFFFAOYSA-N 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000003963 dichloro group Chemical group Cl* 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
238000003618 dip coating Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003480 eluent Substances 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
229920001973 fluoroelastomer Polymers 0.000 description 1
230000004907 flux Effects 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
RBBOWEDMXHTEPA-UHFFFAOYSA-N hexane;toluene Chemical compound CCCCCC.CC1=CC=CC=C1 RBBOWEDMXHTEPA-UHFFFAOYSA-N 0.000 description 1
150000007857 hydrazones Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000012535 impurity Substances 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
238000002955 isolation Methods 0.000 description 1
238000010030 laminating Methods 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000012528 membrane Substances 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000012452 mother liquor Substances 0.000 description 1
DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
KNBYJRSSFXTESR-UHFFFAOYSA-N naphthalene-2,3-dicarbonitrile Chemical compound C1=CC=C2C=C(C#N)C(C#N)=CC2=C1 KNBYJRSSFXTESR-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
239000011368 organic material Substances 0.000 description 1
150000004866 oxadiazoles Chemical class 0.000 description 1
150000007978 oxazole derivatives Chemical class 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
108091008695 photoreceptors Proteins 0.000 description 1
230000036211 photosensitivity Effects 0.000 description 1
230000002319 phototactic effect Effects 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
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 1
229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920005668 polycarbonate resin Polymers 0.000 description 1
239000004431 polycarbonate resin Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920001470 polyketone Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000003219 pyrazolines Chemical class 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001454 recorded image Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
238000004528 spin coating Methods 0.000 description 1
238000004544 sputter deposition Methods 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
238000003852 thin film production method Methods 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
ISEIIPDWJVGTQS-UHFFFAOYSA-N tributylsilicon Chemical compound CCCC[Si](CCCC)CCCC ISEIIPDWJVGTQS-UHFFFAOYSA-N 0.000 description 1
239000005051 trimethylchlorosilane Substances 0.000 description 1
150000004961 triphenylmethanes Chemical class 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
239000010937 tungsten Substances 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Landscapes

Nitrogen Condensed Heterocyclic Rings (AREA)

JP15012686A 1986-04-24 1986-06-26 ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法 Granted JPS635093A (ja)

Priority Applications (8)

Application Number	Priority Date	Filing Date	Title
JP15012686A JPS635093A (ja)	1986-06-26	1986-06-26	ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法
US07/041,409 US4749637A (en)	1986-04-24	1987-04-23	Electrophotographic plate with silicon naphthalocyanine
DE8787303655T DE3767752D1 (en)	1986-04-24	1987-04-24	Elektrophotographische platte.
DE3789243T DE3789243T2 (de)	1986-04-24	1987-04-24	Naphthalocyaninverbindungen und Verfahren zu ihrer Herstellung.
EP89122030A EP0375967B1 (fr)	1986-04-24	1987-04-24	Composés de naphtalo-cyanines et procédé pour leur préparation
EP87303655A EP0243205B1 (fr)	1986-04-24	1987-04-24	Plaque électrophotographique
US07/348,128 US5081236A (en)	1986-04-24	1989-05-03	Electrophotographic plate containing naphthalocyanines which contain siloxy groups
US08/074,975 US5428152A (en)	1986-04-24	1993-06-10	Bis(trialkylsiloxy)silicon naphthalocyanine compounds wherein all the alkyl groups are the same and have 1-3 carbon atoms

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP15012686A JPS635093A (ja)	1986-06-26	1986-06-26	ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法

Publications (2)

Publication Number	Publication Date
JPS635093A true JPS635093A (ja)	1988-01-11
JPH0212954B2 JPH0212954B2 (fr)	1990-03-30

Family

ID=15490048

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP15012686A Granted JPS635093A (ja)	1986-04-24	1986-06-26	ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法

Country Status (1)

Country	Link
JP (1)	JPS635093A (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH02155690A (ja) *	1988-12-08	1990-06-14	Ricoh Co Ltd	強誘電性高分子光記録媒体
JP2008115557A (ja) *	2006-11-01	2008-05-22	Okumura Corp	トンネル掘削機
JP2008163624A (ja) *	2006-12-28	2008-07-17	Okumura Corp	トンネル掘削機とトンネル掘削方法
JP2008163625A (ja) *	2006-12-28	2008-07-17	Okumura Corp	トンネル掘削機とトンネル掘削方法
EP2644660A1 (fr)	2012-03-27	2013-10-02	Konica Minolta Business Technologies, Inc.	Procédé de production de colorant, composition colorante, toner, encre pour enregistrement à jet d'encre et filtre coloré
EP3396728A1 (fr)	2017-04-28	2018-10-31	Panasonic Intellectual Property Management Co., Ltd.	Derivés de naphthalocyanine comme élément de conversion photoélectrique

1986
- 1986-06-26 JP JP15012686A patent/JPS635093A/ja active Granted

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH02155690A (ja) *	1988-12-08	1990-06-14	Ricoh Co Ltd	強誘電性高分子光記録媒体
JP2008115557A (ja) *	2006-11-01	2008-05-22	Okumura Corp	トンネル掘削機
JP2008163624A (ja) *	2006-12-28	2008-07-17	Okumura Corp	トンネル掘削機とトンネル掘削方法
JP2008163625A (ja) *	2006-12-28	2008-07-17	Okumura Corp	トンネル掘削機とトンネル掘削方法
EP2644660A1 (fr)	2012-03-27	2013-10-02	Konica Minolta Business Technologies, Inc.	Procédé de production de colorant, composition colorante, toner, encre pour enregistrement à jet d'encre et filtre coloré
US9062225B2 (en)	2012-03-27	2015-06-23	Konica Minolta Business Technologies, Inc.	Production process for colorant, colorant composition, toner, ink for ink jet recording and color filter
EP3396728A1 (fr)	2017-04-28	2018-10-31	Panasonic Intellectual Property Management Co., Ltd.	Derivés de naphthalocyanine comme élément de conversion photoélectrique
US10297766B2 (en)	2017-04-28	2019-05-21	Panasonic Intellectual Property Management Co., Ltd.	Composition containing naphthalocyanine derivative, photoelectric conversion element containing the same, and imaging device

Also Published As

Publication number	Publication date
JPH0212954B2 (fr)	1990-03-30

Legal Events

Date	Code	Title	Description
2005-03-30	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
US5428152A (en)	1995-06-27	Bis(trialkylsiloxy)silicon naphthalocyanine compounds wherein all the alkyl groups are the same and have 1-3 carbon atoms
JPH02664A (ja)	1990-01-05	ナフタロシアニン誘導体及びその製造法並びにそれを用いた光学記録媒体及びその光学記録媒体の製造法
JPS63186251A (ja)	1988-08-01	金属ナフタロシアニン誘導体膜及び電子写真感光体
JPS635093A (ja)	1988-01-11	ビス（トリアルキルシロキシ）シリコンナフタロシアニン及びその製造法
Mysyk et al.	1997	Electron acceptors of the fluorene series. Part 6. 1 Synthesis of 4, 5-dinitro-9-X-fluorene-2, 7-disulfonic acid derivatives, their charge transfer complexes with anthracene and sensitization of photoconductivity of poly-N-(2, 3-epoxypropyl) carbazole
JPH02283768A (ja)	1990-11-21	ナフタロシアニン誘導体及びその製造法並びにそれを用いた光学記録媒体及びその光学記録媒体の製造法
EP0284369A2 (fr)	1988-09-28	5-ou 6-alkoxycarbonyl-2,3-dicyanonaphtalènes et leur procédé de préparation
JPH03136059A (ja)	1991-06-10	電子写真感光体
JPH01110986A (ja)	1989-04-27	光学記録媒体
US5041665A (en)	1991-08-20	Process for preparing squarylium compounds
JPH07107138B2 (ja)	1995-11-15	ゲルマニウムナフタロシアニン誘導体
JPH01217362A (ja)	1989-08-30	電子写真感光体
JPH0475262B2 (fr)	1992-11-30
JPH02169671A (ja)	1990-06-29	結晶型オキシチタニウムフタロシアニンおよびそれを含む電子写真感光体の製造方法
JPH02178358A (ja)	1990-07-11	新規なフタロシアニン化合物およびそれを用いた電子写真感光体
JPH0253431B2 (fr)	1990-11-16
JPH06506241A (ja)	1994-07-14	ポリケトメチン色素
TWI383896B (zh)	2013-02-01	Optical recording materials, chalcone compounds and metal complexes
JPH0360350B2 (fr)	1991-09-13
JPH03208057A (ja)	1991-09-11	電子写真用感光体
JPH046701B2 (fr)	1992-02-06
JPH0348948B2 (fr)	1991-07-26
JP2867520B2 (ja)	1999-03-08	電子写真用感光体
JPS60260545A (ja)	1985-12-23	新規なアニリン誘導体およびその製造方法
JPH0344587B2 (fr)	1991-07-08