TW556186B - Optical data stores containing a Co-phthalocyanine complex in the information layer recordable using light - Google Patents
Optical data stores containing a Co-phthalocyanine complex in the information layer recordable using light Download PDFInfo
- Publication number
- TW556186B TW556186B TW090123263A TW90123263A TW556186B TW 556186 B TW556186 B TW 556186B TW 090123263 A TW090123263 A TW 090123263A TW 90123263 A TW90123263 A TW 90123263A TW 556186 B TW556186 B TW 556186B
- Authority
- TW
- Taiwan
- Prior art keywords
- bis
- isonitrile
- amine
- amino
- alkyl
- Prior art date
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- 230000003287 optical effect Effects 0.000 title claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 32
- -1 ammonium amine Chemical class 0.000 claims description 169
- 150000001412 amines Chemical class 0.000 claims description 58
- 125000000217 alkyl group Chemical group 0.000 claims description 44
- 239000010410 layer Substances 0.000 claims description 36
- 239000007789 gas Substances 0.000 claims description 33
- 125000003545 alkoxy group Chemical group 0.000 claims description 30
- 150000002527 isonitriles Chemical class 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 22
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- 125000001424 substituent group Chemical group 0.000 claims description 15
- 230000002079 cooperative effect Effects 0.000 claims description 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 13
- 239000000758 substrate Substances 0.000 claims description 13
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 claims description 10
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 10
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 10
- 125000001072 heteroaryl group Chemical group 0.000 claims description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
- 229910052794 bromium Inorganic materials 0.000 claims description 9
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 claims description 9
- 229910052731 fluorine Inorganic materials 0.000 claims description 9
- 239000011737 fluorine Substances 0.000 claims description 9
- 125000000623 heterocyclic group Chemical group 0.000 claims description 9
- 239000003446 ligand Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 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 claims description 9
- 229940105325 3-dimethylaminopropylamine Drugs 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 8
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 claims description 8
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 8
- 239000011241 protective layer Substances 0.000 claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 7
- 125000005605 benzo group Chemical group 0.000 claims description 7
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 7
- 125000005842 heteroatom Chemical group 0.000 claims description 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 125000001624 naphthyl group Chemical group 0.000 claims description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000007983 Tris buffer Substances 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 6
- 239000000853 adhesive Substances 0.000 claims description 6
- 230000001070 adhesive effect Effects 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 6
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 6
- 229910017052 cobalt Inorganic materials 0.000 claims description 5
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 5
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 229940100684 pentylamine Drugs 0.000 claims description 5
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 claims description 5
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 claims description 4
- NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 claims description 4
- VPBWZBGZWHDNKL-UHFFFAOYSA-N 3-pyrrolidin-1-ylpropan-1-amine Chemical compound NCCCN1CCCC1 VPBWZBGZWHDNKL-UHFFFAOYSA-N 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 239000010941 cobalt Substances 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 claims description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- JAGYUOOMORBKRO-UHFFFAOYSA-N n-propan-2-yloxypropan-2-amine Chemical compound CC(C)NOC(C)C JAGYUOOMORBKRO-UHFFFAOYSA-N 0.000 claims description 4
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052763 palladium Inorganic materials 0.000 claims description 4
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 3
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 3
- GELMWIVBBPAMIO-UHFFFAOYSA-N 2-methylbutan-2-amine Chemical compound CCC(C)(C)N GELMWIVBBPAMIO-UHFFFAOYSA-N 0.000 claims description 3
- DVFGEIYOLIFSRX-UHFFFAOYSA-N 3-(2-ethylhexoxy)propan-1-amine Chemical compound CCCCC(CC)COCCCN DVFGEIYOLIFSRX-UHFFFAOYSA-N 0.000 claims description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 claims description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 3
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 claims description 3
- WGQKYBSKWIADBV-UHFFFAOYSA-N aminomethyl benzene Natural products NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims description 3
- 150000003927 aminopyridines Chemical class 0.000 claims description 3
- 229940043279 diisopropylamine Drugs 0.000 claims description 3
- 229910052737 gold Inorganic materials 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims description 3
- FRCFWPVMFJMNDP-UHFFFAOYSA-N n-propan-2-ylaniline Chemical compound CC(C)NC1=CC=CC=C1 FRCFWPVMFJMNDP-UHFFFAOYSA-N 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000011877 solvent mixture Substances 0.000 claims description 3
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 3
- LYASTVLDAJIXBL-UHFFFAOYSA-N 1,3-benzothiazole-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=NC2=C1 LYASTVLDAJIXBL-UHFFFAOYSA-N 0.000 claims description 2
- QWEWLLNSJDTOKH-UHFFFAOYSA-N 1,3-thiazole-2-carboxamide Chemical compound NC(=O)C1=NC=CS1 QWEWLLNSJDTOKH-UHFFFAOYSA-N 0.000 claims description 2
- DZHBWZZPLRJLPP-UHFFFAOYSA-N 1-isocyano-2-(2-methoxyethoxy)ethane Chemical compound COCCOCC[N+]#[C-] DZHBWZZPLRJLPP-UHFFFAOYSA-N 0.000 claims description 2
- QPFCLGADWIWYFW-UHFFFAOYSA-N 2,2-diethoxypropanenitrile Chemical compound CCOC(C)(C#N)OCC QPFCLGADWIWYFW-UHFFFAOYSA-N 0.000 claims description 2
- QDSMOWYMYIABBZ-UHFFFAOYSA-N 2,2-dimethoxypropanenitrile Chemical compound COC(C)(OC)C#N QDSMOWYMYIABBZ-UHFFFAOYSA-N 0.000 claims description 2
- WILCBFNNYBOTNE-UHFFFAOYSA-N 2-(2-methoxyethoxy)propanenitrile Chemical compound COCCOC(C)C#N WILCBFNNYBOTNE-UHFFFAOYSA-N 0.000 claims description 2
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 2
- WPYUCWSMVJJWFI-UHFFFAOYSA-N 2-ethoxyacetonitrile Chemical compound CCOCC#N WPYUCWSMVJJWFI-UHFFFAOYSA-N 0.000 claims description 2
- BPGIOCZAQDIBPI-UHFFFAOYSA-N 2-ethoxyethanamine Chemical compound CCOCCN BPGIOCZAQDIBPI-UHFFFAOYSA-N 0.000 claims description 2
- SNJNVEVAILOJBB-UHFFFAOYSA-N 2-ethoxypropanenitrile Chemical compound CCOC(C)C#N SNJNVEVAILOJBB-UHFFFAOYSA-N 0.000 claims description 2
- VBDBRROMHZXUIZ-UHFFFAOYSA-N 2-isocyanoethanamine Chemical compound NCC[N+]#[C-] VBDBRROMHZXUIZ-UHFFFAOYSA-N 0.000 claims description 2
- ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 claims description 2
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- PXXMSHBZYAOHBD-UHFFFAOYSA-N 3,3-diethoxypropan-1-amine Chemical compound CCOC(CCN)OCC PXXMSHBZYAOHBD-UHFFFAOYSA-N 0.000 claims description 2
- GTZVMEHLIMDKTK-UHFFFAOYSA-N 3,3-dimethylindole Chemical compound C1=CC=C2C(C)(C)C=NC2=C1 GTZVMEHLIMDKTK-UHFFFAOYSA-N 0.000 claims description 2
- DKLZNILLSAGSPK-UHFFFAOYSA-N 3-(3-isocyanopropoxymethyl)heptane Chemical compound CCCCC(CC)COCCC[N+]#[C-] DKLZNILLSAGSPK-UHFFFAOYSA-N 0.000 claims description 2
- LFFKXGFSDGRFQA-UHFFFAOYSA-N 3-(diethylamino)propanenitrile Chemical compound CCN(CC)CCC#N LFFKXGFSDGRFQA-UHFFFAOYSA-N 0.000 claims description 2
- MTPJEFOSTIKRSS-UHFFFAOYSA-N 3-(dimethylamino)propanenitrile Chemical compound CN(C)CCC#N MTPJEFOSTIKRSS-UHFFFAOYSA-N 0.000 claims description 2
- FLMYQHIFLGJJOP-UHFFFAOYSA-N 3-(isocyanomethyl)heptane Chemical compound CCCCC(CC)C[N+]#[C-] FLMYQHIFLGJJOP-UHFFFAOYSA-N 0.000 claims description 2
- SOYBEXQHNURCGE-UHFFFAOYSA-N 3-ethoxypropan-1-amine Chemical compound CCOCCCN SOYBEXQHNURCGE-UHFFFAOYSA-N 0.000 claims description 2
- NEXGYFPJGTWVIO-UHFFFAOYSA-N 3-isocyanopropan-1-amine Chemical compound NCCC[N+]#[C-] NEXGYFPJGTWVIO-UHFFFAOYSA-N 0.000 claims description 2
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 claims description 2
- DVGXDSPMPDANGA-UHFFFAOYSA-N 4-(9h-fluoren-1-yl)aniline Chemical compound C1=CC(N)=CC=C1C1=CC=CC2=C1CC1=CC=CC=C12 DVGXDSPMPDANGA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- WRDWWAVNELMWAM-UHFFFAOYSA-N 4-tert-butylaniline Chemical compound CC(C)(C)C1=CC=C(N)C=C1 WRDWWAVNELMWAM-UHFFFAOYSA-N 0.000 claims description 2
- IIADPZIQUFQWDZ-UHFFFAOYSA-N 7-isocyanoheptan-2-ylbenzene Chemical compound [C-]#[N+]CCCCCC(C)C1=CC=CC=C1 IIADPZIQUFQWDZ-UHFFFAOYSA-N 0.000 claims description 2
- SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 claims description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- DFNYGALUNNFWKJ-UHFFFAOYSA-N aminoacetonitrile Chemical compound NCC#N DFNYGALUNNFWKJ-UHFFFAOYSA-N 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 150000004982 aromatic amines Chemical class 0.000 claims description 2
- 125000005110 aryl thio group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 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
- 238000006243 chemical reaction Methods 0.000 claims description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- CAUSNBQXNXNCJC-UHFFFAOYSA-N ethanol cyanide Chemical compound [C-]#N.CCO.CCO CAUSNBQXNXNCJC-UHFFFAOYSA-N 0.000 claims description 2
- 125000005191 hydroxyalkylamino group Chemical group 0.000 claims description 2
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- KYCGURZGBKFEQB-UHFFFAOYSA-N n',n'-dibutylpropane-1,3-diamine Chemical compound CCCCN(CCCC)CCCN KYCGURZGBKFEQB-UHFFFAOYSA-N 0.000 claims description 2
- UDGSVBYJWHOHNN-UHFFFAOYSA-N n',n'-diethylethane-1,2-diamine Chemical compound CCN(CC)CCN UDGSVBYJWHOHNN-UHFFFAOYSA-N 0.000 claims description 2
- CSSDQXSEEDJINF-UHFFFAOYSA-N n,n-diethyl-3-isocyanopropan-1-amine Chemical compound CCN(CC)CCC[N+]#[C-] CSSDQXSEEDJINF-UHFFFAOYSA-N 0.000 claims description 2
- HNVKGVPNUGRUMP-UHFFFAOYSA-N naphthalene cyanide Chemical compound [C-]#N.C1=CC=CC2=CC=CC=C12 HNVKGVPNUGRUMP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 claims description 2
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 claims description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- QKPVEISEHYYHRH-UHFFFAOYSA-N 2-methoxyacetonitrile Chemical compound COCC#N QKPVEISEHYYHRH-UHFFFAOYSA-N 0.000 claims 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims 2
- 210000004268 dentin Anatomy 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- LGXXWLWXVYIODS-UHFFFAOYSA-N n-methyl-6-phenylhexan-1-amine Chemical compound CNCCCCCCC1=CC=CC=C1 LGXXWLWXVYIODS-UHFFFAOYSA-N 0.000 claims 2
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 claims 2
- SGIKAVNBVLFQSG-UHFFFAOYSA-N 1,1-diethyl-2,2-dimethylhydrazine Chemical compound CCN(CC)N(C)C SGIKAVNBVLFQSG-UHFFFAOYSA-N 0.000 claims 1
- UYHQUNLVWOAJQW-UHFFFAOYSA-N 1,3-benzothiazole-2-carbonitrile Chemical compound C1=CC=C2SC(C#N)=NC2=C1 UYHQUNLVWOAJQW-UHFFFAOYSA-N 0.000 claims 1
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- ZINJLDJMHCUBIP-UHFFFAOYSA-N ethametsulfuron-methyl Chemical compound CCOC1=NC(NC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC)=N1 ZINJLDJMHCUBIP-UHFFFAOYSA-N 0.000 description 1
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- ZPEPWSSGBIABSZ-UHFFFAOYSA-N isoindol-1-imine Chemical compound C1=CC=C2C(=N)N=CC2=C1 ZPEPWSSGBIABSZ-UHFFFAOYSA-N 0.000 description 1
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical group O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
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- 208000026451 salivation Diseases 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
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- 238000005507 spraying Methods 0.000 description 1
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- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 description 1
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- 229910052725 zinc 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/12—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted in position 3 and unsubstituted in position 7
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/03—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/04—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/06—Cobalt compounds
- C07F15/065—Cobalt compounds without a metal-carbon linkage
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/0091—Methine or polymethine dyes, e.g. cyanine dyes having only one heterocyclic ring at one end of the methine chain, e.g. hemicyamines, hemioxonol
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
- C09B23/04—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups one >CH- group, e.g. cyanines, isocyanines, pseudocyanines
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- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/10—The polymethine chain containing an even number of >CH- groups
- C09B23/105—The polymethine chain containing an even number of >CH- groups two >CH- groups
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- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0029—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only nitrogen as heteroatom
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0074—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B44/00—Azo dyes containing onium groups
- C09B44/10—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/045—Special non-pigmentary uses, e.g. catalyst, photosensitisers of phthalocyanine dyes or pigments
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- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/085—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex substituting the central metal atom
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- C09B47/04—Phthalocyanines abbreviation: Pc
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Description
556186
五、發明說明( 本發明係有關Co-酞青錯合物及光吸收化合物於可錄光 學資料媒趙之資料層中的用途(其中該資料層為光可錄光 學資料媒體)及彼等之製造方法。 唯錄式光碟(CD-R)近年來在量上已大為成長。資料層 5中之光吸收化合物代表光學資料媒體之一實體元件且必須 符合相當高度且多變的要求。雖然不是很稀有,但此種化 合物之製備是相當複雜的(參見WO-A-00/09522)。 因此,本發明之目的在於提供一種酞青染料,其可簡單 合成且符合用作在唯錄式光學資料媒體(主要是CD-R) 10 之資料層中之光吸收化合物的高度要求(諸如光安定性、 優異的信號/雜訊比、高記錄靈敏度、基質材料之無損害 塗覆等)。 令人驚詞1地,現已發現Co-敵青錯合物適合該目的。 本發明係有關一種光學資料媒體,其包含一種透明基質 15 ,該基質表面塗覆至少一種可錄資料層、視需要選用之反 射層、視需要選用之中間層及/或視需要選用之保護層, 其特徵在於光可錄資料層包含至少一種式I之Co-酞青錯 合物作為光吸收化合物: (請先閱讀背面之注意事項再填寫本頁) ·«----^----^訂---------線丨▲ 經濟部智慧財產局員工消費合作社印製 20 中其
p ㊉ 1 0 2 L· 11 · ο— 11 L w
[R
X R5] y 2 on
CoPc代表鈷(III)酞青, L1及L2為鈷中心原子之轴向對等鍵結配位基且基團R3 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 1L 2,000 556186 經濟部智慧財產局貝工消費合作社印製 A7 B7 五、發明說明(2 ) 至R6相當於酞青之取代基,其中 L1及L2互相獨立地代表式NR^RiR2之胺或代表式 … 〇 © 之異骑’ ΙΟΞΝ—R, 其中 5 R'R1及R2互相獨立地代表氫、烷基、環烷基、烯基、芳 基或雜芳基或基團RG至R2中之二者與彼等所鍵 結之N原子一起形成一氫化、部分氫化、倍半芳 香族或芳香族環,較佳為5-至7-員環,其選擇性 地包含其他雜原子,特別是來自由N、0及/或 10 S所組成之組群, R 代表烷基、環烷基、烯基、芳基或雜芳基, R3,R4,R5及R6互相獨立地代表鹵素、氰基、烷基、芳基、 烷胺基、二烷胺基、烷氧基、烷硫基、芳氧基、 芳硫基、S03H、S02NR7R8、C02R12、CONR7R8、 15 NH-COR12 或基團-(B)m_D, B 代表一橋員,選自一直接鍵、CH2、CO、CH(烷基)、 C(烷基)2、NH、S、O 或_CH=CH-,(B)m-代表橋 員B之化學上適宜之順序,其中m=l至10,較 佳 m=l、2、3 或 4, 20 D 代表下式之氧化還原系統之單價基團 X1-^CH=CH^Y-—— (還原) 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 (請先閱讀背面之注意事項再填寫本頁) «----Μ——:tr---------010,----------------------- 556186 A7 B7 五、發明說明(3 ) 或 θ X 士
ICH-CH ^2- (氧化) 經濟部智慧財產局貝工消費合作社印製 或代表茂金屬基團或茂金屬羰基基團,鈦、鎂、鐵、 釕或锇為適合作為金屬中心者, 5 X1及X2互相獨立地代表NRfIT、OR〃或SR", Y1 代表NRf、0或S,Y2代表NRh η 代表1至10且 R'及R〃互相獨立地代表氫、烷基、環烷基、芳基或雜芳基 或形成一直接鍵或一連至 10 鏈之一 C原子的架橋,一ch:^ w、x、y及z互相獨立地代表0至12,且w+x+y+z為$12, R7及R8互相獨立地代表烷胺基、羥基烷胺基、二烷胺基、 雙羥基烷胺基、芳胺基,或R7及R8與彼等所鍵結之 N原子一起形成一 5-、6-或7-員環,其選擇性地參有 15 其他雜原子,特別是來自由N、Ο及/或S所組成之 組群,NR7R8特別代表吡咯啶基、六氫吡啶或嗎咁基, R12代表烷基、芳基、雜芳基或氫, ArT代表一陰離子,特別代表鹵離子、Ci-至C20-烷基 COCT、曱酸鹽、草酸鹽、乳酸鹽、乙醇酸鹽、檸檬酸 20 鹽、CH30S03、NH2S03·、CH3S03·、ZSO/·或 1 /3P〇43-, 式I之Co-敵青錯合物亦可以式la的形式表示
R 11
CoPclR3] [R4] [R5] [R6] • w X y : (la) —5— (請先閱讀背面之注意事項再填寫本頁)
本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 A7 556186 _B7_ 五、發明說明(4 ) 其中
CoPc、L2、R3-R6基團及指數w、X、y和z具有如式(I) 之相同定義且 R11為鈷中心原子的共價鍵結基團且係衍生子一級或二級 5 胺或衍生自L1定義的異腈,亦即,代表-NRi2,R1 及R2具上述定義,或代表一CSN—R Αηθ Θ 惟,為簡化起見,下列陳述都與式(I)有關。但彼等當 然亦同樣適用於式(la)。 L1及L2定義中之較佳雜環胺配位基為嗎咁、六氫吡啶、 10 六氫吡畊、吡啶、2,2-聯吡啶、4,4-聯吡啶、嗒畊、嘧啶、 °比σ井、味嗤、苯并味嗤、異哼嗤、苯并異啐嗤、崎唆、苯 并σ夸0坐、嗔唾、苯并喧吐、4咐、吼洛、吲哚及3,3-二甲 基吲哚,彼等各自以氮原子與鈷原子配位。 烷基、烷氧基、芳基和雜環基可選擇性地攜帶其他基團 15 ,如烷基、函素、羥基、羥基烷基、胺基、烷胺基、二烷 胺基、硝基、氱基、CO-NH2、烷氧基、烷氧羰基、嗎啉基、 六氫吡啶基、吡咯啶基、吡咯啶酮基、三烷基甲矽基、三 烷基矽氧基或苯基。烷基和烷氧基團可為飽和、不飽和、 直鏈或支鏈的,烷基基團可為部分氫化或全氫化,且烷基 20 和烷氧基團可為乙氧化或丙氧化或甲矽化。於芳基或雜環 基團上之相鄰的烷基及/或烷氧基可一起形成三或四員架 橋。 較佳之式(I)化合物為那些就基團RG至R8及R、R、R〃 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) <請先閱讀背面之注意事項再填寫本頁)
— --I-----^ ^---------線 II 經濟部智慧財產局員工消費合作社印製 90. 11. 2,000 556186 A7 5 10 15 經濟部智慧財產局貝工消费合作社印製 20 發明說明(S) 及R12而言及就配位基LlL!而言,下述者 具有名稱“烷基,,之取代基較佳代表c r r ^ ^ 4 卜Cl6_燒基’特別是 CA烷基,其選擇性地被由素(如氣、漠或 疋 氰基及/或Ci-C6•烷氧基所取代; 、— 土 具有名稱“烷氧基,,之取代基較佳為C 0 r 〇 1 垸氧基,特別 疋CKV院氧基,其選擇性地被函素(如氣、漠 基、氰基及/或C]rC6-烷基所取代; 、— ! =名稱“魏基,’之取代基較佳代表^8_環烧基特 別疋CV至c6_環院基,其選擇性地被南素(如氣、漠或氣)、 經基、氛基及/或烷基所取代; 具有名稱“縣,,之取代練佳代表稀基,其選擇 性地被鹵素(如氣、溴或氟)、羥基、氰基及/或Ci_C6_ 烧基所取代,特別之稀基指的是烯丙基; 具有定義“雜芳基,,之取代基較佳代表具5_至7_員環之雜 環基團,其較佳包含雜原子,選自N、s及/或〇,且選 擇性地被稠合至芳香環或選擇性地攜帶其他取代基,例如 齒素、羥基、氰基及/或烷基,下列者特佳:吡啶基、呋 喊基、噻吩基、嘮唑基、噻唑基、咪唑基、喳咁基、苯并 畤唾基、苯并噻唑基及苯并咪唑基; 具有名稱“芳基,,之取代基較佳代表C6-C1(r芳基,特別是 苯基或萘基,其選擇性地被鹵素(如F、C1)、羥基、Ci-C6-烧基、Ci-CV烷氧基、N02及/或CN所取代。 較佳之式⑴的Co_酞青錯合物為下列,其中: L1及L2互相獨立地代表氨、曱胺、乙胺、乙醇胺、丙胺、 —7— 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 X 297公嫠) 90. 11. 2,000 (請先閲讀背面之注意事項再填寫本頁) i 11 ^----Γ ----I-- 556186 A7 B7 五、發明說明(6 ) 異丙胺、丁胺、異丁胺、第三-丁胺、戊胺、第三-戊 胺、苄胺、曱基苯基己胺、胺基丙胺、胺基乙胺、3_ 二甲基胺基丙胺、3-二乙基胺基丙胺、二乙基胺基乙 胺、二丁基胺基丙胺、嗎咁基丙胺、六氫吡啶基丙胺、 5 吡咯啶基丙胺、吡咯啶酮基丙胺、3-(甲基_羥基乙基 胺基)丙胺、曱氧基乙胺、乙氧乙胺、甲氧丙胺、乙氧 丙胺、甲氧乙氧丙胺、3-(2-乙基己基氧基)丙胺、異丙 氧基異丙胺、二曱胺、二乙胺、二乙醇胺、二丙胺、 二異丙胺、二丁胺、二異丁胺、二_第三-丁胺、二戊 10 胺、二-第三-戊胺、雙(2-乙基己基)胺、雙(胺基乙基) 胺、雙(胺基丙基)胺、雙(二_甲基胺基丙基)胺、雙(二 乙基胺基丙基)胺、雙(二乙基-胺基乙基)胺、雙(二丁 · 基胺基丙基)胺、二(嗎咁基-丙基)胺、二(六氫吡啶基 丙基)胺、二(吡咯啶基丙基)胺、二(吡咯啶酮基丙基) 15 胺、雙(3-(甲基-羥基乙基胺基)丙基)胺、二曱氧基乙 經濟部智慧財產局貝工消费合作社印製 胺、二乙氧基乙胺、二曱氧基丙胺、二乙氧基丙胺、 二(曱氧乙氧乙基)胺、二(曱氧乙氧丙基)胺、雙(3-(2-乙基己基氧基)丙基)胺、^一(異丙乳基異丙基)胺、三丙 胺、二(甲氧乙氧乙基)胺、三(甲氧乙氧丙基)胺、二乙 20 基胺基乙基六氫吡畊、二丙基胺基乙基六氫吡畊、嗎 咁、六氫吡啶、六氫吡畊、吡啶胺基、2-噻唑胺、2_ 苯并噻唑胺、2_苯并哼唑胺、3_亞胺基異吲哚咁胺、 吡啶、丙基吡啶、丁基吡啶、2,2_聯吡啶、4,4_聯吡咬、 塔畊、哺咬、吡畊、咪嗤、苯并咪峻、異畤吐、苯并 90· 2,〇〇〇 (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公* ) 556186 五、發明說明(7) 異十坐"号唾、苯并十坐、嗔唾、苯并嗔吐、啥咐、 比$ 、3,3·二甲基啊、’胺基吼唆、苯胺、對- 甲苯胺、對β第三丁基苯胺、對·曱氧苯胺基、異丙基 本fe、丁氧基笨胺或萘基胺, 或 10 15 經濟部智慧財產局員工消費合作社印製 20 L1及L2互相獨立地代表甲異猜、乙異腊、乙醇異赌、丙異 月青、異丙基異腈、丁異骑、異丁異赌、第三·丁基異精、 戍基異腈、第三-戊基異腈、午異腊、甲基苯基己基異 猜、胺基丙異腈、胺基乙異腈、3-二甲基胺基丙異骑、 3-二乙基胺基丙異腈、二乙基胺基乙異腈、二丁基胺 基丙異腈、嗎啉基丙異腈、六氫吡啶基丙異腈、吡咯 啶基丙異腈、吡咯啶酮基丙異腈、(甲基-羥基乙基 胺基)丙異腈、曱氧基乙異腈、乙氧基乙異腈、甲氧基 丙異腈、乙氧基丙異腈、甲氧基乙氧基丙異腈、3-(2-乙基己基氧基)丙異腈、異丙氧基異丙異腈、二甲異 腈、二乙異腈、二乙異腈、二乙醇異腈、二丙異腈、 二異丙異腈、二丁異腈、二異丁異腈、二-第三_丁異 腈、二戊異腈、二_第三·戊異腈、雙(2_乙基己基)異腈、 雙(胺基乙基)異腈、雙(胺基丙基)異腈、雙(二-甲基胺 基丙基)異腈、雙(二乙基胺基丙基)異腈、雙(二乙基_ 胺基乙基)異腈、雙(二丁基胺基丙基)異腈、二(嗎啉基 •丙基)異精、二(六氮吼咬基丙基)異猜、二(σ比洛咬基 丙基)異腈、二(吡咯啶酮基丙基)異腈、雙(3-(甲基-羥 基乙基胺基)丙基)異腈、二甲氧基乙異腈、二乙氧基 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 χ 297公釐) 90. 11. 2,000 (請先閲讀背面之注意事項再填寫本頁) —— — — — — II « — — — — — — I— —^^^1 — — — — — — —— — — — — — III — — — — — — · 556186 Α7
五、發明說明(8 ) 乙異腈、二甲氧基丙異腈、二乙氧基丙異腈、二(甲氧 基乙氧基乙基)異腈、二(曱氧基乙氧基丙基)異腈、雙 (3_(2_乙基己基氧基)丙基)異腈、二(異丙氧基異丙基) 異腈、三丙異腈、三(甲氧基乙氧基乙基)異腈、三(曱 5 氧基乙氧基丙基)異腈、二乙基胺基乙基六氫吡畊、二 丙基胺基乙基六氫吡畊、嗎咁、六氫吡啶、六氫吡畊、 吡啶胺基、2_噻唑異腈、2-苯并噻唑異腈、孓苯并啐 唑異腈、3_亞胺基異吲哚咁異腈、吡啶、丙基吡啶、 丁基吼咬、2,2-聯《»比咬、4,4-聯吼咬、疼σ井、咕咬、0比 10 畊、咪唑、苯并咪唑、異哼唑、苯并異噚唑、啐唑、 苯并σ号唾、喧峻、苯并喧嗤、咬咐、吼嘻、巧丨σ朵、3,3_ 二曱基吲哚,胺基吡啶、苯異腈、對_曱苯異勝、對_ 第三·丁基苯異腈、對-甲氧基苯異腈、異丙基苯異腈、 丁氧基苯異腈或萘異腈, 15 R3,R4,R5及R6互相獨立地代表氣、氟、溴、硬、氰基、 曱基、乙基、丙基、異丙基、丁基、異丁基、第三_ 丁基、戊基、第三-戊基、羥基乙基、3-二曱基胺基丙 基、3-^一乙基胺基丙基、本基、對-第二-丁基苯基、 對_曱氧基苯基、異丙基苯基、三氟甲基笨基、萘基、 20 曱胺基、乙胺基、丙胺基、異丙胺基、丁胺基、異丁 胺基、第三-丁胺、戊胺基、第三-戊胺基、苄胺基、 甲基苯基己胺基、羥基乙胺基、胺基丙胺基、胺基乙 胺基、3_二甲基胺基丙胺基、3-二乙基胺基丙胺基、 二乙基胺基乙胺基、二丁基胺基丙胺基、嗎咁基丙胺 —10— (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消费合作社印製 訂---------線I®---------------------- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 556186 經濟部智慧財產局員工消费合作社印製 A7 B7___ 五、發明說明(9 ) 基、六氫吡啶基丙胺基、吡咯啶基丙胺基、吡咯啶酮 基丙胺基、3-(甲基-羥基乙基胺基)丙胺基、甲氧基乙 基胺基、乙氧乙胺基、曱氧丙胺基、乙氧丙胺基、甲 氧乙氧丙胺基、3-(2-乙基己基氧基)丙胺基、異丙氧丙 5 胺基、二曱胺基、二乙胺基、二乙醇胺基、二丙胺基、 二異丙胺基、二丁胺基、二異丁胺基、二-第三-丁胺 基、二戊胺基、二-第三_戊胺基、雙(2-乙基己基)胺基、 雙(胺基乙基)胺基、雙(胺基丙基)胺基、雙(二-甲基胺 基丙基)胺基、雙(二乙基胺基丙基)胺基、雙(二乙基_ 10 胺基乙基)胺基、雙(二丁基胺基丙基)胺基、二(嗎咐基 -丙基)胺基、二(六氫吡啶基丙基)胺基、二(吡咯啶基 丙基)胺基、二(吡咯啶酮基丙基)胺基、雙(3_(曱基-羥 基乙基胺基)丙基)胺基、二甲氧基乙胺基、二乙氧基 乙胺基、二曱氧基丙胺基、二乙氧基丙胺基、二(曱氧 15 乙氧乙基)胺基、二(甲氧乙氧丙基)胺基、雙(3-(2-乙基 己基氧基)丙基)jfec基、一(異丙氧基異丙基)胺基、甲氧 基、乙氧基、丙氧基、異丙氧基、丁氧基、異丁氧基、 第三-丁氧基、戊氧基、第三-戊氧基、曱氧乙氧基、 乙氧乙氧基、曱氧丙氧基、乙氧丙氧基、曱氧乙氧丙 20 氧基、3-(2-乙基己基氧基)丙氧基、甲硫基、乙硫基、 丙硫基、異丙硫基、丁硫基、異丁硫基、第三·丁硫基、 戊硫基、第三-戊硫基、苯基、甲氧苯基、三氟曱基苯 基、萘基、C02R12、CONR7R8、NH_COR12、S03H、 S02NR7R8或代表下式之基團: —11— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90· 11. 2,000 (請先閱讀背面之注意事項再填寫本頁) I Aw-----:----i訂---------線」 556186 A7 B7 五、發明說明(10 )
其中 1一〇〜 -ch2-o- ,*-C2H4-0- . iCH(CH3)〇 (B)m代表 〇 或 ~C―OCH- ^-c-OC2H4 , II 〇 II 〇 星號(*)表示連結到5-員環, 10 Μ代表Μη或Fe陽離子, w、X、y及z互相獨立地代表〇至8,且w+x+y+z為£12。 ArT代表氣離子、溴離子、氟離子、-至C2(r烷基COO·、 甲酸鹽、草酸鹽、乳酸鹽、乙醇酸鹽、檸檬酸鹽、 CH30S03-、NH2S03-、CH3S03-、ZSO/-或 ZPO?、 15 NR7R8代表胺基、甲胺基、乙胺基、丙胺基、異丙胺基、 丁胺基、異丁胺基、第三-丁胺、戊胺基、第三-戊胺 基、苄胺基、甲基苯基己胺基、2_乙基_1_己基胺基、 Μ基乙胺基、胺基丙胺基、胺基乙胺基、3 -二甲基胺 基丙胺基、3-二乙基胺基丙胺基、嗎啉基丙胺基、六 20 氫吼咬基丙胺基、吼洛咬基丙胺基、吼洛咬_基丙胺 基、3-(曱基-羥基乙基胺基)丙胺基、甲氧基乙基胺基、 乙氧乙胺基、甲氧丙胺基、乙氧丙胺基、曱氧乙氧丙 胺基、3-(2_乙基己基氧基)丙胺基、異丙氧異丙胺基、 一甲胺基、^一乙胺基、二丙胺基、二丙胺基、二異丙 —12— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) ί清先閲璜背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 -I ________訂---------線 ----------------------- 90. 11. 2,000 556186 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(11 ) 胺基、二丁胺基、二異丁胺基、二-第三-丁胺基、二 戊胺基、二-第三-戊胺基、雙(2-乙基己基)胺基、二羥 基乙基胺基、雙(胺基乙基)胺基、雙(胺基丙基)胺基、 雙(3-二甲基胺基丙基)胺基、雙(3-二乙基胺基丙基)胺 5 基、一(嗎咐基丙基)胺基、二(六虱σ比咬基丙基)胺基、 二(吡咯啶基丙基)胺基、二(吡咯啶酮基丙基)胺基、雙 (3-(曱基-經基乙基胺基)丙基)胺基、二甲氧基乙胺 基、二乙氧基乙胺基、二甲氧基丙胺基、二乙氧基丙 胺基、二(甲氧基乙氧丙基)胺基、雙(3-(2-乙基己基氧 10 基)丙基)胺基、二(異丙氧基異丙基)胺基、苯胺基、對 -曱苯胺基、對-第三-丁基苯胺基、對-甲氧苯胺基、異 丙基苯胺基或萘胺基或NR7R8代表吡咯啶酮基、六氫 吡啶基、六氫吡畊基或嗎咁基, R12代表氫、曱基、乙基、丙基、異丙基、丁基、異丁基、 15 第三-丁基、戊基、第三-戊基、苯基、對-第三-丁基苯 基、對-甲氧苯基、異-丙基苯基、對-三氟曱基苯基、 氣基苯基、秦基、4·11比咬基、2-β比咬基、2-啥咐基、 2-吡咯基或2-吲哚基, 可能地,烷基、烷氧基、芳基和雜環基可選擇性地攜帶 20 其他基團,如烷基、自素、羥基、羥基烷基、胺基、烷胺 基、二烷胺基、硝基、氰基、CO-NH2、烷氧基、烷氧羰基、 嗎咐基、六氫吼唆基、吼略咬基、吼洛唆_基、三院基曱 矽基、三烷基矽氧基或苯基;烷基和烷氧基團可為飽和、 不飽和、直鏈或支鏈的;烷基基團可為部分氫化或全氫化; —13— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 (請先閲讀背面之注意事項再填寫本頁) -> --------^-------------------------------- 經濟部智慧財產局貝工消费合作社印製 556186 A7 _ B7 五、發明說明(12) 烧基及/或烧氧基團可為乙氧化或丙氧化或甲砍化的;及 於芳基或雜環基困上之相鄰的烷基及/或烷氧基可一起形 成三或四員架橋。 在本申請案之内容中,氧化還原系統應瞭解特別意指描 5 述於Angew· Chem. 1978,p927及於近代化學主題,第92卷, ρ·1(1980)中之氧化還原系統。 對-伸苯基二胺、4嗔Π井、二氫__、聯比旋鹽 及喳喏二甲烷為較佳的。 該等對應於下式(lb)之式(I)Co錯合物 10 h2nr2
Co®Pc (S〇2NR7R8)(鹵素)cmo (烷氧基)〇-4 An 〇
• 0-4 /TLX • 2 (lb), H2NR2 其中 卤素 代表氣、溴或氟, 15 烷氧基代表烷氧基, R7和R8互相獨立且具有上述意義, Αηθ、CoPc和R2同樣具有上述意義, 為特佳的。 本發明亦有關式Ic化合物 20 h2nr2 9° Pc(S〇2NR7R8)(鹵素)(M〇 (烷氧基)(Μ Απ〇 :2 “ h2nr2 (ic) 其中 ’ 鹵素 代表氣、溴或氟, —14一 [本紙張尺度適用中國國豕標準(CNS)A4規格(21。X 297公釐) · '-- 90. 11. 2,000 (請先閱讀背面之注意事項再填寫本頁) — -----:----1訂---------線」 556186 A7 B7 _— 五、發明說明(13) 烧氧基代表選擇性經取代之crC6-烷氧基, R7和R8互相獨立且具有上述意義, 及其他取代基具有上述意義。 本發明亦有關一種製備式(Ic)化合物的方法,其特徵在 5於經式S〇2Nr7R8之磺醯胺基取代(其中R7和R8具有上 述意義)且選擇性地經自素及/或烷氧基取代之Co-酞青 錯合物被氧化且係與胺類L1及L2反應。 製備法之實施較佳係由選擇性經自素及/或烷氧基取代 之Co_酞青錯合物為原料,藉在50-130°Ct以氣磺酸及亞 10 硫酿氣之磺醢氣化,及與對應胺之反應,在室溫至l〇〇°c 下獲得在pH 8-12水中之醯胺。轴胺取代基之後續加入較 佳在氧化環境下,如氣或空氣,較佳為空氣,且在空氣的 情況下,則在過量胺的存在下,以已知方法實施(參見實 施例13)。在氣的情況下,係先進行氧化,然後添加胺。 15 除了式I化合物外,光可錄資料層特佳另包含至少一種 其他選擇性經取代,含或不含中心原子之酞青作為光吸收 化合物。 適合之中心原子為例如選自由Si、Zn、A卜Cu、Pd、Pt、 Au及Ag,特另,j是Cu及Pd所組成之組群中。 20 例如,描述於DE_A 19 925 712之經磺醯胺基-取代之Cu-
敵青錯合物為特佳的。特佳為式II ^(SO2-NH-A-NR9R10)x CliPc(⑼, \(S〇3H)y —15— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局R工消费合作社印製 寒-----^---”訂---------線-·-------- 90. 11. 2,000 556186 A7
5 10 其中 CuPc代表鋼酞青基圏, A :表選擇性經取代之直鍵或支鏈c2_c6•稀 烯、丙烯、丁烯、戊烯或已烯, 乙 R9及^互_立地代錢或各自為選擇性經 =支鏈W如甲基、乙基、丙基、丁基直 取二是經取代之繼基及未經 或RW’與彼等所鍵結u原子一起形成雜環5_ 或6-員環,其選擇性地包含其他雜原子,如s、N或 (請先閱讀背面之注意事項再填寫本頁) 15 經濟部智慧財產局員工消费合作社印製 20 代表2.0至4.0, y 代表0至1.5及 X和y之總數為2.0至4.0,較佳為2 5至4.0。 特佳之混合物的成分為對應於式(IIa)之式π者 CuPc-[S02NH_CH2CH2CH2N(CH2)3] (Ila), 其中 CuPc代表銅酞青基團。 如描述於EP-A-519 395中之磺醯胺基-或醯胺基-取代戈 敵青為適合作為其他較佳之額外的光吸收化合物。 在不同光吸收化合物之混合物的情況下,式(I)化合物戈 比例較佳為混合物之10至90%。 特佳為式⑴和(II)以10:90至90:10,較佳20:80至80:20 特佳40:60至60:40重量比的混合物。
X —16— — — ^----;訂·!-----·線丨▲ 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 556186 A7 B7 五、發明說明(15) 資料層亦可包含黏著劑、濕潤劑、安定劑、稀釋劑及感 應劑及其他除了光吸收化合物外的成分。 基材可由光學透明塑膠(其若需要業經表面處理)來製 造。較佳之塑膠為聚碳酸酯及聚丙稀酸酯以及聚環烯或聚 5 烯。 反射層可由經常被用作可錄光學資料媒體之任何金屬或 金屬合金所製造。適合之金屬或金屬合金可藉蒸氣沉積及 喷艘法予以塗覆,且包含例如金、銀、銅、銘及彼等互相 或與其他金屬之合金。 10 覆蓋反射層之可能保護層可由uv_熟化丙烯酸酯組成。 保護反射層之可能的中間廣(例如由氧化而來)同樣可 存在。 本發明進一步係有關一種製造根據本發明光學資料媒 體之方法,其特徵在於光可錄資料層係藉塗覆至少一種式 15 Ϊ之Co-酞青錯合物,選擇性地與適合之黏著劑、添加劑及 溶劑混合,予以塗覆至透明基材上,且進一步視情況被供 以一反射層,視情況選用之其他中間層及視情況選用之保 護層。 經濟部智慧財產局員工消费合作社印製 (請先閲讀背面之注意事項再填寫本頁) 基材以式I光吸收化合物之塗覆,係選擇性地混合其他 20染料、黏著劑及/或溶劑,較佳藉旋塗法予以實施。 塗覆時,式I之光吸收化合物較佳被溶解於一適合之溶 劑或溶劑混合物(含或不含添加物)中,使式丨化合物相 對每100重量份之溶劑,總計達1〇〇%或更低,如1〇至2〇 重量份。可錄光學資料層隨後被金屬化(反射層),較佳在 叫7— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297 -—------ 90. 11. 556186 經濟部智慧財產局貝工消费合作社印製 A7 B7 五、發明說明(16 ) 減壓下藉喷鍍或蒸氣沉積法進行,且隨後可被供以一保護 塗層(保護層)或供以另一基材或覆蓋層。具有半透明反 射層之多層排列亦有可能。 供以式I之光吸收化合物或彼等與添加物及/或黏著劑 5 和其他光吸收化合物之混合物之塗層用之溶劑或溶劑混合 物的選擇,一方面係根據彼等對式I光吸收化合物和其他 添加物之溶解度,另一方面係基於對基材有最小影響來選 擇。對基材具有很小影響之適合的溶劑為例如醇、醚、烴 類、画化烴類、烷氧醇類及酮類。此種溶劑的實例為甲醇、 10 乙醇、丙醇、2,2,3,3-四氟丙醇、丁醇、二丙酮醇、苄醇、 四氣乙烷、二氣乙烷、二乙醚、二丙醚、二丁醚、曱基第 三-丁醚、甲氧乙醇、乙氧乙醇、’1-曱基-2-丙_、曱乙酮、 4-羥基-4-甲基-2-戊烷、己烷、環己烷、乙基環己烷、辛烷、 苯、甲苯、及二甲苯。較佳之溶劑為烴及醇,因為彼等對 15 基材有最輕微的影響。 適合供可錄資料層用之添加劑為安定劑、濕潤劑、黏著 劑、稀釋劑及感應劑。 實施例: 下列製備實例說明根據本發明所使用之染料的製備。 20 實施例1 將115克之Co-酞青於室溫下加入1公升乾燥氣苯中。 通入16克氣並實施攪拌30分鐘。在以氮氣吹出,去除過 量的氣之後’逐滴添加90克3·(甲基-經基乙基)丙胺。在 —18— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 (請先閲讀背面之注意事項再填寫本頁) I -----r---i 訂---------線—▲ 556186 A7 B7 五、發明說明(17) 90°C下持續攪拌30分鐘並於冷卻至室溫之後進行抽氣過 濾。以1公升氣苯和1公升水進行沖洗並將所獲得之染料 於真空中乾燥。 獲得156克下式之染料
5 NH2(CH2)3N(CH3)CH2CH2〇H 0o®Pc Cl°
I
I
NH2(CH2)3N(CH3)CH2CH2〇H λ*Λ670 奈米(NMP)。 下列化合物以類似方,法製備,但藉等莫耳量之另一種胺 10 或異腈取代3_(曱基-羥基乙基)丙胺。 (請先閲讀背面之注意事項再填寫本頁) 經濟部智慧財產局貝工消費合作社印製 食施例 L1 和 L2 RJ-R6 λ AK 奈米(NMP) 2 H2N-(CH2)17 ch3 H 664 3 /~\ H2N(CH2)3—Ν Ο H 669 4 h2n(ch2)3n(ch3)2 H 668 5 h2n(ch2)3och2ch3 H 665 6 H2N—CH-CHr(OCH2 CH)3-NH2 ch3 ch3 H 666 7 H2N—CH-CHp (cH-CH2-0*3—H ch3 ch3 12 H 666 8 ch2ch3 h2n(ch2)3〇-ch2ch-(ch2)3ch3 H 667 9 H H 664 10 C=N—C(CH3)3 H 665 —19— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) ,言. Γ 良 90. 11. 2,000 556186 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(18) 實施例11 將80克之壬溴-氣-Co-酞青於室溫下加入1公升乾燥氣 苯中。通入5克氣並實施攪拌30分鐘。在以氮氣吹出,去 除過量的氣之後,逐滴添加28克3-(曱基-羥基乙基)丙胺。 5 在90°C下持續攪拌30分鐘並於冷卻至室溫之後進行抽氣 過濾。以1公升氣苯和1公升水進行沖洗並將所獲得之染 料於真空中乾燥。 獲得88克下式之染料 h2n(ch2)3n(ch3)ch2ch2〇h
1〇 ㊉ Pc _9(CI) cP
I H2N(CH2)3N(CH3)CH2CH2〇H λ*Λ684 奈米(NMP) 〇 下列化合物藉使用等莫耳量之另一種胺以類似方法製 備0 實施例 L1 及 L2 R3 R4 r5-r8 λ最大 奈米 (NMP) 12 甲氧基-乙氧基-丙胺 ΒΓ9 Cl H 685 13 3-二甲基-胺基丙基-胺 Βγ9 Cl H 684 15 實施例14 磺醯氣化 131克 之98.8%之鈷酞青在30分鐘内被加入至 394克 之98%氯磺酸中。在25分鐘内將批料加熱至119 20 °C,在119°C下攪拌4小時並冷卻至85°C,及在 —20— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 (請先閱讀背面之注意事項再填寫本頁) ·----J 訂---------線 I®------------------------ 556186 經濟部智慧財產局員工消费合作社印製 A7 B7 五、發明說明(19) 85-88°C下,於2小時内逐滴添加 120毫升之亞硫醯氣(至少98%);然後實施加熱90-92 °C,歷時20分鐘,在90-92°C下進行攪拌4小時, 然後進行攪拌直到達成室溫為止。 5 產量:802克熔體。 醯胺形成: 將381克之熔體卸出至 1700克的冰上。溫度=-5°C。將沉澱之磺醯氣立刻以抽氣 過濾掉,以 10 1000毫升之冰水清洗中和並徹底抽乾。潮濕的磺醯氣立刻 進行進一步處理。先加入 750克 的冰和 750毫升的冰水。於攪拌中迅速加入磺醯氣至此混合物 中。然後添加 15 39克 的3-二曱基胺基丙胺。隨之將混合物加熱至80 °C,歷時60分鐘。藉10%強度之NaOH溶液保 持pH在10.00。在80°C及pH 10.0下攪拌此試驗 又45分鐘。 於冷卻至室溫之後,以抽氣過濾並以1000毫升 20 的水分批進行水洗。 產量:126.00克 轴配位基的導入 將354克3_二曱基胺基丙胺和14克NH4C1在90°C下加 —21— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 (請先閱讀背面之注意事項再填寫本頁)
556186 A7 ____B7__ 五、發明說明(20) 熱1小時。於冷卻至室溫之後,添加247克之Co-酞青·四 磺酸基-3-二甲基胺基丙胺和1克CoCl2。然後通過空氣10 小時。將混合物添加至5公升的水中並過濾。將染料於真 空中乾燥。 5 獲得275克下式染料。 NH2(CH2)3N(CH3)2 έο® Pc (S〇2NH(CH2)3N(CH3)2)4 ci° 9
I NH2(CH2)3N(CH3)2 10 實施例15 罐醯氣化 勺 131克 之98.8%之銘敵青在30分鐘内被加入至 394克之98 %氣績酸中。在25分鐘内將批料加熱至H9 °C,在119°C下攪拌4小時並冷卻至85°C,及在 15 85-88 C下,於2小時内逐滴添加 線- 120毫升之亞硫醯氣(至少98%);然後實施加熱9〇_92 °C,歷時20分鐘,在90-92°C下進行攪拌4小時, 然後進行攪拌直到達成室溫為止。 經濟部智慧財產局貝工消费合作社印製 產量:802克熔體。 20 醯胺形成: 將381克之炼體卸出至 17㈧克的冰上。溫度=-5〇c。將沉澱之磺醢氣立刻以抽氣 過濾掉,以 1〇〇〇亳升之冰水清洗中和並徹底抽乾。潮濕的磺醯氣立刻 —22— 本紙張尺度適用中國^ 90. 11. 2,000 556186 5 54克 10 A7 五、發明說明(21 ) 進行進一步處理。先加人 750克 的冰和 750毫升的冰水。於攪拌中迅逮加入磺醯氣至此混合物 中。然後添加 的甲氧基乙氧基丙胺。隨之將混合物加熱至8〇 °C ’歷時60分鐘。藉1〇%強度之Na〇ii溶液保 持PH在1〇·00。在80°C及pH 1〇.〇下持續攪拌 45分鐘。 於冷卻至室溫之後,以抽氣過濾並以1〇〇〇毫升 的水分批進行水洗。 產量:112克。 軸配位基的導入 199克Co-敵青-四確酸基_甲氧基乙氧基丙酿胺和 15 280克咪唑之混合物,以DMF補足到 1000毫升並在一開口燒瓶中攪拌24小時。將 1500毫升之水逐滴添加至此混合物中。過濾產物, 1〇〇〇毫升水清洗。將染料於真空中乾燥。 獲得197克下式染料 20 —23— 本紐尺度適財關(CNS)A4規格(21G x
(請先閱讀背面之注$項再填寫本頁)
556186 A7 B7 五、發明說明(22) 5
CoPc(S02NHCH2CH2CH2〇CH2CH2〇CH3)4 U λ*Λ670 奈米(NMP) 〇 (請先閱讀背面之注意事項再填寫本頁) - 10 實施例16 磺醯氣化 131克 之98.8%之鈷酞青在30分鐘内被加入至 288毫升之98%氣磺酸中。將混合物加熱至75°C,並在 75°C下攪拌4小時。於加熱至85°C之後,於2小 15 時内逐滴添加 120毫升之亞硫醯氣(至少98%)。在80°C下進行攪拌混 合物4小時,然後進行攪拌直到達成室溫為止。 產量:712克熔體。 醯胺形成: 20 將402克之熔體卸出至 1700克的冰上。將沉澱之磺醢氣立刻以抽氣過濾掉,以 1000毫升之冰水清洗中和並徹底抽乾。潮濕的磺醯氣立刻 進行進一步處理。先加入 7 5 0克 的冰和 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) j 訂---------手一 經濟部智慧財產局貝工消費合作社印製 90. 11. 2,000 556186 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(23) 750毫升的冰水。於攪拌中迅速加入磺醯氣至此混合物 中。然後添加 20克 的二異丁胺。隨之將混合物加熱至80°C,歷時 60分鐘。藉10%強度之NaOH溶液保持pH在 5 10.00。在80°C及pH 10.0下進行攪拌又45分鐘。 於冷卻至室溫之後,以抽氣過濾並以1000毫升 的水分批進行水洗。 將產物在真空中乾燥。 產量·· 95克。 10 轴配位基的導入 將354克3_二甲基胺基丙胺和14克NH4C1在90°C下加 熱1小時。於冷卻至室溫之後,添加219克之Co-酞青三 磺酸基二異丁基醯胺和1克CoCl2。然後通過空氣10小 15 時。將混合物添加至5公升的水中並過濾。將染料於真空 中乾燥。 獲得240克下式染料 NH2(CH2)3N(CH3)2 «
I
Co@ Pc (S〇2N(CH2)3CH(CH3)2)2 ci°
I
I
I 20 nh2(CH2)3n(ch3)2 λ狀 670 奈米(NMP) 〇 下列化合物藉使用等莫耳量之另一種胺L1或L2以類似 方法製備。 —25— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 ------------------------訂---------線! (請先閱讀背面之注意事項再填寫本頁) 556186 A7 B7 五、發明說明( 實施 例 L1 及 L2 R3 R4 R5 R6 R7 R8 λ最大 奈米 (ΝΜΡ) 17 3-二甲基-胺基丙 基-胺 so3h (S02NH- R7)3 H H 3-二甲基-胺基丙基 Η 671 18 甲氧基-乙氧基-丙胺 Βγ2 Cl4 so3h (S02N- R7R8)3 異丁基 異丁基 679 19 3-二甲基-胺基丙 基胺 (so2nh- r7)3 H H H 3-二甲基-胺基丙基 Η 672 (請先閱讀背面之注意事項再填寫本頁) 實施例20 32克3-(甲氧基乙氧基)酞腈和1-丁醇加熱至沸騰,添加 21克裡。在120°C下加熱此混合物1小時。於冷卻後,添 5 加500毫升水,並進行抽吸過濾。產量:15克染料。 金屬的導入: 將15克綠色染料添加至200毫升DMF中,並添加2克 CoCl2 〇將混合物迴流2小時。於冷卻後,添加2G0毫升水 10 進行抽氣過濾。產量:12克染料。 軸配位基的導入 經濟部智慧財產局員工消費合作社印製 將12克染料和24克咪唑之混合物於一開口燒瓶中以 200毫升之DMF授拌24小時。添加250毫升之水並進行 15 抽氣過濾。在真空中乾燥染料。獲得11克下式染料 —26— 90. 11. 2,000 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 556186 Α7 Β7 五、發明說明(25) 5 10
0 C
異構體混合物 (請先閲讀背面之注意事項再填寫本頁) λ 紅 715 奈米(NMP) 〇 以類似方法製備下列化合物: 15 經濟部智慧財產局員工消費合作社印製 -27— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 556186 A7 B7 五、發明說明(26) 實施例21 5 10
(請先閱讀背面之注意事項再填寫本頁) - · 15 經濟部智慧財產局員工消費合作社印製 20 λ*χ718 奈米(NMP) 〇 實施例22 在室溫下製備含等重量份之由實施例5而來之CoPc錯 合物和於2,2,3,3-四氟丙醇中之式Ila化合物之乾燥混合物 的2%強度溶液。藉旋塗法將此溶液塗覆至預先刻有溝槽 之聚碳酸酯基材。藉射出成形法將預先刻有溝槽之聚碳酸 酯製成圓盤。 圓盤的大小及溝槽結構與經常被用作CD-R者相當。具 有染料層作為資料載體之圓盤藉蒸氣沉積法被塗覆100奈 米之Ag。因此,藉旋塗法塗覆UV-熟化之丙烯酸酯塗層並 —28— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000 --線- 556186 經濟部智慧財產局貝工消费合作社印製 A7 B7____ 五、發明說明(27) 藉UV燈熟化。藉一商用CD-R測試燒錄機(Pulstec^OMT 2000 x 4),在資料讀取期間,例如在12 mW記錄電力及單 倍燒錄速度(1.4m/s)下,獲得3T信號之38%之調製高 度(30%至70%為CD-R規格)及11T信號之62%之調製 5 高度(>60%為CD-R規格)。 實施例23 在室溫下製備含等重量份之由實施例4而來之CoPc錯 合物和於2,2,3,3-四故丙醇中之式Ila化合物之乾燥混合物 10 的2%強度溶液。藉旋塗法塗覆此溶液。藉一商用CD-R 測試燒錄機(Pulstec® OMT 2000 X 4),在資料讀取期間, 例如在14 mW記錄電力及雙倍燒錄速度(2.8m/s)下, 獲得3T信號之32%之調製高度(30%至70%為CD-R規 格)及11T信號之68%調製高度(>60%為CD-R規格)。 15 實施例24 在室溫下製備含等重量份之由實施例4而來之Co-Pc錯 合物和於10%強度醋酸中之式na化合物之乾燥混合物的 32%強度溶液。類似實施例22藉旋塗法將此溶液塗覆至基 20 材上。並類似實施例20提供基材一反射層及保護層。然而 在一實施例20之改良中,僅塗覆50奈米之Ag作為反射 層。藉一商用CD-R測試燒錄機(PulstecOMT 2000 x 4), 在資料讀取期間,例如在8mW記錄電力及單倍燒錄速度 (I4m/S)下,獲得3T信號之32%之調製高度(30%至 —29— 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 9〇· 11· (請先閱讀背面之注意事項再填寫本頁) -訂------------- -n n ϋ n 556186 A7 B7 五、發明說明(28 ) 70%為CD-R規格)及11T信號之67%之調製高度(>60 %為CD-R規格)。 實施例25 5 在室溫下製備由實施例1而來於2,2,3,3-四氟丙醇中之 之Co敵青錯合物之2%溶液。類似實施例22藉旋塗法將 此溶液塗覆至基材上。並類似實施例20提供基材一反射層 及保護層。然而在一實施例20之改良中,僅塗覆50奈米 之Ag作為反射層。藉一商用CD-R測試燒錄機(Pulstec^ 10 OMT 2000 X 4),在資料讀取期間,例如在14 mW記錄電 力及單倍燒錄速度(1.4m/s)下,獲得3T信號之34%之 調製高度(30%至70%為CD-R規格)及11T信號之62 %調製高度(>60%為CD-R規格)。 經濟部智慧財產局具工消费合作社印製 ..#----U 訂---------線 |_---------------------- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 90. 11. 2,000
Claims (1)
- 556186 A8 B8 您2· 24修正 k、-請補梅 C8 D8 專利申請案第90123263號 ROC Patent Appln. No.90123263 修正之申請蕈利範圍中文本-附件(一) Amended Claims in Chinese ~ Encl.ri} ~~(民國92年2月M日送呈) (Submitted on February 2003) 10 1· 一種光學資料媒體,其包含一種透明基質,該基質表面 塗覆至少一種光可錄資料層、視需要選用之反射層、視 需要選用之中間層及/或視需要選用之保護層,其特徵 在於光可錄資料層包含至少一種式I之Co-欧青錯合物 作為光吸收化合物: 5 IX έο® Pc[R3] [R4] [R5] [R6] An0 ! w x y z L2 (I), 裝 計 其中 CoPc代表鈷(m)酞青,其中Li及L2為鈷中心原子之軸 向對等鍵結配位基且基團R3至R6相當於酞青之 取代基,其中 L1及L2互相獨立地代表式之胺或代表式0_® ^ ΙΟΞΝ—R, 之異腈,其中 R0, R1及R2互相獨立地代表氫、烷基、環烷基、烯基、 芳基或雜芳基或基團R〇:.‘至R2中之二者與彼等所 鍵結之N原子一起形成一氫化、部分氫化、倍半 芳香族或芳香族環,較佳為5-至7-員環,其選擇 性地包含其他雜原子,特別是來自由N、〇及/ 或S所組成之組群, -31 線 20 經濟部智慧財產局員工消費合作社印製 25 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 X 297公釐) 90434B-接 556186 A8 B8 C8 ------------D8 _ 六、申^iii -- R代表烷基、環烷基、烯基、芳基或雜芳基, r3, R4, R5及R6互相獨立地代表_素、氰基、烷基、芳 基、烷胺基、二烷胺基、烷氧基、烷硫基、芳氧 基 '芳硫基、S03H、S02NR7R8、co2r12、 5 CONR7R8、NH-COR12 或基團-(B)m〇, B代表一橋員,選自一直接鍵、CH2、CO、CH(烷 基)、C(烷基)2、NH、s、〇 或-CH=CH-,(B)m•代 表橋貝B之化學上適宜之順序,其中m=i至 10,較佳 m=l, 10 D代表下式之氧化還原系統之單價基團 X1~^CH—CH^Y· (還原) I, i 5 IX 經濟部智慧財產局員工消費合作社印製 20 或 ® © X^ZCH-CHJIIY—(氧化) 或代表茂金屬基團或茂金屬羰基基團,鈦、鎂、鐵、 釘或鐵為適合作為金屬中心者, X1及X2互相獨立地代表NR,R"、〇R〃或SR", γ1代表NR/、Ο或S, γ2代表NR/, n代表1至10且 化及R"互相獨立地代表氫、烷基、環烷基、芳基或雜芳 基或形成一直接鍵或一連至 鏈之一 C原子的架橋,一|CH二CH-)^或气CHsCH:^ w、X、y及Z互相獨立地代表〇至,且w+x+y+z為° t 绩 -32 - 556186 六 申請專利範圍 A8 B8 C8 D8 10 15 經濟部智慧財產局員工消費合作社印製 20 <12 ^ R7及R8互相獨立地代表烷胺基、羥基烷胺基、二烷胺 基、雙羥基烷胺基、芳胺基,或R7及R8與彼等 所鍵結之N原子一起形成一 5-、6-或7-員環,其 選擇性地參有其他雜原子,特別是來自由N、Ο 及/或S所組成之組群,NR7R8特別代表吡咯啶 基、六氫吡啶或嗎咁基, 代表烧基、芳基、雜芳基或氫, 代表一陰離子。 2·根據申請專利範圍第1項之光學資料媒體,其特徵在於 該光可錄資料層包含至少一種式I之Co-酞青錯合物, 其中就基團R0至R8, R,R,,R",R!2及就配位基L1及L2 而言,下述者為真: 具有名稱烧基之取代基較佳代表Ci_Ci6-烧基’特別是 CrCV烷基,其選擇性地被鹵素(如氣、溴或氟)、羥 基、氰基及/或CrC6-烷氧基所取代; 具有名稱“烷氧基,,之取代基較佳為CrC16-烷氧基,特別 是CrCV烧氧基,其選擇性地被鹵素(如氣、溴或 氟)、羥基、氰基及/或crc6-烷基所取代; 具有名稱“環烷基”之取代基較佳代表c4-c8-環烷基,特 別是CV至C6-環烧基,其選擇性地被鹵素(如氣、溴或 氟)、羥基、氰基及/或crc6-烷基所取代; 具有名稱“烯基”之取代基較佳代表c6-c8-烯基,其選擇 性地被齒素(如氣、溴或氟)、羥基、氰基及/或C1_ R12 Απ' -33 - 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 χ297公釐) 556186 A8 B8 C8 D8 六、申請專利範圍 CV烷基所取代,特別之烯基指的是稀丙基; 具有定義“雜芳基”之取代基較佳代表具5-至7-員環之雜 環基團,其較佳包含雜原子,選自N、S及/或0,且 選擇性地被稠合至芳香環或選擇性地攜帶其他取代基, 5 例如鹵素、羥基、氰基及/或烷基,下列者特佳: 11比咬基、吱喃基、喧吩基、喝ϋ坐基、σ塞α坐基、咪ϋ坐基、 喳唯基、苯并啐唑基、苯并噻唑基及苯并咪唑基;一 具有名稱“芳基”之取代基較佳代表C6-C1(r芳基,特別是 苯基或萘基,其選擇性地被鹵素(如F、C1)、羥基、 10 CrC6-烧基、Ci-C6-烧氧基、N〇2及/或CN所取代。 3·根據申請專利範圍第1項之光學資料媒體,其特徵在於 式I之CoPc錯合物對應於式lb h9nr2 i I Co®Pc (SO NR?R8)(鹵素)0-10 (统氧基)o-4 An 〇 15 : ? °-4 (Ib), h2nr2 其中取代基具有根據申請專利範圍第1項之定義。 4.根據申請專利範圍第1項之光學資料媒體,其特徵在於 經濟部智慧財產局員工消費合作社印製 光可錄資料層包含至少一種式I之Co-酞青錯合物,其 20 中 L1及L2互相獨立地代表氨、曱胺、乙胺、乙酵胺、丙 胺、異丙胺、丁胺、異丁胺、第三-丁胺、戊胺、 第三-戊胺、+胺、甲基苯基己胺、胺基丙胺、胺 基乙胺、3-二甲基胺基丙胺、3-二乙基胺基丙 -34 - 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公楚) 556186 Α8 Β8 C8 D8 六、申請專利範圍 胺、二乙基胺基乙胺、二丁基胺基丙胺、嗎啡基 丙胺、六氫吡啶基丙胺、吡咯啶基丙胺、吡咯啶 酮基丙胺、3-(曱基-羥基乙基胺基)丙胺、曱氧基 乙胺、乙氧乙胺、曱氧丙胺、乙氧丙胺、甲氧乙 5 氧丙胺、3-(2-乙基己基氧基)丙胺、異丙氧基異丙 胺、二甲胺、二乙胺、二乙醇胺、二丙胺、二異 丙胺、二丁胺、二異丁胺、二-第三-丁胺、二戊 胺、二-第三-戊胺、雙(2-乙基己基)胺、雙(胺基 乙基)胺、雙(胺基丙基)胺、雙(二-甲基胺基丙基) 10 胺、雙(二乙基胺基丙基)胺、雙(二乙基-胺基乙基) 胺、雙(二丁基胺基丙基)胺、二(嗎咁基-丙基) 胺、二(六氫吡啶基丙基)胺、二(吡咯啶基丙基) 胺、二(吡咯啶酮基丙基)胺、雙(3-(甲基-羥基乙 基胺基)丙基)胺、二甲氧基乙胺、二乙氧基乙 15 胺、二甲氧基丙胺、二乙氧基丙胺、二(甲氧乙氧 經濟部智慧財產局員工消費合作社印製 乙基)胺、二(甲氧乙氧丙基)胺、雙(3-(2-乙基己基 氧基)丙基)胺、二(異丙氧基異丙基)胺、三丙胺、 三(甲氧乙氧乙基)胺、三(曱氧乙氧丙基)胺、二乙 基胺基乙基六氫吡畊、二丙基胺基乙基六氫吡 20 畊、嗎咁、六氫吡啶、六氫吡畊、吡啶胺基、2- 噻唑胺、2-苯并噻唑胺、2-苯并啐唑胺、3-亞胺 基異⑼哚σ林胺、σ比淀、丙基σ比咬、丁基吼唆、 2,2-聯吼变、4,4-聯吼咬、洛喷、嘴唆、吼11 井、味 °坐、苯并咪唾、異4唾、苯并異4。坐、崎嗤、苯 -35 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 556186 A8 B8 C8 D8_ 六、申請專利範圍 并σ号α坐、σ塞σ坐、苯并嗔u坐、σ奎咐、σ比α各、ττ引哚、 3,3-二甲基吲哚,胺基吡啶、苯胺、對-甲苯胺、 對-第三-丁基苯胺、對-曱氧苯胺基、異丙基苯 胺、丁氧基苯胺或萘基胺,或 5 L·1及L·2互相獨立地代表曱異腈、乙異月旁、乙醇異猜、 丙異腈、異丙基異腈、丁異腈、異丁異腈、第三_ 丁基異腈、戊基異腈、第三-戊基異腈、苄異腈、 甲基苯基己基異腈、胺基丙異腈、胺基乙異腈、 3-二甲基胺基丙異腈、3-二乙基胺基丙異腈、二 10 乙基胺基乙異腈、二丁基胺基丙異腈、嗎咁基丙 異腈、六氫σ比咬基丙異腈、0比17各唆基丙異腈、°比 咯啶酮基丙異腈、3-(曱基-羥基乙基胺基)丙異 腈、甲氧基乙異腈、乙氧基乙異腈、甲氧基丙異 腈、乙氧基丙異腈、甲氧基乙氧基丙異腈、3-(2-15 乙基己基氧基)丙異腈、異丙氧基異丙異腈、二曱 經濟部智慧財產局員工消費合作社印製 異腈、二乙異腈、二乙異腈、二乙醇異腈、二丙 異腈、二異丙異腈、二丁異腈、二異丁異腈、二-第三-丁異腈、二戊異腈、二-第三-戊異腈、雙(2-乙基己基)異腈、雙(胺基乙基)異腈、雙(胺基丙基) 20 異腈、雙(二-曱基胺基丙基)異腈、雙(二乙基胺基 丙基)異腈、雙(二乙基-胺基乙基)異腈、雙(二丁 基胺基丙基)異腈、二(嗎咁基-丙基)異腈、二(六 氫吡啶基丙基)異腈、二(吡咯啶基丙基)異腈、二 (吡咯啶酮基丙基)異腈、雙(3_(曱基-羥基乙基胺 -36 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 8 8 8 8 A B c D 經濟部智慧財產局員工消費合作社印製 556186 六、申請專利範圍 基)丙基)異腈、二甲氧基乙異腈、二乙氧基乙異 腈、二曱氧基丙異腈、二乙氧基丙異腈、二(曱氧 基乙氧基乙基)異腈、二(曱氧基乙氧基丙基)異 腈、雙(3-(2-乙基己基氧基)丙基)異腈、二(異丙氧 5 基異丙基)異腈、三丙異腈、三(甲氧基乙氧基乙 基)異腈、三(曱氧基乙氧基丙基)異腈、二乙基胺 基乙基六氮0比。井、二丙基胺基乙基六氮11比σ井、嗎 咐、六氫σ比淀、六氫17比u井、吼咬胺基、2-嗔唾異 腈、2-苯并噻唑異腈、2-苯并哼唑異腈、3-亞胺 10 基異,σ朵σ林異腈、σ比咬、丙基σ比咬、丁基σ比咬、 2.2- 聯吼唆、4,4-聯吼咬、塔讲、嘴咬、吼咬、口米 唾、苯并咪唾、異噚唾、苯并異畤唾、畤哇、苯 并Π夸。坐、0塞ϋ坐、苯并σ塞H坐、Π奎Π林、π比洛、吲哚、 3.3- 二曱基吲哚,胺基吡啶、苯異腈、對-曱苯異 15 腈、對-第三-丁基苯異腈、對_甲氧基苯異腈、異 丙基苯異腈、丁氧基苯異腈或萘異腈, R3, R4, R5及R6互相獨立地代表氯、氟、溴、碘、氰 基、甲基、乙基、丙基、異丙基、丁基、異丁 基、第二-丁基、戊基、第二-戍基、經基乙基、 20 3-二曱基胺基丙基、3-二乙基胺基丙基、苯基、 對-第三-丁基苯基、對-甲氧基苯基、異丙基苯 基、三氟曱基苯基、萘基、曱胺基、乙胺基、丙 胺基、異丙胺基、丁胺基、異丁胺基、第三-丁 胺、戊胺基、第三-戊胺基、苄胺基、曱基苯基己 -37 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)556186 A8 B8 C8 D8_____ 夂、申請專利範圍 胺基、羥基乙胺基、胺基丙胺基、胺基乙胺基、 3-二甲基胺基丙胺基、3-二乙基胺基丙胺基、二 乙基胺基乙胺基、二丁基胺基丙胺基、嗎咁基丙 胺基、六氫吡啶基丙胺基、吡咯啶基丙胺基、吡 5 咯啶酮基丙胺基、3-(曱基-羥基乙基胺基)丙胺 基、曱氧基乙基胺基、乙氧乙胺基、甲氧丙胺 基、乙氧丙胺基、曱氧乙氧丙胺基、3-(2-乙基己 基氧基)丙胺基、異丙氧丙胺基、二甲胺基、二乙 胺基、二乙醇胺基、二丙胺基、二異丙胺基、二 10 丁胺基、二異丁胺基、二-第三-丁胺基、二戊胺 基、二-第三-戊胺基、雙(2_乙基己基)胺基、雙 (胺基乙基)胺基、雙(胺基丙基)胺基、雙(二-甲基 胺基丙基)胺基、雙(二乙基胺基丙基)胺基、雙(二 乙基-胺基乙基)胺基、雙(二丁基胺基丙基)胺基、 15 二(嗎咁基-丙基)胺基、二(六氫吡啶基丙基)胺 經濟部智慧財產局員工消費合作社印製 基、二(吡洛咬基丙基)胺基、二(吡洛咬酮基丙基) 胺基、雙(3-(甲基-羥基乙基胺基)丙基)胺基、二 曱氧基乙胺基、二乙氧基乙胺基、二曱氧基丙胺 基、二乙氧基丙胺基、二(甲氧乙氧乙基)胺基、 二(曱氧乙氧丙基)胺基、雙(3-(2-乙基己基氧基)丙 基)胺基、二(異丙氧基異丙基)胺基、甲氧基、乙 氧基、丙氧基、異丙氧基、丁氧基、異丁氧基、 第三-丁氧基、戊氧基、第三-戊氧基、曱氧乙氧 基、乙氧乙氧基、甲氧丙氧基、乙氧丙氧基、甲 556186 A8 B8 C8 D8 六、申請專利範圍 氧乙氧丙氧基、3-(2-乙基己基氧基)丙氧基、曱硫 基、乙硫基、丙硫基、異丙硫基、丁硫基、異丁 硫基、第三-丁硫基、戊硫基、第三-戊硫基、苯 基、甲氧苯基、三氟甲基苯基、萘基、C02R12、 5 CONR7R8、NH-COR12、S03H、S02NR7R8 或代表 下式之基團:經濟部智慧財產局員工消費合作社印製 其中 . * * ’、 —C-0—,*~CH2〇,^b2H4-0- , -CH(CH3)a 〇 (B)m 代表 *—c—oqh?—或 二〇c八, 15 Ο 〇 星號(*)表示連結到5-員環, w、X、y及ζ互相獨立地代表0至8,且w+x+y+z為 $12。 Απ' 代表氯離子、溴離子、氟離子、Cr至C2(r烷基 20 COO-、甲酸鹽、草酸鹽、乳酸鹽、乙醇酸鹽、 擰檬酸鹽、CH30S03·、NH2S03-、CH3S03·、 ZSO,或 ΧΡΟ?、 NR7R8代表胺基、曱胺基、乙胺基、丙胺基、異丙胺 基、丁胺基、異丁胺基、第三-丁胺、戊胺基、第 -39 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 556186 A8 B8 C8 D8 六、申請專利範圍 三戊胺基、辛胺基、甲基苯基己胺基、2-乙基-1-己基胺基、經基乙胺基、胺基丙胺基、胺基乙 胺基、3-二甲基胺基丙胺基、3-二乙基胺基丙胺 基、嗎咐基丙胺基、六氫咐^定基丙胺基、吼σ各唆 基丙胺基、吡咯啶酮基丙胺基、3-(甲基-羥基乙 基胺基)丙胺基、甲氧基乙基胺基、乙氧乙胺基、 甲氧丙胺基、乙氧丙胺基、甲氧乙氧丙胺基、3-(2-乙基己基氧基)丙胺基、異丙氧異丙胺基、二 甲胺基、二乙胺基、二丙胺基、二丙胺基、二異 丙胺基、二丁胺基、二異丁胺基、二-第三-丁胺 基、二戊胺基、二-第三-戊胺基、雙(2-乙基己基) 胺基、二羥基乙基胺基、雙(胺基乙基)胺基、雙 (胺基丙基)胺基、雙(3-二甲基胺基丙基)胺基、雙 (3-二乙基胺基丙基)胺基、二(嗎咁基丙基)胺基、 二(六氫吡啶基丙基)胺基、二(吡咯啶基丙基)胺 基、二(吡咯啶酮基丙基)胺基、雙(3-(甲基-羥基 乙基胺基)丙基)胺基、二曱氧基乙胺基、二乙氧 基乙胺基、二曱氧基丙胺基、二乙氧基丙胺基、 經 濟 部 智 慧 財 產 局 員 工 消 費 合 作 社 印 製 二(曱氧基乙氧丙基)胺基、雙(3-(2-乙基己基氧基) 丙基)胺基、二(異丙氧基異丙基)胺基、苯胺基、 對-曱苯胺基、對-第三-丁基苯胺基、對-甲氧苯 胺基、異丙基苯胺基或萘胺基或NR7R8代表吼洛 啶酮基、六氫吡啶基、六氫吡畊基或嗎啉基, R12 代表氫、曱基、乙基、丙基、異丙基、丁基、異 40 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 556186 A8 B8 C8 ____ D8______ 六、申請專利範圍 丁基、第三-丁基、戊基、第三-戊基、苯基、對_ 第三-丁基苯基、對-曱氧苯基、異-丙基苯基、 對-三氟甲基苯基、氰基苯基、萘基、4-吡啶基、 2-口比咬基、2-4咐基、2-ϋ比洛基或2-弓丨17朵基, 5 可能地,烷基、烷氧基、芳基和雜環基可選擇性地攜帶 其他基團,如烧基、鹵素、羥基、羥基烧基、胺基、烧 胺基、二烷胺基、硝基、氰基、C〇-NH2、烷氧基、烷 氧碳基、嗎咐基、六氫吼咬基、σ比洛咬基、吼H各咬_ 基、三烷基甲矽基、三烷基矽氧基或苯基;烷基和烷氧 10 基團可為飽和、不飽和、直鏈或支鏈的;烷基基團可為 部分氫化或全氫化;烷基及/或烷氧基團可為乙氧化或 丙氧化或甲矽化的;及於芳基或雜環基團上之相鄰的烷 基及/或烷氧基可一起形成三或四員架橋。 5·根據申請專利範圍第1項之光學資料媒體,其特徵在於 15 光可錄資料層另包含一種不同於⑴之含金屬或不含金屬 之献青,中心原子為例如選自由Si、Ζη、Α卜Cu、 Pd、Pt、Au及Ag,特別是Cu及Pd所組成之組群中。 經濟部智慧財產局員工消費合作社印製 6· —種包含可錄資料層之光學資料媒體,係藉利用波長 700至830奈米之光記錄在根據申請專利範圍第1項之 20 光學資料媒體上所獲得。 7· —種製備根據申請專利範圍第丨項之光學資料媒體的方 法,其特徵在於光可錄資料層係藉塗覆式I之Co_酞青 錯合物’選擇性地與適合之黏著劑、添加劑及適合溶劑 混合,予讀覆至透明紐± ’且視情況進—步被供以 -41 - ---------------- 本紙張尺度適用t國國家標準(CNS)A4規格(210x297公釐) ' 556186 六、申請專利範圍 A8 B8 C8 D8 一反射層,視情況翻之其他”層及視情況選 護層。 8· —種式Ic之化合物, 用之保 KNR之 9〇 Pc(S〇2NR7R8)(齒素)〇,(烷氧基)〇·4 An〇 H2NR" (Ic) 10 15 其中鹵素代表氣、漠或氣, R和R互相獨立且具有根據巾請專利範圍第1項中y 和R8之意義, 院”表選擇性經取代之〇1々烷氧基,& c々c、 An0'L1和L2具有根據申請專利範圍第丨項所述之意 義。 9·一種製備根據申請專利範圍第8項之化合物的方法,其 特徵在於經式S〇2NR7R8之磺醯胺基取代(其中R7和 R8具有上述意義)且選擇性地經鹵素及/或烷氧基取 代之Co_酞青錯合物被氧化且係與胺類。及L2反應。 經濟部智慧財產局員工消費合作社印製 -42 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)
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---|---|---|---|---|
US2756119A (en) * | 1948-10-29 | 1956-07-24 | Bayer Ag | Vat dyestuff composition |
DE1569753C3 (de) | 1967-08-31 | 1974-02-14 | Bayer Ag, 5090 Leverkusen | Komplexverbindungen der Kobaltphthalocyaninreihe |
US5248538A (en) | 1991-06-18 | 1993-09-28 | Eastman Kodak Company | Sulfonamido or amido substituted phthalocyanines for optical recording |
KR100288681B1 (ko) * | 1995-12-25 | 2001-05-02 | 나가시마 므쓰오 | 광 기록 재료 및 광 기록 매체 |
BR9912905A (pt) | 1998-08-11 | 2001-05-08 | Ciba Sc Holding Ag | Metalocenil-ftalocianinas |
JP3819293B2 (ja) | 1999-06-07 | 2006-09-06 | バイエル アクチェンゲゼルシャフト | 銅フタロシアニン色素を用いた光学式データ媒体 |
-
2001
- 2001-09-10 JP JP2002528765A patent/JP2004509377A/ja not_active Withdrawn
- 2001-09-10 AU AU2001285943A patent/AU2001285943A1/en not_active Abandoned
- 2001-09-10 CN CN01816124.3A patent/CN1283975C/zh not_active Expired - Fee Related
- 2001-09-10 PL PL36093901A patent/PL360939A1/xx not_active Application Discontinuation
- 2001-09-10 WO PCT/EP2001/010427 patent/WO2002025205A1/de not_active Application Discontinuation
- 2001-09-10 EP EP01965272A patent/EP1322906A1/de not_active Withdrawn
- 2001-09-10 CZ CZ2003832A patent/CZ2003832A3/cs unknown
- 2001-09-20 US US09/961,157 patent/US6713146B2/en not_active Expired - Fee Related
- 2001-09-21 TW TW090123263A patent/TW556186B/zh not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO2002025205A1 (de) | 2002-03-28 |
CZ2003832A3 (cs) | 2003-06-18 |
CN1462358A (zh) | 2003-12-17 |
US20020127366A1 (en) | 2002-09-12 |
JP2004509377A (ja) | 2004-03-25 |
US6713146B2 (en) | 2004-03-30 |
CN1283975C (zh) | 2006-11-08 |
AU2001285943A1 (en) | 2002-04-02 |
PL360939A1 (en) | 2004-09-20 |
EP1322906A1 (de) | 2003-07-02 |
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