JPS6044390A - 光記録媒体 - Google Patents

光記録媒体

Info

Publication number: JPS6044390A
Authority: JP; Japan
Prior art keywords: group; ring; general formula; dye; resin
Prior art date: 1983-08-23
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

JP58153393A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0475146B2 (fr

Inventor

Noriyoshi Nanba

憲良南波

Shigeru Asami

浅見　茂

Toshiki Aoi

利樹青井

Kazuo Takahashi

一夫高橋

Akihiko Kuroiwa

黒岩　顕彦

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.)

TDK Corp

Original Assignee

TDK Corp

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.)

1983-08-23

Filing date

1983-08-23

Publication date

1985-03-09

1983-08-23 Application filed by TDK Corp filed Critical TDK Corp

1983-08-23 Priority to JP58153393A priority Critical patent/JPS6044390A/ja

1985-03-09 Publication of JPS6044390A publication Critical patent/JPS6044390A/ja

1992-11-30 Publication of JPH0475146B2 publication Critical patent/JPH0475146B2/ja

Status Granted legal-status Critical Current

Links

230000003287 optical effect Effects 0.000 title claims description 14
125000000217 alkyl group Chemical group 0.000 claims abstract description 30
125000003118 aryl group Chemical group 0.000 claims abstract description 27
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 18
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 9
150000001450 anions Chemical class 0.000 claims abstract description 3
125000005647 linker group Chemical group 0.000 claims abstract description 3
229920005989 resin Polymers 0.000 claims description 30
239000011347 resin Substances 0.000 claims description 30
229920000642 polymer Polymers 0.000 claims description 18
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
125000001041 indolyl group Chemical group 0.000 claims description 5
229910052751 metal Inorganic materials 0.000 claims description 5
239000002184 metal Substances 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 4
125000000547 substituted alkyl group Chemical group 0.000 claims description 4
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
229910052737 gold Inorganic materials 0.000 claims description 2
239000010931 gold Substances 0.000 claims description 2
125000002883 imidazolyl group Chemical group 0.000 claims description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 1
125000002971 oxazolyl group Chemical group 0.000 claims 1
230000007704 transition Effects 0.000 claims 1
230000006866 deterioration Effects 0.000 abstract description 6
229920005992 thermoplastic resin Polymers 0.000 abstract description 4
150000003624 transition metals Chemical group 0.000 abstract 1
PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 38
239000000975 dye Substances 0.000 description 33
229920001577 copolymer Polymers 0.000 description 32
239000010410 layer Substances 0.000 description 29
-1 halogen radical Chemical class 0.000 description 22
125000004432 carbon atom Chemical group C* 0.000 description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
125000001424 substituent group Chemical group 0.000 description 10
239000000758 substrate Substances 0.000 description 9
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 8
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
239000004677 Nylon Substances 0.000 description 6
239000002253 acid Substances 0.000 description 6
125000002252 acyl group Chemical group 0.000 description 6
125000000623 heterocyclic group Chemical group 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
229920001778 nylon Polymers 0.000 description 6
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 5
125000003545 alkoxy group Chemical group 0.000 description 5
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 5
238000007334 copolymerization reaction Methods 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 5
239000010936 titanium Substances 0.000 description 5
229910052719 titanium Inorganic materials 0.000 description 5
229920002554 vinyl polymer Polymers 0.000 description 5
239000004925 Acrylic resin Substances 0.000 description 4
229920000178 Acrylic resin Polymers 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
239000000020 Nitrocellulose Substances 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
125000004453 alkoxycarbonyl group Chemical group 0.000 description 4
229910052782 aluminium Inorganic materials 0.000 description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 4
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
239000011248 coating agent Substances 0.000 description 4
238000000576 coating method Methods 0.000 description 4
238000009833 condensation Methods 0.000 description 4
230000005494 condensation Effects 0.000 description 4
150000002334 glycols Chemical class 0.000 description 4
229920001220 nitrocellulos Polymers 0.000 description 4
125000004433 nitrogen atom Chemical group N* 0.000 description 4
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
229920002292 Nylon 6 Polymers 0.000 description 3
229920002302 Nylon 6,6 Polymers 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
125000004442 acylamino group Chemical group 0.000 description 3
125000003282 alkyl amino group Chemical group 0.000 description 3
125000003710 aryl alkyl group Chemical group 0.000 description 3
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 3
239000003431 cross linking reagent Substances 0.000 description 3
125000000753 cycloalkyl group Chemical group 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
125000005843 halogen group Chemical group 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 3
229920005749 polyurethane resin Polymers 0.000 description 3
125000006850 spacer group Chemical group 0.000 description 3
238000005809 transesterification reaction Methods 0.000 description 3
229910052845 zircon Inorganic materials 0.000 description 3
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 3
GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
101000798993 Pseudomonas putida (strain ATCC 700007 / DSM 6899 / BCRC 17059 / F1) 2-hydroxy-6-oxo-2,4-heptadienoate hydrolase Proteins 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
125000004423 acyloxy group Chemical group 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000004703 alkoxides Chemical class 0.000 description 2
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 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
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 2
125000004391 aryl sulfonyl group Chemical group 0.000 description 2
238000006065 biodegradation reaction Methods 0.000 description 2
230000008033 biological extinction Effects 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
235000010980 cellulose Nutrition 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 2
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical group OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000000155 melt Substances 0.000 description 2
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125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 description 2
150000003505 terpenes Chemical class 0.000 description 2
235000007586 terpenes Nutrition 0.000 description 2
229910052723 transition metal Inorganic materials 0.000 description 2
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229940117958 vinyl acetate Drugs 0.000 description 2
WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
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VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
235000017788 Cydonia oblonga Nutrition 0.000 description 1
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241000907681 Morpho Species 0.000 description 1
101100450563 Mus musculus Serpind1 gene Proteins 0.000 description 1
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229920000299 Nylon 12 Polymers 0.000 description 1
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239000004698 Polyethylene Substances 0.000 description 1
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239000004372 Polyvinyl alcohol Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
101000650578 Salmonella phage P22 Regulatory protein C3 Proteins 0.000 description 1
239000002262 Schiff base Substances 0.000 description 1
150000004753 Schiff bases Chemical class 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
239000002174 Styrene-butadiene Substances 0.000 description 1
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101001040920 Triticum aestivum Alpha-amylase inhibitor 0.28 Proteins 0.000 description 1
102100024063 Type I iodothyronine deiodinase Human genes 0.000 description 1
101710119122 Type I iodothyronine deiodinase Proteins 0.000 description 1
241000545067 Venus Species 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 1
229940081735 acetylcellulose Drugs 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
229920006322 acrylamide copolymer Polymers 0.000 description 1
125000005396 acrylic acid ester group Chemical group 0.000 description 1
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
229920001893 acrylonitrile styrene Polymers 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
125000005153 alkyl sulfamoyl group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
125000005116 aryl carbamoyl group Chemical group 0.000 description 1
125000004657 aryl sulfonyl amino group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
229930006722 beta-pinene Natural products 0.000 description 1
210000000941 bile Anatomy 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
235000021152 breakfast Nutrition 0.000 description 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
125000005586 carbonic acid group Chemical group 0.000 description 1
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
GRFFKYTUNTWAGG-UHFFFAOYSA-N chloroethene;prop-2-enenitrile Chemical compound ClC=C.C=CC#N GRFFKYTUNTWAGG-UHFFFAOYSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
IBAHLNWTOIHLKE-UHFFFAOYSA-N cyano cyanate Chemical class N#COC#N IBAHLNWTOIHLKE-UHFFFAOYSA-N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
150000003997 cyclic ketones Chemical class 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
125000006639 cyclohexyl carbonyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
230000002542 deteriorative effect Effects 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
150000002085 enols Chemical class 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229920001249 ethyl cellulose Polymers 0.000 description 1
235000019325 ethyl cellulose Nutrition 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
229920006226 ethylene-acrylic acid Polymers 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000012634 fragment Substances 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
238000005338 heat storage Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000001863 hydroxypropyl cellulose Substances 0.000 description 1
235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
229920000554 ionomer Polymers 0.000 description 1
GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
230000031700 light absorption Effects 0.000 description 1
235000001510 limonene Nutrition 0.000 description 1
229940087305 limonene Drugs 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
238000000034 method Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
CELWCAITJAEQNL-UHFFFAOYSA-N oxan-2-ol Chemical group OC1CCCCO1 CELWCAITJAEQNL-UHFFFAOYSA-N 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical group C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
230000027870 phototropism Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
239000004431 polycarbonate resin Substances 0.000 description 1
229920005668 polycarbonate resin Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920006380 polyphenylene oxide Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920001289 polyvinyl ether Polymers 0.000 description 1
SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
125000005493 quinolyl group Chemical group 0.000 description 1
GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
238000012827 research and development Methods 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
125000004149 thio group Chemical group *S* 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
- G11B7/247—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes
- G11B7/2472—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes cyanine
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/249—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing organometallic compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Thermal Transfer Or Thermal Recording In General (AREA)
Optical Record Carriers And Manufacture Thereof (AREA)

JP58153393A 1983-08-23 1983-08-23 光記録媒体 Granted JPS6044390A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP58153393A JPS6044390A (ja)	1983-08-23	1983-08-23	光記録媒体

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP58153393A JPS6044390A (ja)	1983-08-23	1983-08-23	光記録媒体

Publications (2)

Publication Number	Publication Date
JPS6044390A true JPS6044390A (ja)	1985-03-09
JPH0475146B2 JPH0475146B2 (fr)	1992-11-30

Family

ID=15561505

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP58153393A Granted JPS6044390A (ja)	1983-08-23	1983-08-23	光記録媒体

Country Status (1)

Country	Link
JP (1)	JPS6044390A (fr)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6440389A (en) *	1987-08-06	1989-02-10	Taiyo Yuden Kk	Optical data recording medium
US5330542A (en) *	1990-05-25	1994-07-19	Mitsubishi Kasei Corporation	Dye-incorporated composition
EP0597826A3 (fr) *	1987-08-05	1995-08-30	Canon Kk	Support d'enregistrement de données.
WO2003042989A1 (fr) *	2001-11-13	2003-05-22	Ciba Specialty Chemicals Holding Inc.	Compositions comprenant au moins un colorant a base d'oxonol et au moins un complexe metallique
WO2004102551A3 (fr) *	2003-05-14	2005-03-31	Ciba Sc Holding Ag	Nouveaux metaux complexes
WO2007119672A1 (fr)	2006-04-10	2007-10-25	Fujifilm Corporation	Support d'enregistrement optique, procédé d'enregistrement d'informations visibles et utilisation d'un colorant
WO2008108406A1 (fr)	2007-03-05	2008-09-12	Fujifilm Corporation	Composé pour résine photosensible, solution de résine photosensible, et procédé de gravure utilisant la solution de résine photosensible
WO2008123010A1 (fr)	2007-03-05	2008-10-16	Fujifilm Corporation	Elément électroluminescent, procédé de fabrication de l'élément électroluminescent, élément optique et procédé de fabrication de l'élément optique
EP1998329A2 (fr)	2007-06-01	2008-12-03	Fujifilm Corporation	Support d'enregistrement d'informations optiques et procédé d'enregistrement d'informations
WO2009022442A1 (fr)	2007-08-16	2009-02-19	Fujifilm Corporation	Procédé pour fabriquer un support sur lequel des informations sont enregistrées par un motif de cuvette
WO2009050858A1 (fr)	2007-10-15	2009-04-23	Fujifilm Corporation	Procédé de nettoyage d'une couche de support d'enregistrement de type en mode thermique, procédé de fabrication d'un produit comportant des creux et des saillies, procédé de fabrication d'un élément électroluminescent et procédé de fabrication d'un élément optique
WO2009110046A1 (fr)	2008-03-05	2009-09-11	富士フイルム株式会社	Procédé de traitement d'une pièce de travail ayant une couche photosensible
WO2009113272A1 (fr)	2008-03-10	2009-09-17	富士フイルム株式会社	Procédé de traitement de moule et procédé de fabrication de moule
EP2110814A1 (fr)	2008-04-18	2009-10-21	Fujifilm Corporation	Procédé de fabrication d'une matrice et procédé de fabrication d'un support d'enregistrement d'informations optiques utilisant ensuite une matrice
WO2009130846A1 (fr)	2008-04-22	2009-10-29	富士フイルム株式会社	Procédé d’exposition au laser, procédé de façonnage d’une couche de résine photosensible et procédé de fabrication d’un modèle de moulage
WO2009136624A1 (fr)	2008-05-09	2009-11-12	富士フイルム株式会社	Composition d'absorption d'ultraviolets
WO2010023789A1 (fr)	2008-08-29	2010-03-04	富士フイルム株式会社	Elément de formation de motifs et procédé de fabrication associé
WO2010023790A1 (fr)	2008-08-29	2010-03-04	富士フイルム株式会社	Procédé de fabrication d'un corps de formation de motifs et appareil de traitement de faisceau électromagnétique
WO2010035483A1 (fr)	2008-09-25	2010-04-01	富士フイルム株式会社	Support d’enregistrement d’informations optique, procédé d’enregistrement d’informations, et colorant complexe métallique azoïque
WO2010041470A1 (fr)	2008-10-10	2010-04-15	富士フイルム株式会社	Support d'enregistrement d'informations optique, procédé d'enregistrement d'informations et photosensibilisateur
EP2216680A2 (fr)	2009-02-04	2010-08-11	FUJIFILM Corporation	Particules fines et leur procédé de production
EP2219053A1 (fr)	2009-02-04	2010-08-18	FUJIFILM Corporation	Film réfléchissant les rayons calorifiques, structure réfléchissant les rayons calorifiques et procédé de fabrication correspondant
WO2010093062A1 (fr)	2009-02-13	2010-08-19	Fujifilm Corporation	Dispositif d'électroluminescence organique, et son procédé de production

1983
- 1983-08-23 JP JP58153393A patent/JPS6044390A/ja active Granted

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0597826A3 (fr) *	1987-08-05	1995-08-30	Canon Kk	Support d'enregistrement de données.
JPS6440389A (en) *	1987-08-06	1989-02-10	Taiyo Yuden Kk	Optical data recording medium
US5330542A (en) *	1990-05-25	1994-07-19	Mitsubishi Kasei Corporation	Dye-incorporated composition
WO2003042989A1 (fr) *	2001-11-13	2003-05-22	Ciba Specialty Chemicals Holding Inc.	Compositions comprenant au moins un colorant a base d'oxonol et au moins un complexe metallique
WO2004102551A3 (fr) *	2003-05-14	2005-03-31	Ciba Sc Holding Ag	Nouveaux metaux complexes
WO2007119672A1 (fr)	2006-04-10	2007-10-25	Fujifilm Corporation	Support d'enregistrement optique, procédé d'enregistrement d'informations visibles et utilisation d'un colorant
WO2008108406A1 (fr)	2007-03-05	2008-09-12	Fujifilm Corporation	Composé pour résine photosensible, solution de résine photosensible, et procédé de gravure utilisant la solution de résine photosensible
WO2008123010A1 (fr)	2007-03-05	2008-10-16	Fujifilm Corporation	Elément électroluminescent, procédé de fabrication de l'élément électroluminescent, élément optique et procédé de fabrication de l'élément optique
EP1998329A2 (fr)	2007-06-01	2008-12-03	Fujifilm Corporation	Support d'enregistrement d'informations optiques et procédé d'enregistrement d'informations
WO2009022442A1 (fr)	2007-08-16	2009-02-19	Fujifilm Corporation	Procédé pour fabriquer un support sur lequel des informations sont enregistrées par un motif de cuvette
WO2009050858A1 (fr)	2007-10-15	2009-04-23	Fujifilm Corporation	Procédé de nettoyage d'une couche de support d'enregistrement de type en mode thermique, procédé de fabrication d'un produit comportant des creux et des saillies, procédé de fabrication d'un élément électroluminescent et procédé de fabrication d'un élément optique
WO2009110046A1 (fr)	2008-03-05	2009-09-11	富士フイルム株式会社	Procédé de traitement d'une pièce de travail ayant une couche photosensible
WO2009113272A1 (fr)	2008-03-10	2009-09-17	富士フイルム株式会社	Procédé de traitement de moule et procédé de fabrication de moule
EP2110814A1 (fr)	2008-04-18	2009-10-21	Fujifilm Corporation	Procédé de fabrication d'une matrice et procédé de fabrication d'un support d'enregistrement d'informations optiques utilisant ensuite une matrice
WO2009130846A1 (fr)	2008-04-22	2009-10-29	富士フイルム株式会社	Procédé d’exposition au laser, procédé de façonnage d’une couche de résine photosensible et procédé de fabrication d’un modèle de moulage
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Also Published As

Publication number	Publication date
JPH0475146B2 (fr)	1992-11-30

Publication	Publication Date	Title
JPS6044390A (ja)	1985-03-09	光記録媒体
JPS6019587A (ja)	1985-01-31	光記録媒体
JPS5967092A (ja)	1984-04-16	光記録媒体
WO1985004372A1 (fr)	1985-10-10	Support d'enregistrement optique
JPS5981194A (ja)	1984-05-10	光記録媒体
JPS6036190A (ja)	1985-02-25	光記録媒体
JPS6044555A (ja)	1985-03-09	光記録媒体
JPH0441067B2 (fr)	1992-07-07
JPS6018387A (ja)	1985-01-30	光記録媒体
JPS6044554A (ja)	1985-03-09	光記録媒体
JPH0472712B2 (fr)	1992-11-18
JPS6019586A (ja)	1985-01-31	光記録媒体
JPS6035054A (ja)	1985-02-22	光記録媒体
JPS5955794A (ja)	1984-03-30	光記録媒体
JPS5971895A (ja)	1984-04-23	光記録媒体
JPS59190895A (ja)	1984-10-29	光記録媒体
JPS59192595A (ja)	1984-10-31	光記録媒体
JPS60205841A (ja)	1985-10-17	光記録媒体
JPS60204396A (ja)	1985-10-15	光記録媒体
JPS59124891A (ja)	1984-07-19	光記録媒体
JPS59201243A (ja)	1984-11-14	光記録媒体
JPS59124897A (ja)	1984-07-19	光記録媒体
JPS6092893A (ja)	1985-05-24	光記録媒体
JPS60204395A (ja)	1985-10-15	光記録媒体
JPS59188855A (ja)	1984-10-26	光記録媒体

JPS6044390A - 光記録媒体 - Google Patents

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ID=15561505

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Cited By (23)

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