JP4686136B2 - 蛍光材料 - Google Patents
蛍光材料 Download PDFInfo
- Publication number
- JP4686136B2 JP4686136B2 JP2004142143A JP2004142143A JP4686136B2 JP 4686136 B2 JP4686136 B2 JP 4686136B2 JP 2004142143 A JP2004142143 A JP 2004142143A JP 2004142143 A JP2004142143 A JP 2004142143A JP 4686136 B2 JP4686136 B2 JP 4686136B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- pyrazolin
- bis
- biphenyl
- benzene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 title description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 239000011888 foil Substances 0.000 claims description 2
- 229920001721 polyimide Polymers 0.000 description 27
- 239000009719 polyimide resin Substances 0.000 description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 10
- -1 pyrazoline compound Chemical class 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- UQLPVYMSIVODLN-UHFFFAOYSA-N 3-[4-[4-(2,5-diphenyl-3,4-dihydropyrazol-3-yl)phenyl]phenyl]-2,5-diphenyl-3,4-dihydropyrazole Chemical group C1C(C=2C=CC(=CC=2)C=2C=CC(=CC=2)C2N(N=C(C2)C=2C=CC=CC=2)C=2C=CC=CC=2)N(C=2C=CC=CC=2)N=C1C1=CC=CC=C1 UQLPVYMSIVODLN-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000007689 inspection Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229920005668 polycarbonate resin Polymers 0.000 description 6
- 239000004431 polycarbonate resin Substances 0.000 description 6
- 239000004642 Polyimide Substances 0.000 description 5
- 239000004305 biphenyl Substances 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 239000004020 conductor Substances 0.000 description 5
- 229920005575 poly(amic acid) Polymers 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 4
- 229940067157 phenylhydrazine Drugs 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- YSTSBXDVNKYPTR-UHFFFAOYSA-N 1-[4-(4-acetylphenyl)phenyl]ethanone Chemical group C1=CC(C(=O)C)=CC=C1C1=CC=C(C(C)=O)C=C1 YSTSBXDVNKYPTR-UHFFFAOYSA-N 0.000 description 2
- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 description 2
- HUNGHFQSKWSQGI-UHFFFAOYSA-N 5-[4-[4-(2,3-diphenyl-3,4-dihydropyrazol-5-yl)phenyl]phenyl]-2,3-diphenyl-3,4-dihydropyrazole Chemical group C1(=CC=CC=C1)N1N=C(CC1C1=CC=CC=C1)C1=CC=C(C=C1)C1=CC=C(C=C1)C1=NN(C(C1)C1=CC=CC=C1)C1=CC=CC=C1 HUNGHFQSKWSQGI-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000001640 fractional crystallisation Methods 0.000 description 2
- 238000004508 fractional distillation Methods 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- FXLOVSHXALFLKQ-UHFFFAOYSA-N p-tolualdehyde Chemical compound CC1=CC=C(C=O)C=C1 FXLOVSHXALFLKQ-UHFFFAOYSA-N 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PVRSIFAEUCUJPK-UHFFFAOYSA-N (4-methoxyphenyl)hydrazine Chemical compound COC1=CC=C(NN)C=C1 PVRSIFAEUCUJPK-UHFFFAOYSA-N 0.000 description 1
- SKBBQSLSGRSQAJ-UHFFFAOYSA-N 1-(4-acetylphenyl)ethanone Chemical compound CC(=O)C1=CC=C(C(C)=O)C=C1 SKBBQSLSGRSQAJ-UHFFFAOYSA-N 0.000 description 1
- HMIBQFXWSUBFTG-UHFFFAOYSA-N 1-[4-(diethylamino)phenyl]ethanone Chemical compound CCN(CC)C1=CC=C(C(C)=O)C=C1 HMIBQFXWSUBFTG-UHFFFAOYSA-N 0.000 description 1
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
- FGCZQOHSWGMVPN-UHFFFAOYSA-N 2,3,5-triphenyl-3,4-dihydropyrazole Chemical compound C1C(C=2C=CC=CC=2)N(C=2C=CC=CC=2)N=C1C1=CC=CC=C1 FGCZQOHSWGMVPN-UHFFFAOYSA-N 0.000 description 1
- XAFOTXWPFVZQAZ-UHFFFAOYSA-N 2-(4-aminophenyl)-3h-benzimidazol-5-amine Chemical compound C1=CC(N)=CC=C1C1=NC2=CC=C(N)C=C2N1 XAFOTXWPFVZQAZ-UHFFFAOYSA-N 0.000 description 1
- UVTILOYFTPJOEN-UHFFFAOYSA-N 2-[4-[2-[4-(1,3-benzothiazol-2-yl)phenyl]-5-[4-[2-[4-(1,3-benzothiazol-2-yl)phenyl]-3-[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-5-tert-butyl-1,3-benzoxazole Chemical compound CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)C4CC(=NN4C5=CC=C(C=C5)C6=NC7=CC=CC=C7S6)C8=CC=C(C=C8)C9=NN(C(C9)C1=CC=C(C=C1)C1=NC2=C(O1)C=CC(=C2)C(C)(C)C)C1=CC=C(C=C1)C1=NC2=CC=CC=C2S1 UVTILOYFTPJOEN-UHFFFAOYSA-N 0.000 description 1
- PDLRCZJIKSTRKB-UHFFFAOYSA-N 2-[4-[2-[4-(1,3-benzothiazol-2-yl)phenyl]-5-[4-[4-[2,3-bis[4-(1,3-benzothiazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-1,3-benzothiazole Chemical group C1C(N(N=C1C2=CC=C(C=C2)C3=CC=C(C=C3)C4=NN(C(C4)C5=CC=C(C=C5)C6=NC7=CC=CC=C7S6)C8=CC=C(C=C8)C9=NC1=CC=CC=C1S9)C1=CC=C(C=C1)C1=NC2=CC=CC=C2S1)C1=CC=C(C=C1)C1=NC2=CC=CC=C2S1 PDLRCZJIKSTRKB-UHFFFAOYSA-N 0.000 description 1
- XIDZGNGZCJKZOM-UHFFFAOYSA-N 2-[4-[2-[4-(1,3-benzoxazol-2-yl)phenyl]-3-[4-[2,5-bis[4-(1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-1,3-benzoxazole Chemical compound C1C(N(N=C1C2=CC=C(C=C2)C3=NC4=CC=CC=C4O3)C5=CC=C(C=C5)C6=NC7=CC=CC=C7O6)C8=CC=C(C=C8)C9CC(=NN9C1=CC=C(C=C1)C1=NC2=CC=CC=C2O1)C1=CC=C(C=C1)C1=NC2=CC=CC=C2O1 XIDZGNGZCJKZOM-UHFFFAOYSA-N 0.000 description 1
- SXMANFRWVNVEBN-UHFFFAOYSA-N 2-[4-[2-[4-(1,3-benzoxazol-2-yl)phenyl]-3-[4-[2-[4-(1,3-benzoxazol-2-yl)phenyl]-5-[4-(5-methyl-1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-5-methyl-1,3-benzoxazole Chemical compound CC1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)C4=NN(C(C4)C5=CC=C(C=C5)C6CC(=NN6C7=CC=C(C=C7)C8=NC9=CC=CC=C9O8)C1=CC=C(C=C1)C1=NC2=C(O1)C=CC(=C2)C)C1=CC=C(C=C1)C1=NC2=CC=CC=C2O1 SXMANFRWVNVEBN-UHFFFAOYSA-N 0.000 description 1
- BKALLXRLAFLKSW-UHFFFAOYSA-N 2-[4-[2-[4-(1,3-benzoxazol-2-yl)phenyl]-5-[4-[2,3-bis[4-(1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-1,3-benzoxazole Chemical compound C1C(N(N=C1C2=CC=C(C=C2)C3=NN(C(C3)C4=CC=C(C=C4)C5=NC6=CC=CC=C6O5)C7=CC=C(C=C7)C8=NC9=CC=CC=C9O8)C1=CC=C(C=C1)C1=NC2=CC=CC=C2O1)C1=CC=C(C=C1)C1=NC2=CC=CC=C2O1 BKALLXRLAFLKSW-UHFFFAOYSA-N 0.000 description 1
- JXNZZUUHFUJTTL-UHFFFAOYSA-N 2-[4-[2-[4-(1H-benzimidazol-2-yl)phenyl]-3-[4-[4-[2,5-bis[4-(1H-benzimidazol-2-yl)phenyl]-3,4-dihydropyrazol-3-yl]phenyl]phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-1H-benzimidazole Chemical group C1C(N(N=C1C2=CC=C(C=C2)C3=NC4=CC=CC=C4N3)C5=CC=C(C=C5)C6=NC7=CC=CC=C7N6)C8=CC=C(C=C8)C9=CC=C(C=C9)C1CC(=NN1C1=CC=C(C=C1)C1=NC2=CC=CC=C2N1)C1=CC=C(C=C1)C1=NC2=CC=CC=C2N1 JXNZZUUHFUJTTL-UHFFFAOYSA-N 0.000 description 1
- YDBOQJUZTSLQFK-UHFFFAOYSA-N 2-[4-[2-[4-(1H-benzimidazol-2-yl)phenyl]-5-[4-[2-[4-(1H-benzimidazol-2-yl)phenyl]-3-[4-(1,3-benzothiazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-1,3-benzothiazole Chemical compound C1C(N(N=C1C2=CC=C(C=C2)C3=NN(C(C3)C4=CC=C(C=C4)C5=NC6=CC=CC=C6S5)C7=CC=C(C=C7)C8=NC9=CC=CC=C9N8)C1=CC=C(C=C1)C1=NC2=CC=CC=C2N1)C1=CC=C(C=C1)C1=NC2=CC=CC=C2S1 YDBOQJUZTSLQFK-UHFFFAOYSA-N 0.000 description 1
- BZRWZFZGLWXPHE-UHFFFAOYSA-N 2-[4-[3-(4-methoxyphenyl)-5-[4-[3-(4-methoxyphenyl)-2-[4-(5-methyl-1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-3,4-dihydropyrazol-2-yl]phenyl]-5-methyl-1,3-benzoxazole Chemical compound CC1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)N4C(CC(=N4)C5=CC=C(C=C5)C6=NN(C(C6)C7=CC=C(C=C7)OC)C8=CC=C(C=C8)C9=NC1=C(O9)C=CC(=C1)C)C1=CC=C(C=C1)OC BZRWZFZGLWXPHE-UHFFFAOYSA-N 0.000 description 1
- AIFVOECCEFDXME-UHFFFAOYSA-N 2-[4-[3-(4-tert-butylphenyl)-5-[4-[4-[3-(4-tert-butylphenyl)-2-[4-(5-methyl-1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]phenyl]-3,4-dihydropyrazol-2-yl]phenyl]-5-methyl-1,3-benzoxazole Chemical group CC1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)N4C(CC(=N4)C5=CC=C(C=C5)C6=CC=C(C=C6)C7=NN(C(C7)C8=CC=C(C=C8)C(C)(C)C)C9=CC=C(C=C9)C1=NC2=C(O1)C=CC(=C2)C)C1=CC=C(C=C1)C(C)(C)C AIFVOECCEFDXME-UHFFFAOYSA-N 0.000 description 1
- HQYSFEHMUZBSHD-UHFFFAOYSA-N 2-[4-[3-[4-(1H-benzimidazol-2-yl)phenyl]-5-[4-[4-[3-[4-(1H-benzimidazol-2-yl)phenyl]-2-[4-(1,3-benzothiazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]phenyl]-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzothiazole Chemical group C1C(N(N=C1C2=CC=C(C=C2)C3=CC=C(C=C3)C4=NN(C(C4)C5=CC=C(C=C5)C6=NC7=CC=CC=C7N6)C8=CC=C(C=C8)C9=NC1=CC=CC=C1S9)C1=CC=C(C=C1)C1=NC2=CC=CC=C2S1)C1=CC=C(C=C1)C1=NC2=CC=CC=C2N1 HQYSFEHMUZBSHD-UHFFFAOYSA-N 0.000 description 1
- WAGXJBGNOUXCNH-UHFFFAOYSA-N 2-[4-[3-[4-[2,5-bis[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-3-yl]phenyl]-2-[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]-5-tert-butyl-1,3-benzoxazole Chemical compound CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)C4=NN(C(C4)C5=CC=C(C=C5)C6CC(=NN6C7=CC=C(C=C7)C8=NC9=C(O8)C=CC(=C9)C(C)(C)C)C1=CC=C(C=C1)C1=NC2=C(O1)C=CC(=C2)C(C)(C)C)C1=CC=C(C=C1)C1=NC2=C(O1)C=CC(=C2)C(C)(C)C WAGXJBGNOUXCNH-UHFFFAOYSA-N 0.000 description 1
- PYYIVXIZJOQBLH-UHFFFAOYSA-N 2-[4-[3-[4-[2-[4-(1,3-benzothiazol-2-yl)phenyl]-5-(4-ethoxyphenyl)-3,4-dihydropyrazol-3-yl]phenyl]-5-(4-ethoxyphenyl)-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzothiazole Chemical compound CCOC1=CC=C(C=C1)C2=NN(C(C2)C3=CC=C(C=C3)C4CC(=NN4C5=CC=C(C=C5)C6=NC7=CC=CC=C7S6)C8=CC=C(C=C8)OCC)C9=CC=C(C=C9)C1=NC2=CC=CC=C2S1 PYYIVXIZJOQBLH-UHFFFAOYSA-N 0.000 description 1
- RMBNIBGVIDNRAI-UHFFFAOYSA-N 2-[4-[3-[4-[2-[4-(1,3-benzothiazol-2-yl)phenyl]-5-(4-tert-butylphenyl)-3,4-dihydropyrazol-3-yl]phenyl]-5-(4-tert-butylphenyl)-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzothiazole Chemical compound CC(C)(C)C1=CC=C(C=C1)C2=NN(C(C2)C3=CC=C(C=C3)C4CC(=NN4C5=CC=C(C=C5)C6=NC7=CC=CC=C7S6)C8=CC=C(C=C8)C(C)(C)C)C9=CC=C(C=C9)C1=NC2=CC=CC=C2S1 RMBNIBGVIDNRAI-UHFFFAOYSA-N 0.000 description 1
- BIFHYLCYVPKIJO-UHFFFAOYSA-N 2-[4-[3-[4-[2-[4-(1,3-benzothiazol-2-yl)phenyl]-5-phenyl-3,4-dihydropyrazol-3-yl]phenyl]-5-phenyl-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzothiazole Chemical compound C1C(N(N=C1C2=CC=CC=C2)C3=CC=C(C=C3)C4=NC5=CC=CC=C5S4)C6=CC=C(C=C6)C7CC(=NN7C8=CC=C(C=C8)C9=NC1=CC=CC=C1S9)C1=CC=CC=C1 BIFHYLCYVPKIJO-UHFFFAOYSA-N 0.000 description 1
- NTSCHHRBRLXNBQ-UHFFFAOYSA-N 2-[4-[3-[4-[2-[4-(1,3-benzoxazol-2-yl)phenyl]-5-(4-ethoxyphenyl)-3,4-dihydropyrazol-3-yl]phenyl]-5-(4-ethoxyphenyl)-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzoxazole Chemical compound CCOC1=CC=C(C=C1)C2=NN(C(C2)C3=CC=C(C=C3)C4CC(=NN4C5=CC=C(C=C5)C6=NC7=CC=CC=C7O6)C8=CC=C(C=C8)OCC)C9=CC=C(C=C9)C1=NC2=CC=CC=C2O1 NTSCHHRBRLXNBQ-UHFFFAOYSA-N 0.000 description 1
- ZCUVVFKIDGCUKD-UHFFFAOYSA-N 2-[4-[3-[4-[2-[4-(1,3-benzoxazol-2-yl)phenyl]-5-(4-methylphenyl)-3,4-dihydropyrazol-3-yl]phenyl]-5-(4-methylphenyl)-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzoxazole Chemical compound CC1=CC=C(C=C1)C2=NN(C(C2)C3=CC=C(C=C3)C4CC(=NN4C5=CC=C(C=C5)C6=NC7=CC=CC=C7O6)C8=CC=C(C=C8)C)C9=CC=C(C=C9)C1=NC2=CC=CC=C2O1 ZCUVVFKIDGCUKD-UHFFFAOYSA-N 0.000 description 1
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- DAKHXVMGGIOTOU-UHFFFAOYSA-N 5-tert-butyl-2-[4-[5-[4-[4-[2-[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]-3-(4-methoxyphenyl)-3,4-dihydropyrazol-5-yl]phenyl]phenyl]-3-(4-methoxyphenyl)-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzoxazole Chemical group CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)N4C(CC(=N4)C5=CC=C(C=C5)C6=CC=C(C=C6)C7=NN(C(C7)C8=CC=C(C=C8)OC)C9=CC=C(C=C9)C1=NC2=C(O1)C=CC(=C2)C(C)(C)C)C1=CC=C(C=C1)OC DAKHXVMGGIOTOU-UHFFFAOYSA-N 0.000 description 1
- GXCSLQUOPDVOHN-UHFFFAOYSA-N 5-tert-butyl-2-[4-[5-[4-[4-[2-[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]-3-(4-methylphenyl)-3,4-dihydropyrazol-5-yl]phenyl]phenyl]-3-(4-methylphenyl)-3,4-dihydropyrazol-2-yl]phenyl]-1,3-benzoxazole Chemical group CC1=CC=C(C=C1)C2CC(=NN2C3=CC=C(C=C3)C4=NC5=C(O4)C=CC(=C5)C(C)(C)C)C6=CC=C(C=C6)C7=CC=C(C=C7)C8=NN(C(C8)C9=CC=C(C=C9)C)C1=CC=C(C=C1)C1=NC2=C(O1)C=CC(=C2)C(C)(C)C GXCSLQUOPDVOHN-UHFFFAOYSA-N 0.000 description 1
- NIJREGLYURVLSS-UHFFFAOYSA-N 5-tert-butyl-2-[4-[5-[4-[4-[3-[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]-2-phenyl-3,4-dihydropyrazol-5-yl]phenyl]phenyl]-2-phenyl-3,4-dihydropyrazol-3-yl]phenyl]-1,3-benzoxazole Chemical group CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)C4CC(=NN4C5=CC=CC=C5)C6=CC=C(C=C6)C7=CC=C(C=C7)C8=NN(C(C8)C9=CC=C(C=C9)C1=NC2=C(O1)C=CC(=C2)C(C)(C)C)C1=CC=CC=C1 NIJREGLYURVLSS-UHFFFAOYSA-N 0.000 description 1
- 0 CC(*1)=Nc2c1cc(*)cc2 Chemical compound CC(*1)=Nc2c1cc(*)cc2 0.000 description 1
- GURCXOHHXAMZOP-UHFFFAOYSA-N CCOC(C=C1)=CC=C1C(CC1C(C=C2)=CC=C2C2=CC=C(C(C3)N(C(C=C4)=CC=C4C4=NC(C=CC=C5)=C5N4)N=C3C(C=C3)=CC=C3OCC)C=C2)=NN1C(C=C1)=CC=C1C1=NC(C=CC=C2)=C2N1 Chemical group CCOC(C=C1)=CC=C1C(CC1C(C=C2)=CC=C2C2=CC=C(C(C3)N(C(C=C4)=CC=C4C4=NC(C=CC=C5)=C5N4)N=C3C(C=C3)=CC=C3OCC)C=C2)=NN1C(C=C1)=CC=C1C1=NC(C=CC=C2)=C2N1 GURCXOHHXAMZOP-UHFFFAOYSA-N 0.000 description 1
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- CZZGADHVBFGLCS-UHFFFAOYSA-N [3-(5-methyl-1,3-benzoxazol-2-yl)phenyl]hydrazine Chemical compound CC1=CC2=C(C=C1)OC(=N2)C3=CC(=CC=C3)NN CZZGADHVBFGLCS-UHFFFAOYSA-N 0.000 description 1
- ZVHOYFQNQJLWCI-UHFFFAOYSA-N [4-(1,3-benzothiazol-2-yl)phenyl]hydrazine Chemical compound C1=CC(NN)=CC=C1C1=NC2=CC=CC=C2S1 ZVHOYFQNQJLWCI-UHFFFAOYSA-N 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 150000001789 chalcones Chemical class 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- AFYCEAFSNDLKSX-UHFFFAOYSA-N coumarin 460 Chemical compound CC1=CC(=O)OC2=CC(N(CC)CC)=CC=C21 AFYCEAFSNDLKSX-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 229940015043 glyoxal Drugs 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
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000004031 phenylhydrazines Chemical class 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
- 238000010019 resist printing Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Description
R1およびR2は同一または異なり、水素原子、炭素数1〜8のアルキル基、
YはO、SもしくはNR3R4を示し、R3およびR4は同一または異なり、水素原子、炭素数1〜3のアルキル基を示し、
nは0、1または2を示す)
で表わされる高耐熱性ビスピラゾリン化合物および
R1およびR2は同一または異なり、水素原子、炭素数1〜8のアルキル基、
YはO、SもしくはNR3R4を示し、R3およびR4は同一または異なり、水素原子、炭素数1〜3のアルキル基を示し、
mは0または1を示し、
nは0、1または2を示す)
で表わされる高耐熱性ビスピラゾリン化合物に関する。
1,4−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−tert−オクチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−tert−ブチルスチリル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−エトキシフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−ジメチルアミノフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−スチリル−2−ピラゾリン−5−イル)ベンゼン、
4,4'−ビス(1−フェニル−3−スチリル−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−フェニル−3−(4−tert−ブチルフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−フェニル−3−(4−tert−ブチルスチリル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−フェニル−3−(4−ジメチルアミノフェニル)−2−ピラゾリン−5−イル)ビフェニル、
1,4−ビス(1−フェニル−3−(4−(ベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−3−(4−(ベンズイミダゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ベンゼン、
4,4'−ビス(1−フェニル−3−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−フェニル−3−(4−(ベンズチアゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ビフェニル、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−tert−ブチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−エトキシフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−(4−tert−ブチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−(4−メトキシフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−(4−ジメチルアミノフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−(4−tert−ブチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−(4−エトキジフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−(4−ジエチルアミノフェニル)−2−ピラゾリン−5−イル)ベンゼン
、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−3−(4−エトキシフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−3−(4−ジエチルアミノフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−3−(4−メトキシフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−3−(4−ジメチルアミノフェニル)−2−ピラゾリン−5−イル)ベンゼン、
4,4'−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−メトキシフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−ジメチルアミノフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−(4−エトキジフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−3−(4−ジエチルアミノフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−(4−メトキシフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−3−(4−ジメチルアミノフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−3−(4−tert−ブチルフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−3−(4−エトキシフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−3−(4−
エトキシフェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−3−(4−ジエチルアミノフェニル)−2−ピラゾリン−5−イル)ビフェニル、
1,4−ビス(1,3−ジ(4−(ベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1,3−ジ(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−3−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ベンゼン、
4,4'−ビス(1,3−ジ(4−(ベンズイミダゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1,3−ジ(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ビフェニル、
4,4'−ビス(1−(4−(メチルベンズオキサゾール−2−イル)フェニル)−3−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−5−イル)ビフェニル、
1−(1,3−ジフェニル−2−ピラゾリン−5−イル)−4−(1−フェニル−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ベンゼン、
1,4−ビス(1−フェニル−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−フェニル−5−(4−ジエチルアミノフェニル)−2−ピラゾリン−3−イル)ベンゼン、
4,4'−ビス(1,5−ジフェニル−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−フェニル−5−(4−メチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−フェニル−5−(4−tert−オクチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−フェニル−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−フェニル−5−(4−ジエチルアミノフェニル)−2−ピラゾリン−3−イル)ビフェニル、
1,4−ビス(1−フェニル−5−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−フェニル−5−(4−(ベンズチアゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ベンゼン、
4,4'−ビス(1−フェニル−5−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−フェニル−5−(4−(ベンズイミダゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ビフェニル、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−フェニル−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−(4−エトキシフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−(4−ジエチルアミノフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−(4−メチルフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−(4−ジメチルアミノフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−5−(4−エトキジフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−5−(4−ジエチルアミノフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−メチルフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−ジメチルアミノフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−フェニル−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−エトキシフェニル)−2−ピラゾリン−3−イル)ベンゼン、
4,4'−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−(4−メチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズオキサゾール−2−イル)フェニル)−5−(4−ジメチルアミノフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−フェニル−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−(4−エトキジフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−5−(4−ジエチルアミノフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−5−(4−メチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−フェニル−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−エトキシフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−ジメチルアミノフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−ジエチルアミノフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−メチルフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−ジメチルアミノフェニル)−2−ピラゾリン−3−イル)ビフェニル、
1,4−ビス(1,5−ジ(4−(ベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ベンゼン、
1,4−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−(ベンズチアゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ベンゼン、
4,4'−ビス(1,5−ジ(4−(ベンズチアゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1,5−ジ(4−(5−メチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズイミダゾール−2−イル)フェニル)−5−(4−(5−tert−ブチルベンズオキサゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ビフェニル、
4,4'−ビス(1−(4−(ベンズチアゾール−2−イル)フェニル)−5−(4−(ベンズイミダゾール−2−イル)フェニル)−2−ピラゾリン−3−イル)ビフェニル、および
1−(1−フェニル−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)−4−(1−フェニル−5−(4−メトキシフェニル)−2−ピラゾリン−3−イル)ベンゼン等が挙げられる。
R1およびR2は同一または異なり、水素原子、炭素数1〜8のアルキル基、
YはO、SもしくはNR3R4を示し、R3およびR4は同一または異なり、水素原子、炭素数1〜3のアルキル基を示す)
で表されるアセトフェノン類をエタノール−水混合溶液中、ピペリジン等の塩基性触媒存在下で縮合することにより、一般式(VI)
で表されるカルコン類の混合物を生成する。
R1およびR2は同一または異なり、水素原子、炭素数1〜8のアルキル基、
YはO、SもしくはNR3R4を示し、R3およびR4は同一または異なり、水素原子、炭素数1〜3のアルキル基を示す)
で表される化合物をエタノール−水混合溶液中、ピペリジン等の塩基性触媒存在下で縮合する以外は、一般式(I)の化合物と同様に製造することができる。
る。
苛性ソーダ9部を水15部に溶解し、エタノール250部を加え、撹拌する。これに4,4'−ジアセチルビフェニル23.8部およびベンズアルデヒド23.3部を懸濁したエタノール溶液を加え、20〜30℃で4時間撹拌する。析出物を濾別してフェニルヒドラジン18.5部を加え、氷酢酸400部中、110℃で3時間反応させた。室温まで冷却して得られた析出物を濾別、エタノールで精製して255〜286℃の融点を示す4,4'−ビス(1,5−ジフェニル−2−ピラゾリン−3−イル)ビフェニル 17.9部を得た。
苛性ソーダ9部を水15部に溶解し、エタノール150部を加え、撹拌する。これにテレフタルアルデヒド13.4部および4−アセチルトルエン32.2部を溶解したエタノール溶液を加え、20〜30℃で4時間撹拌する。析出物を濾別してフェニルヒドラジン23部を加え、氷酢酸600部中、115℃で3時間反応させた。室温まで冷却して得られた析出物を濾別、エタノールで精製して237〜264℃の融点を示す1,4−ビス(1−フェニル−3−(4−メチルフェニル)−2−ピラゾリン−5−イル)ベンゼン 20.8部を得た。
ポリイミド前駆共重合体(ポリアミック酸)溶液の調製
ピロメリット酸二無水物4.36g(0.02モル)および3,3’,4,4’−ベンゾフェノンテトラカルボン酸二無水物58.00g(0.18モル)のN−メチルピロリドン600ml溶液に6−アミノ−2−(p−アミノフェニル)ベンズイミダゾール44.86g(0.2モル)を30℃以下で仕込み、室温下で3時間攪拌し、ポリイミド前駆共重合体(ポリアミック酸)溶液707.2gを得た(固形分濃度15重量%)。得られた溶液は各67.0gに小分けして以下の実施例に適用した。
ポリアミック酸67.0gに、本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gを添加溶解し、ポリアミック酸に対して0.2%の蛍光剤含有の該溶液を得た。
このポリアミック酸溶液を、銅板上に焼成後厚みが所定の厚みになるようにキャストし、140℃で5分間熱風乾燥した後、350℃で10分間加熱してポリイミド共重合樹脂積層板を得、これをエッチング処理にて銅を除き、ポリイミド樹脂層を得た。得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gの代わりに、本発明の4,4'−ビス(1−フェニル−5−(4−tert−ブチルフェニル)−2−ピラゾリン−3−イル)ビフェニル0.02gを使用する以外はすべて実施例4と同様に行ない、ポリイミド樹脂層を得た。得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5
−イル)ビフェニル0.02gの代わりに、本発明の4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gを使用する以外はすべて実施例4と同様に行ない、ポリイミド樹脂層を得た。得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gの代わりに、本発明の4,4'−ビス(1−(4−(5−tret−ブチル−ベンゾオキサゾール−2−イル)フェニル)−3−フェニル−2−ピラゾリン−5−イル)ビフェニル0.02gを使用する以外はすべて実施例4と同様に行ない、ポリイミド樹脂層を得た。得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gの代わりに、1,5−ジフェニル−3−スチリル−2−ピラゾリン0.02gを使用する以外はすべて実施例4と同様に行ない、ポリイミド樹脂層を得た。得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gの代わりに、4−メチル−7−ジエチルアミノクマリン0.02gを使用する以外はすべて実施例4と同様に行ない、ポリイミド樹脂層を得た。得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gの代わりに、1,3,5−トリフェニル−2−ピラゾリン0.02gを使用する以外はすべて実施例1と同様に行ない、ポリイミド樹脂層を得た。
得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4の本発明の蛍光材料4,4'−ビス(1,3−ジフェニル−2−ピラゾリン−5−イル)ビフェニル0.02gの代わりに、1−(4−(5−tret−ブチル−ベンゾオキサゾール−2−イル)フェニル)−3−フェニル−5−tret−ブチルフェニル−2−ピラゾリン0.02gを使用する以外はすべて実施例4と同様に行ない、ポリイミド樹脂層を得た。
得られたポリイミド樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
実施例4〜実施例7に使用した本発明の各蛍光材料、および実施例8(比較例)〜実施例11(比較例)に使用した既知の各蛍光材料を、塩化ビニル樹脂に濃度0.2PHR(per hundred resin)で170℃にて通常練り込みを行ない、成型処理を施して樹脂層を得た。
得られた樹脂層は島津製作所製RF−540を用いて蛍光反射を測定した。
Claims (3)
- ポリイミド系樹脂またはポリカーボネート系樹脂上に金属箔を有する積層板において、該樹脂中に紫外〜可視短波長域に吸収を有する請求項1に記載の化合物および/または請求項2に記載の化合物を含有することを特徴とする積層板。
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US3527602A (en) * | 1967-08-31 | 1970-09-08 | Eastman Kodak Co | Organic photoconductors |
JPS57211154A (en) * | 1981-06-23 | 1982-12-24 | Canon Inc | Electrophotographic receptor |
JPS58214161A (ja) * | 1982-06-08 | 1983-12-13 | Canon Inc | 電子写真感光体 |
JPH05220894A (ja) * | 1992-02-07 | 1993-08-31 | Toshiba Chem Corp | 紫外線遮蔽性銅張積層板 |
JPH06184531A (ja) * | 1992-12-16 | 1994-07-05 | Nippon Kagaku Kogyosho:Kk | 蛍光材料 |
JPH10195131A (ja) * | 1996-12-24 | 1998-07-28 | Thomson Csf | 光重合性正孔注入ポリマー及び表示におけるその使用 |
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US3527602A (en) * | 1967-08-31 | 1970-09-08 | Eastman Kodak Co | Organic photoconductors |
JPS57211154A (en) * | 1981-06-23 | 1982-12-24 | Canon Inc | Electrophotographic receptor |
JPS58214161A (ja) * | 1982-06-08 | 1983-12-13 | Canon Inc | 電子写真感光体 |
JPH05220894A (ja) * | 1992-02-07 | 1993-08-31 | Toshiba Chem Corp | 紫外線遮蔽性銅張積層板 |
JPH06184531A (ja) * | 1992-12-16 | 1994-07-05 | Nippon Kagaku Kogyosho:Kk | 蛍光材料 |
JPH10195131A (ja) * | 1996-12-24 | 1998-07-28 | Thomson Csf | 光重合性正孔注入ポリマー及び表示におけるその使用 |
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