CN1462435A - 在信息层中包含酞菁染料作为吸光化合物的光数据载体 - Google Patents
在信息层中包含酞菁染料作为吸光化合物的光数据载体 Download PDFInfo
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- CN1462435A CN1462435A CN01816131.6A CN01816131A CN1462435A CN 1462435 A CN1462435 A CN 1462435A CN 01816131 A CN01816131 A CN 01816131A CN 1462435 A CN1462435 A CN 1462435A
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- 230000003287 optical effect Effects 0.000 title claims abstract description 26
- 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 title claims abstract description 21
- 150000001875 compounds Chemical class 0.000 title claims abstract description 15
- 238000004040 coloring Methods 0.000 title abstract 2
- 239000000758 substrate Substances 0.000 claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- -1 heterocyclic amine Chemical class 0.000 claims description 64
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 230000014509 gene expression Effects 0.000 claims description 18
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 229910052736 halogen Inorganic materials 0.000 claims description 17
- 150000002367 halogens Chemical class 0.000 claims description 17
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 125000004429 atom Chemical group 0.000 claims description 16
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 11
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 9
- 238000001704 evaporation Methods 0.000 claims description 9
- 230000008020 evaporation Effects 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 239000001007 phthalocyanine dye Substances 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 125000003368 amide group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 230000001681 protective effect Effects 0.000 claims description 6
- 238000004528 spin coating Methods 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 229910052748 manganese Inorganic materials 0.000 claims description 5
- 239000011572 manganese Substances 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 239000003446 ligand Substances 0.000 claims description 4
- 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 claims description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- 125000004647 alkyl sulfenyl group Chemical group 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims description 2
- 229910052790 beryllium Inorganic materials 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229910052733 gallium Inorganic materials 0.000 claims description 2
- 229910052732 germanium Inorganic materials 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- 229910052745 lead Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 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 claims description 2
- 229910052753 mercury Inorganic materials 0.000 claims description 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 150000003053 piperidines Chemical class 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 125000005031 thiocyano group Chemical group S(C#N)* 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 10
- 229910052731 fluorine Inorganic materials 0.000 description 8
- 229910052794 bromium Inorganic materials 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 125000003282 alkyl amino group Chemical group 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 238000002310 reflectometry Methods 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 239000011358 absorbing material Substances 0.000 description 3
- 125000004915 dibutylamino group Chemical group C(CCC)N(CCCC)* 0.000 description 3
- 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 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ZOAMZFNAPHWBEN-UHFFFAOYSA-N 2-$l^{1}-oxidanylpropane Chemical compound CC(C)[O] ZOAMZFNAPHWBEN-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000013500 data storage Methods 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- HLYVNXRHROOICH-UHFFFAOYSA-N o-propan-2-ylhydroxylamine Chemical compound CC(C)ON HLYVNXRHROOICH-UHFFFAOYSA-N 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 125000004894 pentylamino group Chemical group C(CCCC)N* 0.000 description 2
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 description 1
- ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 1,2-dihydrophenazine Chemical compound C1=CC=C2N=C(C=CCC3)C3=NC2=C1 ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 0.000 description 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 241000931526 Acer campestre Species 0.000 description 1
- 239000004923 Acrylic lacquer Substances 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical class N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- 230000004447 accommodation reflex Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 201000009310 astigmatism Diseases 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004802 cyanophenyl group Chemical group 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- CYEDOLFRAIXARV-UHFFFAOYSA-N ethyl propyl carbonate Chemical compound CCCOC(=O)OCC CYEDOLFRAIXARV-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 125000002541 furyl group Chemical group 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
- 239000010931 gold Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- RWGFKTVRMDUZSP-UHFFFAOYSA-N isopropyl-benzene Natural products CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- YTZKOQUCBOVLHL-UHFFFAOYSA-N p-methylisopropylbenzene Natural products CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 1
- 229920006391 phthalonitrile polymer Polymers 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000012749 thinning agent Substances 0.000 description 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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Abstract
本发明涉及一种光数据载体,其包括优选透明的、如果需要已经被一层或多层反射层涂覆的基底。在所述基底的表面上涂有用光可记录的信息层,和如果需要一层或多层反射层和如果需要保护层或者另一基底或者覆盖层。所述光学数据载体可以用蓝光,优选激光记录和读取。所述的信息层包括吸收光的化合物和如果需要粘结剂。本发明的光学数据载体的特征在于使用至少一种酞菁染料作为吸收光的化合物。
Description
技术背景
本发明涉及一次性可记录光数据载体,该载体在信息层中包括至少一种酞菁染料作为吸收光的化合物。
一次性可记录光数据载体在使用特定的光吸收物质或其混合物下特别适合于在高密度可记录光数据存储器中使用,该存储器通过蓝激光二极管,特别是GaN或SHG激光二极管(360至460纳米)工作,和/或适合于在DVD-R和CD-R盘中使用,该盘通过红(635纳米至660纳米)和红外线(780至830纳米)激光二极管工作,以及上述染料通过旋涂、蒸镀或溅射涂覆在聚合物基底上,特别是聚碳酸酯上。
近来,该一次性可记录压缩光盘(CD-R,780纳米)的数量急剧增长,并且其是技术上成形的体系。
不久前,在市场上出现了最新一代的光数据存储器-DVD。通过使用短波激光照射(635至660纳米)和较高数值孔径NA可以提高该存储器的密度。在这种情况下,该一次性可记录格式是DVD-R。
现在,已经开发出利用具有高激光功率的蓝激光二极管(基础GaN,JP-A-08 191 171或者
Second Harmonic
Generation SHG JP-A-09050 629)(360至460纳米)的光数据存储器格式。因此,在这一代中同样也可以使用可记录光数据存储器。可获得的存储器密度取决于在信息平面中激光点的聚焦。这里,该点的大小通过激光波长λ/NA来衡量。NA是所使用物镜透镜的数值孔径。为了获得尽可能高的存储器密度,力求使用尽可能小的波长λ。现在,在半导体激光二极管的基础上,390纳米是可能的。
在专利文献中描述了基于染料的同样适合于CD-R和DVD-R体系的可记录光数据存储器(JP-A11 043 481和JP-A10 181 206)。这里,对于高的反射性和高的读取信号的调制高度以及在记录事件时足够的敏感性使用位于染料的吸收峰值的长波缘的下部的CD-R的IR波长780纳米,位于染料的吸收峰值的短波缘的下部的DVD-R的红色波长635纳米或650纳米(参见EP-A519 395和WO-A00/09522)。在JP-A02 557 335、JP-A10 058 828、JP-A06 336 086、JP-A02865 955、WO-A09 917 284和US-A5 266 699中这种概念被延伸至在吸收峰值的短波缘上450纳米的工作波长和长波缘上红色和IR的范围。
除上述光性能外,由吸收光的有机基底形成的可记录信息层具有尽可能无定形的形态,以便在记录或读取时保持尽可能小的噪声信号。对此特别优选地是,在真空中,在随后用金属或介电层覆盖时,在通过旋涂涂覆由溶液形成的物质、通过溅射或通过蒸镀和/或升华涂覆物质时防止吸收光物质的结晶。
由吸收光的物质形成的无定形层优选应该具有高的热稳定性,因为否则由有机或无机材料形成的其它层(通过溅射或蒸镀涂覆在该吸收光的信息层上)通过扩散形成模糊的界面,并因此对反射性产生不利的影响。此外,界面上的具有太低热稳定性的吸收光的物质扩散到其中的聚合物载体中并再次对反射性产生不利影响。
在上述溅射或蒸镀时,在高真空中,具有过高蒸汽压的吸收光的物质可以升华成另外的层,并因此降低所需的涂层厚度。这再次导致对反射性的不利影响。
因此本发明的任务是提供适合的化合物,其满足在360至460纳米的激光波长范围中,在特别是用于高密度可记录光数据存储器格式的一次性可记录光数据载体中的信息层中使用时的高要求(如光稳定性、有利的信噪比、在基底材料上无害的涂层等)。
令人惊奇地发现,选自酞菁类的吸收光的化合物可以特别好地满足上述各种要求。酞菁在对激光来说重要的波长范围360至460纳米中(所谓的B-或Soret-波段)具有强的吸收性。
因此,本发明涉及光数据载体,其包括优选透明的、如果需要已经被一层或多层反射层涂覆的基底,在其表面上涂有用光可记录的信息层,如果需要一层或多层反射层和如果需要保护层或者另外的基底或者覆盖层,其可以用蓝光,优选激光,特别优选360至460纳米的光,更优选380至420纳米的光,最优选390至410纳米的光记录和读取,其中所述的信息层包括吸收光的化合物和如果需要粘结剂,其特征在于,使用至少一种酞菁作为吸收光的化合物。
在优选的实施方案中,使用式(I)化合物作为酞菁
MPc[R3]w[R4]x[R5]y[R6]z (I)
其中
Pc 表示酞菁,其中
M 表示二个独立的H-原子、代表二价金属原子或代表式
或者表示式(Ic)的三价单一轴向取代的和单一轴向
配位的金属原子
其中在带电荷的配位体X2或X1的情况下,通过平衡离
子例如阴离子An或阳离子Kat补偿电荷,
基团R3至R6相应于酞菁环的取代基,其中
X1和X2 相互独立地表示卤素,如F、Cl、Br、I;羟基;氧;
氰基;氰硫基;氰氧基;链烯基;炔基;芳基硫基;
二烷基氨基;烷基;烷氧基;酰氧基;烷基硫基;芳
基;芳氧基;-O-SO2R8;-O-PR10R11;-O-P(O)R12R13;
-O-SiR14R15R16;NH2;烷基氨基和杂环胺的基团,
R3、R4、R5和R6相互独立地表示卤素,如F、Cl、Br、I;氰基;硝基;
烷基;芳基;烷基氨基;二烷基氨基;烷氧基;烷基
硫基;芳基氧基;芳基硫基;SO3H、SO2NR1R2;CO2R9;
CONR1R2;NH-COR7或式-(B)m-D的基团,其中
B 表示选自直接键、CH2、CO、CH(烷基)、C(烷基)2、
NH、S、O或-CH=CH-的桥单元(Brückenglied),其
中(B)m表示桥单元B的化学上有意义的序列,m=1至
10,优选m=1、2、3或4,
或者表示金属茂基团或者金属茂羰基,其中金属中心
是钛、锰、铁、钌或者锇,
Z1和Z2 相互独立地表示NR′R″、OR″或SR″,
Y1 表示NR′、O或S,Y2表示NR′,
n 表示1至10,和
R′和R″ 相互独立地表示氢、烷基、环烷基、芳基或杂芳基,
链的碳原子之一上的直接键或者桥,
w、x、y和z 相互独立地表示0至4,并且w+x+y+z≤16
R1和R2 相互独立地表示氢、烷基、羟基烷基、芳基或R1和R2
与它们连接的氮原子一起形成杂环的5-、6-或7-元
环,如果需要在其它杂原子的参与下,特别是选自O、
N和S的杂原子,其中NR1R2特别地表示吡咯烷基、哌
啶子基或吗啉代,
R7至R16 相互独立地表示烷基、芳基、杂芳基或氢,特别地表
示烷基、芳基或杂芳基,
An- 表示阴离子,特别地表示卤阴离子、C1-至C20-烷基
COO-、甲酸根、草酸根、乳酸根、甘醇酸根、柠檬酸根、
CH3OSO3 -、NH2SO3 -、CH3SO3 -、1/2SO4 2-或1/3PO4 3-。
在M表示式(Ic)基团,特别是具有Co(III)作为金属原子的情况下,作为在X1和X2的意义中的杂环胺配位体或取代基优选吗啉、哌啶、哌嗪、吡啶、2,2-联吡啶、4,4-联吡啶、哒嗪、嘧啶、吡嗪、咪唑、苯并咪唑、异噁唑、苯并异噁唑、噁唑、苯并噁唑、噻唑、苯并噻唑、喹啉、吡咯、吲哚、3,3-二甲基吲哚,它们在每种情况下在氮原子上被金属原子配位或取代。
烷基-、烷氧基-、芳基-和杂环基团如果需要可以携带其它的基团,例如烷基、卤素、羟基、羟基烷基、氨基、烷基氨基、二烷基氨基、硝基、氰基、CO-NH2、烷氧基、烷氧基羰基、吗啉代、哌啶子基、吡咯烷基、吡咯烷酮基、三烷基甲硅烷基、三烷基甲硅烷氧基或苯基。烷基和烷氧基基团可以是饱和的、不饱和的、直链或支链的,烷基可以部分或全卤化,烷基和烷氧基基团可以被乙氧基化或丙氧基化或甲硅烷基化。在芳基或杂环基上相邻的烷基和/或烷氧基基团可以一起构成三元或四元桥。
优选(I)化合物,其中对于基团R1至R16、R′、R″和对于配位体或取代基X1和X2下列内容是合适的:
名称为“烷基”的取代基优选表示C1-C16-烷基,特别是C1-C6-烷基,其如果需要被卤素,如氯、溴、氟,羟基,氰基和/或C1-C6-烷氧基取代。
名称为“烷氧基”的取代基优选表示C1-C16-烷氧基,特别是C1-C6-烷氧基,其如果需要被卤素,如氯、溴、氟,羟基,氰基和/或C1-C6-烷基取代。
名称为“环烷基”的取代基优选表示C4-C8-环烷基,特别是C5-C6-环烷基,其如果需要被卤素,如氯、溴或氟,羟基,氰基和/或C1-C6-烷基取代。
名称为“链烯基”的取代基优选表示C6-C8-链烯基,其如果需要被卤素,如氯、溴或氟,羟基,氰基和/或C1-C6-烷基取代,特别地链烯基表示烯丙基。
含义为“杂芳基”的取代基优选表示具有5-至7-元环的杂环基,其优选包括选自氮、硫和/或氧的杂原子,并且如果需要与芳族环稠合或者如果需要携带其它的取代基,例如卤素、羟基、氰基和/或烷基,其中特别优选的是:吡啶基、呋喃基、噻吩基、噁唑基、噻唑基、咪唑基、喹啉基、苯并噁唑基、苯并噻唑基和苯并咪唑基,
名称为“芳基”的取代基优选表示C6-C10-芳基,特别是苯基和萘基,其如果需要被卤素,如F、Cl,羟基,C1-C6-烷基,C1-C6-烷氧基,NO2和/或CN取代。
R3、R4、R5和R6相互独立地优选表示氯、氟、溴、碘、氰基、甲基、乙基、丙基、异丙基、丁基、异丁基、叔丁基、戊基、叔戊基、羟基乙基、3-二甲基氨基丙基、3-二乙基氨基丙基、苯基、对-叔丁基苯基、对-甲氧基苯基、异丙基苯基、三氟甲基苯基、萘基、甲基氨基、乙基氨基、丙基氨基、异丙基氨基、丁基氨基、异丁基氨基、叔丁基氨基、戊基氨基、叔戊基氨基、苄基氨基、甲基苯基己基氨基、羟基乙基氨基、氨基丙基氨基、氨基乙基氨基、3-二甲基氨基丙基氨基、3-二乙基氨基丙基氨基、二乙基氨基乙基氨基、二丁基氨基丙基氨基、吗啉基丙基氨基、哌啶基(piperidino)丙基氨基、吡咯烷基丙基氨基、吡咯烷基丙基氨基、3-(甲基-羟基乙基氨基)丙基氨基、甲氧基乙基氨基、乙氧基乙基氨基、甲氧基丙基氨基、乙氧基丙基氨基、甲氧基乙氧基丙基氨基、3-(2-乙基己基氧基)丙基氨基、异丙基氧基丙基氨基、二甲基氨基、二乙基氨基、二乙醇氨基、二丙基氨基、二异丙基氨基、二丁基氨基、二异丁基氨基、二-叔丁基氨基、二戊基氨基、二-叔戊基氨基、双(2-乙基己基)氨基、双(氨基丙基)氨基、双(氨基乙基)氨基、双(3-二甲基氨基丙基)氨基、双(3-二乙基氨基丙基)氨基、双(二乙基氨基乙基)氨基、双(二丁基氨基丙基)氨基、二(吗啉基丙基)氨基、二(哌啶基丙基)氨基、二(吡咯烷基丙基)氨基、二(吡咯烷酮基丙基)氨基、双(3-(甲基-羟基乙基氨基)丙基)氨基、二甲氧基乙基氨基、二乙氧基乙基氨基、二甲氧基丙基氨基、二乙氧基丙基氨基、二(甲氧基乙氧基乙基)氨基、二(甲氧基乙氧基丙基)氨基、双(3-(2-乙基己基氧基)丙基)氨基、二(异丙基氧基异丙基)氨基、甲氧基、乙氧基、丙氧基、异丙氧基、丁氧基、异丁氧基、叔丁氧基、戊氧基、叔戊氧基、甲氧基乙氧基、乙氧基乙氧基、甲氧基丙基氧基、乙氧基丙基氧基、甲氧基乙氧基丙基氧基、3-(2-乙基-己基氧基)丙基氧基、甲基硫基、乙基硫基、丙基硫基、异丙基硫基、丁基硫基、异丁基硫基、叔丁基硫基、戊基硫基、叔戊基硫基、苯基、甲氧基苯基、三氟甲基苯基、萘基、CO2R7、CONR1R2、NHCOR7、SO3H、SO2NR1R2或者代表下式的基团或
其中(B)m表示 或
这里星号(*)表示与5-环的链接。
M1 表示Mn或Fe阳离子,
w、x、y和z相互独立地表示0至4和W+x+y+z≤12,
NR1R2表示氨基、甲基氨基、乙基氨基、丙基氨基、异丙基氨基、丁基氨基、异丁基氨基、叔丁基氨基、戊基氨基、叔戊基氨基、苄基氨基、甲基苯基己基氨基、2-乙基-1-己基氨基、羟基乙基氨基、氨基丙基氨基、氨基乙基氨基、3-二甲基氨基丙基氨基、3-二乙基氨基丙基氨基、吗啉基丙基氨基、哌啶基(Piperidino)丙基氨基、吡咯烷基丙基氨基、吡咯烷酮丙基氨基、3-(甲基羟基乙基氨基)丙基氨基、甲氧基乙基氨基、乙氧基乙基氨基、甲氧基丙基氨基、乙氧基丙基氨基、甲氧基乙氧基丙基氨基、3-(2-乙基己基氧基)丙基氨基、异丙基氧基异丙基氨基、二甲基氨基、二乙基氨基、二丙基氨基、二异丙基氨基、二丁基氨基、二异丁基氨基、二-叔丁基氨基、二戊基氨基、二-叔戊基氨基、双(2-乙基己基)氨基、二羟基乙基氨基、双(氨基丙基)氨基、双(氨基乙基)氨基、双(3-二甲基氨基丙基)氨基、双(3-二乙基氨基丙基)氨基、二(吗啉基丙基)氨基、二(哌啶基(Piperidino)丙基)氨基、二(吡咯烷基丙基)氨基、二(吡咯烷酮基丙基)氨基、双(3-(甲基-羟基乙基氨基)丙基)氨基、二甲氧基乙基氨基、二乙氧基乙基氨基、二甲氧基丙基氨基、二乙氧基丙基氨基、二(甲氧基乙氧基丙基)氨基、双(3-(2-乙基己基氧基)丙基)氨基、二(异丙基氧基异丙基)氨基、苯胺基、对-甲苯氨基、对-叔丁基苯胺基、对-茴香氨基、异丙基苯胺基或萘基氨基,或者NR1R2表示吡咯烷基、哌啶基(Piperidino)、哌嗪基或吗啉代,
R7和R16相互独立地表示氢、甲基、乙基、丙基、异丙基、丁基、异丁基、叔丁基、戊基、叔戊基、苯基、对-叔丁基苯基、对-甲氧基苯基、异丙基苯基、对-三氟甲基苯基、氰基苯基、萘基、4-吡啶基、2-吡啶基、2-喹啉基、2-吡咯基或2-吲哚基,
其中
烷基、烷氧基、芳基和杂环基如果需要可以携带其它基团,例如烷基、卤素、羟基、羟基烷基、氨基、烷基氨基、二烷基氨基、硝基、氰基、CO-NH2、烷氧基、烷氧基羰基、吗啉代、哌啶基(Piperidino)、吡咯烷基、吡咯烷酮基、三烷基甲硅烷基、三烷基硅氧烷基或苯基,烷基和/或烷氧基可以是饱和的、不饱和的、直链或支链的,烷基可以是部分或全卤化的,烷基和/或烷氧基可以被乙氧基化或丙氧基化或甲硅烷化,在芳基或杂环基上相邻的烷基和/或烷氧基一起构成三或四元桥。
在本申请的范围中,还原氧化聚合系特别地被理解为在Angew.Chem.1978,第927页和在Topics of Current Chemistry,92卷,第1页(1980)中描述的还原氧化聚合系。
优选是对-亚苯基二胺、吩噻嗪、二氢吩嗪、联吡啶鎓盐(Viologene)、喹啉并二甲烷(Chinodimethane)。
在优选的实施方案中,使用式(I)的酞菁,
其中
M 表示二个独立的H原子或表示选自Cu、Ni、Zn、Pd、Pt、Fe、Mn、Mg、Co、Ru、Ti、Be、Ca、Ba、Cd、Hg、Pb或Sn的二价金属原子Me,或者
M 表示式(Ia)的三价的单一(einfach)轴向取代的金属原子,其中金属Me选自Al、Ga、Ti、In、Fe和Mn,或者
M 表示式(Ib)的四价的二次轴向取代的金属原子,其中金属Me选自Si、Ge、Sn、Zr、Cr、Ti、Co和V。
特别优选地,X1和X2是卤素,特别是氯;芳基氧基,特别是苯氧基;或者烷氧基,特别是甲氧基。
R3至R6特别地表示卤素、C1-C6-烷基或C1-C8-烷氧基。
最优选式I的酞菁,其中M表示式(Ia)和式(Ib)的基团,和w、x、y和z在每种情况下表示0,和X1和/或X2在每种情况下表示卤素。
本发明使用的酞菁可以按照已知的方法制备,例如:
-在相应金属、金属卤化物或金属氧化物存在下,通过由相应取代的邻苯二甲腈(Phthalodinitrilen)的核合成(Kernsynthese),
-通过酞菁的化学变化,例如通过酞菁的氯磺化或氯化和其它的反应,例如由此形成的产物的缩合或取代。
-轴向取代基X1和X2通常由相应卤化物通过交换来制备。
该吸收光的化合物优选应该是可热变化的。热变化优选在<600℃下进行。这种变化例如可以是吸收光的化合物的发色中心的分解或化学变化。
该可记录吸光物质保证该光数据载体在未写状态下的足够高的反射性以及足够高的用于在采用聚焦的兰光,特别是激光(优选具有360至460纳米的波长)逐点照射时信息层热降解的吸收。在数据载体上写和未写位置之间的对比是通过在热降解之后改变的信息层的光学性能导致的射入光的振幅和相的反射性的变化来实现的。
也就是说,优选该光数据载体可以通过波长为360至460纳米的激光来记录和读取。
涂覆酞菁优选通过旋涂、溅射或真空蒸镀(Vakuumbedampfung)进行。特别地在有机介质或含水介质中不溶解的酞菁,优选其中w、x、y和z在每种情况下表示0和M表示或
这里X1和X2具有上述含义的式(I)的酞菁可以通过真空蒸镀或溅射。
对于通过旋涂涂覆,特别地考虑在有机介质或含水介质中溶解的酞菁。该酞菁可以相互混合或者与另外的具有类似光谱性能的染料混合。该信息层除酞菁外还可以包括添加剂,例如粘结剂、润湿剂、稳定剂、稀释剂和敏化剂以及其它组分。
该光数据存储器除信息层外还带有其它层,例如金属层、介电层以及保护层。金属和介电层特别可用于调节反射性和热平衡。金属根据激光波长可以是金、银、铝、合金等。介电层例如是二氧化硅和氮化硅。保护层例如是可光硬化的漆、粘结层和保护箔。
另外,该光数据载体的结构可以:
·包括优选透明的基底,在其表面上涂覆至少一层用光可记录的信息层、如果需要反射层和如果需要粘结层和另一优选透明的基底。
·包括优选透明的基底,在其表面上如果需要涂覆反射层、至少用光可记录的信息层、如果需要粘结层和透明的覆盖层。
此外,本发明涉及用蓝光,特别是激光,特别优选是波长为360至460纳米的激光可记录的本发明的光数据载体。
下面的实施例进一步详细说明本发明的内容。
实施例
在高真空(压力p≈2.10-5毫巴)下,将染料一氯-铝-酞菁(AlClPc)从电阻加热(resistiv geheizten)的钼舟上以约5/s的速度蒸镀在预制有凹槽的聚碳酸酯基底上。该涂层的厚度是约70纳米。该预制的有凹槽的聚碳酸酯基底是借助于注塑作为盘生产的。该盘的直径是120毫米和其厚度是0.6毫米。在注塑工艺中压制的凹槽结构的道间距(Spurabstand)是约1微米,这里凹槽深度和凹槽半宽度是约150纳米和约260纳米。将100纳米的Ag蒸汽沉积在以染料层作为信息载体的盘上。随后,通过旋涂涂覆UV-固化丙烯酸漆(Acryllack),并借助于UV-灯固化。借助于在光层(由GaN-二极管激光(λ=405纳米)组成)上形成的动力记录测试结构以产生线性偏振化的激光,对偏振化敏感的束分离器(Strahlteiler)、λ/4-薄片(Plttchen)和可移动的悬挂上的具有数值孔径NA=0.65的聚光透镜(Aktuatorlinse)。将从该盘反射的光借助于上述对偏振化敏感的束分离器从光径输出耦合,并且通过象散性的透镜聚焦在四象限探测器上。在线性速度V=5.24m/s和记录功率Pw=13mW时,测量的信噪比C/N=25dB。这里记录功率作为脉冲序列施加,其中该盘交替采用上述记录功率Pw照射1μs长和采用读取功率Pr=0.44mW4μs长。该盘一直采用这种脉冲序列照射直至其已经围绕自身旋转一次。之后采用读取功率Pr=0.44mW读取出如此产生的标记并测量上述信噪比C/N。
类似于实施例1,在具有相同厚度和凹槽结构的盘上蒸镀45纳米厚的二氯-硅-酞菁染料层。采用相同的光结构和相同的记录策略(记录功率Pw=13mW,读取功率Pr=0.44mW)在V=4.19m/s的线性速度下测量信噪比C/N=46dB。
类似于实施例1和2的做法,下面实施例同样使用酞菁并显示可比的性能。
类似于实施例1,在具有相同厚度和凹槽结构的盘上各自蒸镀70纳米厚的苯氧基-铝-酞菁染料层。如实施例1,采用相同的光结构和相同的记录策略(记录功率Pw=13mW,读取功率Pr=0.44mW)在V=5.24m/s的线性速度下测量信噪比C/N=22dB。
类似于实施例1,在具有相同厚度和凹槽结构的盘上各自蒸镀70纳米厚的双苯氧基-硅-酞菁染料层。如实施例1,采用相同的光结构和相同的记录策略(记录功率Pw=13mW,读取功率Pr=0.44mW)在V=5.24m/s的线性速度下测量信噪比C/N=23dB。
实施例5
Claims (7)
1、一种光数据载体,其包括优选透明的、如果需要已经被一层或多层反射层涂覆的基底,在其表面上涂有用光可记录的信息层,如果需要一层或多层反射层和如果需要保护层或者另外的基底或者覆盖层,其可以用蓝光,优选激光记录和读取,其中所述的信息层包括吸收光的化合物和如果需要粘结剂,其特征在于,使用至少一种酞菁染料作为吸收光的化合物。
2、权利要求1的光数据载体,其特征在于,所述酞菁染料相应于式(I)
MPc[R3]w[R4]x[R5]y[R6]z (I)
其中
Pc 表示酞菁,
M 表示二个独立的H-原子、表示二价金属原子或表示式
或者表示式(Ib)的四价的二次轴向取代的金属原子
或者表示式(Ic)的三价的单一轴向取代的和单一轴
其中在带电荷的配位体或取代基X1或X2的情况下,通
过平衡离子补偿电荷,
基团R3至R6相应于酞菁的取代基,
X1和X2 相互独立地表示卤素;羟基;氧;氰基;氰硫基;氰
氧基;链烯基;炔基;芳基硫基;二烷基氨基;烷基;
烷氧基;酰氧基;烷基硫基;芳基;芳氧基;-O-SO2R8;
-O-PR10R11;-O-P(O)R12R13;-O-SiR14R15R16;NH2;烷基
氨基和杂环胺的基团,
R3、R4、R5和R6相互独立地表示卤素;氰基;硝基;烷基;芳基;烷
基氨基;二烷基氨基;烷氧基;烷基硫基;芳基氧基;
芳基硫基;SO3H、SO2NR1R2;CO2R9;CONR1R2;NH-COR7
或式-(B)m-D的基团,其中
B 表示选自直接键、CH2、CO、CH(烷基)、C(烷基)2、
NH、S、O或-CH=CH-的桥单元,其中(B)m表示桥单
元B的化学上有意义的序列,m=1至10,优选m=1、2、
3或4,
或者表示金属茂基团或者金属茂羰基,其中金属中心
是钛、锰、铁、钌或锇,
Z1和Z2 相互独立地表示NR′R″、OR″或SR″,
Y1 表示NR′、O或S,Y2表示NR′,
n表示1至10,和
R′和R″ 相互独立地表示氢、烷基、环烷基、芳基或杂芳基,
链的碳原子之一上的直接键或者桥,
w、x、y和z 相互独立地表示0至4,并且w+x+y+z≤16
R1和R2 相互独立地表示烷基、羟基烷基、芳基或R1和R2与它
们连接的氮原子一起形成杂环的5-、6-或7-元环,
如果需要在其它杂原子的参与下,特别是选自O、N
和S的杂原子,其中NR1R2特别地表示吡咯烷基、哌啶
子基或吗啉代,
R7至R16 相互独立地表示烷基、芳基、杂芳基或氢。
3、权利要求2的光数据载体,其特征在于,
M表示二个独立的H原子或表示选自Cu、Ni、Zn、Pd、Pt、Fe、Mn、Mg、Co、Ru、Ti、Be、Ca、Ba、Cd、Hg、Pb和Sn的二价金属原子,或者表示式(Ia)的三价单一轴向取代的金属原子,其中Me表示Al、Ga、Ti、In、Fe或Mn,或者表示式(Ib)的四价金属原子,其中Me表示Si、Ge、Sn、Zn、Cr、Ti、Co或V。
4、权利要求2的光数据载体,其特征在于,
M表示式(Ia)或式(Ib)的基团,其中Me表示Al或Si,
X1和X2表示卤素,特别是氯;芳基氧基,特别是苯氧基或者烷氧基,特别是甲氧基,和
w、x、y和z在每种情况下表示0。
5、制备权利要求1的光数据载体的方法,其特征在于,使用酞菁颜料,如果需要与适合的粘结剂和添加剂和如果需要适合的溶剂一起涂覆优选透明的、如果需要用反射层已经涂覆的基底,并且如果需要提供有反射层、另外的中间层和如果需要保护层或另外的基底或覆盖层。
6、权利要求5的光数据载体的制备方法,其特征在于,借助于旋涂、溅射或蒸镀以酞菁染料涂覆。
7、具有记录的信息层的光数据载体,其是这样获得的,即用蓝光,优选激光,特别是波长为360至460纳米的激光记录权利要求1的光数据载体。
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DE10115227A DE10115227A1 (de) | 2001-03-28 | 2001-03-28 | Optischer Datenträger enthaltend in der Informationsschicht eine lichtabsorbierende Verbindung mit mehreren chromophoren Zentren |
DE10124585.8 | 2001-05-21 | ||
DE10124585A DE10124585A1 (de) | 2000-09-21 | 2001-05-21 | Optische Datenspeicher enthaltend ein Co-Phthalocyanin-Komplex in der mit Licht beschreibbaren Informationsschicht |
DE2001140165 DE10140165A1 (de) | 2001-08-22 | 2001-08-22 | Optischer Datenträger enthaltend in der Informationsschicht einen Phthalocyaninfarbstoff als lichtabsorbierende Verbindung |
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EP (1) | EP1323160A1 (zh) |
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CN (1) | CN1462435A (zh) |
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EP1377977A1 (en) * | 2001-03-28 | 2004-01-07 | Bayer Chemicals AG | Optical recording medium |
AU2002257686A1 (en) * | 2001-03-28 | 2002-10-15 | Bayer Aktiengesellschaft | Optical data medium containing, in the information layer, a dye as a lightabsorbing compound and having a protective covering layer of predetermined thickness |
JP4076739B2 (ja) * | 2001-06-13 | 2008-04-16 | 富士フイルム株式会社 | 光記録媒体 |
TWI242206B (en) * | 2001-06-22 | 2005-10-21 | Fuji Photo Film Co Ltd | Optical information recording medium |
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US6896945B2 (en) * | 2001-08-22 | 2005-05-24 | Bayer Aktiengesellschaft | Optical data carrier comprising a phthalocyanine dye as light-absorbent compound in the information layer |
KR20050044487A (ko) * | 2001-11-15 | 2005-05-12 | 시바 스페셜티 케미칼스 홀딩 인크. | 금속 착물을 함유하는 기록 가능한 고용량 광학 저장 매체 |
EP1316950A1 (en) * | 2001-11-30 | 2003-06-04 | Fuji Photo Film Co., Ltd. | Optical information recording medium |
DE60326895D1 (de) * | 2002-01-23 | 2009-05-07 | Fujifilm Corp | Optisches Informationsaufzeichnungsmedium |
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JP4136834B2 (ja) * | 2003-07-16 | 2008-08-20 | 富士フイルム株式会社 | 光情報記録媒体 |
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JP4505206B2 (ja) * | 2003-10-17 | 2010-07-21 | 富士フイルム株式会社 | 光情報記録媒体および情報記録方法、並びに、色素化合物 |
JP2007522973A (ja) * | 2004-02-24 | 2007-08-16 | 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 | 青色レーザーを使用して書き込みが可能な光学記録材料 |
JP4327668B2 (ja) * | 2004-06-25 | 2009-09-09 | 太陽誘電株式会社 | 光情報記録媒体 |
TW200705436A (en) * | 2005-06-29 | 2007-02-01 | Fujifilm Corp | Optical information-recording medium and information-recording method |
DE602007010092D1 (de) * | 2006-01-13 | 2010-12-09 | Mitsubishi Kagaku Media Co Ltd | Optisches aufzeichnungsmedium |
JP2007237480A (ja) * | 2006-03-06 | 2007-09-20 | Fujifilm Corp | 光情報記録媒体および情報記録方法 |
US20070243489A1 (en) * | 2006-04-14 | 2007-10-18 | Fujifilm Corporation | Optical information-recording medium, method for recording information, and compound |
JP2008018590A (ja) * | 2006-07-12 | 2008-01-31 | Fujifilm Corp | 光情報記録媒体及びその製造方法 |
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