DE602004001135T2 - Materialien für optische aufzeichnung mit hoher speicherdichte - Google Patents
Materialien für optische aufzeichnung mit hoher speicherdichte Download PDFInfo
- Publication number
- DE602004001135T2 DE602004001135T2 DE602004001135T DE602004001135T DE602004001135T2 DE 602004001135 T2 DE602004001135 T2 DE 602004001135T2 DE 602004001135 T DE602004001135 T DE 602004001135T DE 602004001135 T DE602004001135 T DE 602004001135T DE 602004001135 T2 DE602004001135 T2 DE 602004001135T2
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- Prior art keywords
- substituted
- alkyl
- unsubstituted
- sub
- radicals
- Prior art date
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- 230000003287 optical effect Effects 0.000 title claims abstract description 34
- 238000003860 storage Methods 0.000 title abstract description 8
- 239000000463 material Substances 0.000 title description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 49
- 239000000758 substrate Substances 0.000 claims abstract description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 15
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 14
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 12
- 229910052802 copper Inorganic materials 0.000 claims abstract description 9
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 9
- 150000003624 transition metals Chemical class 0.000 claims abstract description 9
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 6
- 229910052763 palladium Inorganic materials 0.000 claims abstract description 6
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 5
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 3
- 229910052711 selenium Inorganic materials 0.000 claims abstract description 3
- -1 nitro, cyano, thiocyanato, hydroxy Chemical group 0.000 claims description 91
- 125000000217 alkyl group Chemical group 0.000 claims description 36
- 150000003254 radicals Chemical class 0.000 claims description 28
- 125000003118 aryl group Chemical group 0.000 claims description 24
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 15
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 15
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 12
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 10
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 8
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 8
- 125000004414 alkyl thio group Chemical group 0.000 claims description 7
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 7
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 6
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 2
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004450 alkenylene group Chemical group 0.000 claims description 2
- 125000005724 cycloalkenylene group Chemical group 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 229950000688 phenothiazine Drugs 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 description 18
- 239000007787 solid Substances 0.000 description 14
- 238000010521 absorption reaction Methods 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000000975 dye Substances 0.000 description 10
- 239000010949 copper Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 150000001768 cations Chemical class 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 229920000515 polycarbonate Polymers 0.000 description 7
- 239000004417 polycarbonate Substances 0.000 description 7
- 0 C*(C)C(C)(*)C(*)(*)[N+](C)/C=C(\C)/* Chemical compound C*(C)C(C)(*)C(*)(*)[N+](C)/C=C(\C)/* 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
- 239000003446 ligand Substances 0.000 description 6
- 150000001450 anions Chemical class 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 238000002310 reflectometry Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000002318 adhesion promoter Substances 0.000 description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000002524 organometallic group Chemical group 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- NBUKAOOFKZFCGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)F NBUKAOOFKZFCGD-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- BNDRWEVUODOUDW-UHFFFAOYSA-N 3-Hydroxy-3-methylbutan-2-one Chemical compound CC(=O)C(C)(C)O BNDRWEVUODOUDW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XUKCHCCIHMDMEP-HJWRWDBZSA-N C(C1)CN/C1=C\c1nc(cccc2)c2[s]1 Chemical compound C(C1)CN/C1=C\c1nc(cccc2)c2[s]1 XUKCHCCIHMDMEP-HJWRWDBZSA-N 0.000 description 2
- FRFAKVNEEKBKJS-JXMROGBWSA-N C(CS1)N/C1=C\c1nc(cccc2)c2[s]1 Chemical compound C(CS1)N/C1=C\c1nc(cccc2)c2[s]1 FRFAKVNEEKBKJS-JXMROGBWSA-N 0.000 description 2
- FMZBXJBYUCGMLX-UHFFFAOYSA-N C(CS1)N/C1=N\c1nc(cccc2)c2[s]1 Chemical compound C(CS1)N/C1=N\c1nc(cccc2)c2[s]1 FMZBXJBYUCGMLX-UHFFFAOYSA-N 0.000 description 2
- FDWWUXMHPKDNOT-UHFFFAOYSA-N C(N1)=CS/C1=N/c1nc2ccccc2[s]1 Chemical compound C(N1)=CS/C1=N/c1nc2ccccc2[s]1 FDWWUXMHPKDNOT-UHFFFAOYSA-N 0.000 description 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 description 2
- DMQGUFRMHMBZHY-UHFFFAOYSA-N CC(C)N(C(C)C)C(S1)=NN/C1=N\c1nc(cccc2)c2[s]1 Chemical compound CC(C)N(C(C)C)C(S1)=NN/C1=N\c1nc(cccc2)c2[s]1 DMQGUFRMHMBZHY-UHFFFAOYSA-N 0.000 description 2
- SSXOOXDNWABGTM-UHFFFAOYSA-N CC(N1)=CS/C1=N/c1nc(cccc2)c2[s]1 Chemical compound CC(N1)=CS/C1=N/c1nc(cccc2)c2[s]1 SSXOOXDNWABGTM-UHFFFAOYSA-N 0.000 description 2
- ATLVOWPSFAKDRK-UKTHLTGXSA-N CC1(C)c(cccc2)c2N=C1/C=C1/SCCN1 Chemical compound CC1(C)c(cccc2)c2N=C1/C=C1/SCCN1 ATLVOWPSFAKDRK-UKTHLTGXSA-N 0.000 description 2
- DAULINHFBWDBTE-UHFFFAOYSA-N CCN(c1ccccc1N1)/C1=N/c1nc2ccccc2[s]1 Chemical compound CCN(c1ccccc1N1)/C1=N/c1nc2ccccc2[s]1 DAULINHFBWDBTE-UHFFFAOYSA-N 0.000 description 2
- MWWFETBVSIFPQO-UHFFFAOYSA-N CCOC(C(N1)=CS/C1=N/c1nc2ccccc2[s]1)=O Chemical compound CCOC(C(N1)=CS/C1=N/c1nc2ccccc2[s]1)=O MWWFETBVSIFPQO-UHFFFAOYSA-N 0.000 description 2
- ZVVPCMLXPLAMKP-UHFFFAOYSA-N CN(c1c(N2)ncnc1)/C2=N/c1nc(ncnc2)c2[n]1C Chemical compound CN(c1c(N2)ncnc1)/C2=N/c1nc(ncnc2)c2[n]1C ZVVPCMLXPLAMKP-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- DTCJSKWNRCKWGO-QGOAFFKASA-N OCC[n]1c2ccccc2nc1/C=C1/N(CCO)c(cccc2)c2N1 Chemical compound OCC[n]1c2ccccc2nc1/C=C1/N(CCO)c(cccc2)c2N1 DTCJSKWNRCKWGO-QGOAFFKASA-N 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- PYYMWWWYFRGRAN-UHFFFAOYSA-N c1c[s]c(/N=C2/SC=CN2)n1 Chemical compound c1c[s]c(/N=C2/SC=CN2)n1 PYYMWWWYFRGRAN-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- BHIWKHZACMWKOJ-UHFFFAOYSA-N methyl isobutyrate Chemical compound COC(=O)C(C)C BHIWKHZACMWKOJ-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- GPNDARIEYHPYAY-UHFFFAOYSA-N palladium(ii) nitrate Chemical compound [Pd+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O GPNDARIEYHPYAY-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 150000004707 phenolate Chemical class 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 2
- 229940031826 phenolate Drugs 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- GZRZIVBGDNCIOR-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]-2-phenylethane-1,2-dithione;nickel Chemical compound [Ni].C1=CC(N(C)C)=CC=C1C(=S)C(=S)C1=CC=CC=C1.C1=CC(N(C)C)=CC=C1C(=S)C(=S)C1=CC=CC=C1 GZRZIVBGDNCIOR-UHFFFAOYSA-N 0.000 description 1
- JPZYXGPCHFZBHO-UHFFFAOYSA-N 1-aminopentadecane Chemical compound CCCCCCCCCCCCCCCN JPZYXGPCHFZBHO-UHFFFAOYSA-N 0.000 description 1
- SPXOTSHWBDUUMT-UHFFFAOYSA-N 138-42-1 Chemical compound OS(=O)(=O)C1=CC=C([N+]([O-])=O)C=C1 SPXOTSHWBDUUMT-UHFFFAOYSA-N 0.000 description 1
- JRBAVVHMQRKGLN-UHFFFAOYSA-N 16,16-dimethylheptadecan-1-amine Chemical compound CC(C)(C)CCCCCCCCCCCCCCCN JRBAVVHMQRKGLN-UHFFFAOYSA-N 0.000 description 1
- YPJUNDFVDDCYIH-UHFFFAOYSA-M 2,2,3,3,4,4,4-heptafluorobutanoate Chemical compound [O-]C(=O)C(F)(F)C(F)(F)C(F)(F)F YPJUNDFVDDCYIH-UHFFFAOYSA-M 0.000 description 1
- ZRXNLCFJIKBZCA-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-ylmethyl)-1,3-benzothiazole Chemical compound C1=CC=C2SC(CC=3SC4=CC=CC=C4N=3)=NC2=C1 ZRXNLCFJIKBZCA-UHFFFAOYSA-N 0.000 description 1
- HZCFBULZGPEMOB-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-ylmethyl)-1,3-benzoxazole Chemical compound C1=CC=C2OC(CC=3OC4=CC=CC=C4N=3)=NC2=C1 HZCFBULZGPEMOB-UHFFFAOYSA-N 0.000 description 1
- QMGVWSJNPMFIJO-UHFFFAOYSA-N 2-(1,3-thiazol-2-ylmethyl)-1,3-thiazole Chemical compound N=1C=CSC=1CC1=NC=CS1 QMGVWSJNPMFIJO-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- QSKPIOLLBIHNAC-UHFFFAOYSA-N 2-chloro-acetaldehyde Chemical compound ClCC=O QSKPIOLLBIHNAC-UHFFFAOYSA-N 0.000 description 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- RJWBTWIBUIGANW-UHFFFAOYSA-N 4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1 RJWBTWIBUIGANW-UHFFFAOYSA-N 0.000 description 1
- AAIUWVOMXTVLRG-UHFFFAOYSA-N 8,8-dimethylnonan-1-amine Chemical compound CC(C)(C)CCCCCCCN AAIUWVOMXTVLRG-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- JVTVDWGTJQROAX-LVWGJNHUSA-N CCCCNc(cccc1)c1SC(/N=C1\Sc(cccc2)c2N1CCCC)=[IH] Chemical compound CCCCNc(cccc1)c1SC(/N=C1\Sc(cccc2)c2N1CCCC)=[IH] JVTVDWGTJQROAX-LVWGJNHUSA-N 0.000 description 1
- OCCABYXMMBNJMN-QFVZEHFCSA-N CN/C=C\SC(/N=C1\SC=C(c2ccccc2)N1C)=[IH] Chemical compound CN/C=C\SC(/N=C1\SC=C(c2ccccc2)N1C)=[IH] OCCABYXMMBNJMN-QFVZEHFCSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
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- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/253—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
- G11B7/2533—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins
- G11B7/2535—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins polyesters, e.g. PET, PETG or PEN
-
- 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
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/257—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers having properties involved in recording or reproduction, e.g. optical interference layers or sensitising layers or dielectric layers, which are protecting the recording layers
- G11B7/2572—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers having properties involved in recording or reproduction, e.g. optical interference layers or sensitising layers or dielectric layers, which are protecting the recording layers consisting essentially of organic materials
- G11B7/2575—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers having properties involved in recording or reproduction, e.g. optical interference layers or sensitising layers or dielectric layers, which are protecting the recording layers consisting essentially of organic materials resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Plural Heterocyclic Compounds (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH3312003 | 2003-03-03 | ||
| CH3312003 | 2003-03-03 | ||
| PCT/EP2004/050185 WO2004079732A1 (en) | 2003-03-03 | 2004-02-23 | Optical recording materials having high storage density |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE602004001135D1 DE602004001135D1 (de) | 2006-07-20 |
| DE602004001135T2 true DE602004001135T2 (de) | 2007-04-12 |
Family
ID=32932301
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE602004001135T Expired - Fee Related DE602004001135T2 (de) | 2003-03-03 | 2004-02-23 | Materialien für optische aufzeichnung mit hoher speicherdichte |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20060159882A1 (https=) |
| EP (1) | EP1599878B1 (https=) |
| JP (1) | JP2006523553A (https=) |
| KR (1) | KR20050115265A (https=) |
| CN (1) | CN1757066A (https=) |
| AT (1) | ATE329351T1 (https=) |
| DE (1) | DE602004001135T2 (https=) |
| RU (1) | RU2005130516A (https=) |
| TW (1) | TW200428381A (https=) |
| WO (1) | WO2004079732A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002082438A2 (en) * | 2001-03-21 | 2002-10-17 | Ciba Specialty Chemicals Holding Inc. | Optical recording materials having high storage density |
| DE602004010451T2 (de) * | 2003-04-15 | 2008-11-20 | Ricoh Co., Ltd. | Einmal beschreibbarer, mehrmals lesbarer optischer Datenträger und Verfahren zum Beschreiben und Lesen des Datenträgers |
| EP1719126A1 (en) * | 2004-02-23 | 2006-11-08 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Optical recording materials having high storage density |
| JP2008509029A (ja) * | 2004-08-10 | 2008-03-27 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 高い記憶密度を有する光記録材料 |
| EP1710793A1 (de) * | 2005-04-05 | 2006-10-11 | Ciba SC Holding AG | Metallchelate und ihre Verwendung in optischen Aufzeichnungsmedien mit hoher Speicherkapazität |
| CA2786425C (en) * | 2010-01-19 | 2016-12-20 | Sumitomo Seika Chemicals Co., Ltd. | Composition for ultraviolet absorbent substance and ultraviolet absorbent substance comprising same |
| JP5400717B2 (ja) * | 2010-06-30 | 2014-01-29 | 住友精化株式会社 | 合成樹脂用安定化剤、該安定化剤を含有する合成樹脂組成物および樹脂部材 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1932894A1 (de) * | 1969-06-28 | 1971-01-28 | Basf Ag | Metallkomplexfarbstoffe |
| AU5561198A (en) * | 1996-12-20 | 1998-07-17 | Ciba Specialty Chemicals Holding Inc. | Complex polymethine dyes and their use |
| US6162520A (en) * | 1997-09-17 | 2000-12-19 | Mitsui Chemicals, Inc. | Optical recording medium and dipyrromethene metal chelate compound for use therein |
| US6376664B1 (en) * | 1999-03-17 | 2002-04-23 | The Ohio State University | Cyclic bis-benzimidazole ligands and metal complexes thereof |
| US6479123B2 (en) * | 2000-02-28 | 2002-11-12 | Mitsui Chemicals, Inc. | Dipyrromethene-metal chelate compound and optical recording medium using thereof |
| WO2002082438A2 (en) * | 2001-03-21 | 2002-10-17 | Ciba Specialty Chemicals Holding Inc. | Optical recording materials having high storage density |
| EP1719126A1 (en) * | 2004-02-23 | 2006-11-08 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Optical recording materials having high storage density |
-
2004
- 2004-02-23 RU RU2005130516/04A patent/RU2005130516A/ru not_active Application Discontinuation
- 2004-02-23 EP EP04713552A patent/EP1599878B1/en not_active Expired - Lifetime
- 2004-02-23 AT AT04713552T patent/ATE329351T1/de not_active IP Right Cessation
- 2004-02-23 WO PCT/EP2004/050185 patent/WO2004079732A1/en not_active Ceased
- 2004-02-23 CN CNA2004800055757A patent/CN1757066A/zh active Pending
- 2004-02-23 US US10/546,077 patent/US20060159882A1/en not_active Abandoned
- 2004-02-23 JP JP2006505428A patent/JP2006523553A/ja not_active Withdrawn
- 2004-02-23 KR KR1020057016423A patent/KR20050115265A/ko not_active Withdrawn
- 2004-02-23 DE DE602004001135T patent/DE602004001135T2/de not_active Expired - Fee Related
- 2004-03-02 TW TW093105419A patent/TW200428381A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1599878B1 (en) | 2006-06-07 |
| US20060159882A1 (en) | 2006-07-20 |
| WO2004079732A1 (en) | 2004-09-16 |
| HK1082980A1 (en) | 2006-06-23 |
| ATE329351T1 (de) | 2006-06-15 |
| KR20050115265A (ko) | 2005-12-07 |
| JP2006523553A (ja) | 2006-10-19 |
| EP1599878A1 (en) | 2005-11-30 |
| CN1757066A (zh) | 2006-04-05 |
| DE602004001135D1 (de) | 2006-07-20 |
| RU2005130516A (ru) | 2006-06-27 |
| TW200428381A (en) | 2004-12-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: CIBA HOLDING INC., BASEL, CH |
|
| 8339 | Ceased/non-payment of the annual fee |