JP7477261B2 - ヒドロキシ化合物、その製造方法、樹脂組成物及びその硬化物 - Google Patents
ヒドロキシ化合物、その製造方法、樹脂組成物及びその硬化物 Download PDFInfo
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- JP7477261B2 JP7477261B2 JP2018064966A JP2018064966A JP7477261B2 JP 7477261 B2 JP7477261 B2 JP 7477261B2 JP 2018064966 A JP2018064966 A JP 2018064966A JP 2018064966 A JP2018064966 A JP 2018064966A JP 7477261 B2 JP7477261 B2 JP 7477261B2
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- Prior art keywords
- anhydride
- resin composition
- hydroxy compound
- group
- acid
- Prior art date
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- 150000002440 hydroxy compounds Chemical class 0.000 title claims description 35
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000011342 resin composition Substances 0.000 title description 20
- 239000003822 epoxy resin Substances 0.000 claims description 38
- 229920000647 polyepoxide Polymers 0.000 claims description 38
- 229920005989 resin Polymers 0.000 claims description 34
- 239000011347 resin Substances 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 32
- -1 phenol compound Chemical class 0.000 claims description 32
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 19
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 239000003377 acid catalyst Substances 0.000 claims description 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000002904 solvent Substances 0.000 description 24
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 23
- 238000006243 chemical reaction Methods 0.000 description 22
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 18
- 150000002989 phenols Chemical class 0.000 description 17
- 125000005462 imide group Chemical group 0.000 description 16
- 239000000463 material Substances 0.000 description 13
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 12
- 125000003277 amino group Chemical group 0.000 description 12
- 239000012435 aralkylating agent Substances 0.000 description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 11
- 238000005259 measurement Methods 0.000 description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- 150000008064 anhydrides Chemical class 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 8
- 239000005011 phenolic resin Substances 0.000 description 8
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 150000002430 hydrocarbons Chemical group 0.000 description 7
- 150000003949 imides Chemical group 0.000 description 7
- 229920003986 novolac Polymers 0.000 description 7
- 229920001568 phenolic resin Polymers 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- IMHDGJOMLMDPJN-UHFFFAOYSA-N biphenyl-2,2'-diol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1O IMHDGJOMLMDPJN-UHFFFAOYSA-N 0.000 description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 6
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 150000008065 acid anhydrides Chemical class 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 5
- 238000005538 encapsulation Methods 0.000 description 5
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 4
- FKBMTBAXDISZGN-UHFFFAOYSA-N 5-methyl-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1C(C)CCC2C(=O)OC(=O)C12 FKBMTBAXDISZGN-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 4
- 229940125782 compound 2 Drugs 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000011256 inorganic filler Substances 0.000 description 4
- 229910003475 inorganic filler Inorganic materials 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 150000003003 phosphines Chemical class 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 239000004848 polyfunctional curative Substances 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 150000003440 styrenes Chemical class 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- XPNGNIFUDRPBFJ-UHFFFAOYSA-N (2-methylphenyl)methanol Chemical compound CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 description 3
- KNDQHSIWLOJIGP-UMRXKNAASA-N (3ar,4s,7r,7as)-rel-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1,3-dione Chemical compound O=C1OC(=O)[C@@H]2[C@H]1[C@]1([H])C=C[C@@]2([H])C1 KNDQHSIWLOJIGP-UMRXKNAASA-N 0.000 description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- 229940018563 3-aminophenol Drugs 0.000 description 3
- VISOTGQYFFULBK-UHFFFAOYSA-N 3-hydroxy-4-phenylpyrrole-2,5-dione Chemical compound O=C1C(=O)NC(O)=C1C1=CC=CC=C1 VISOTGQYFFULBK-UHFFFAOYSA-N 0.000 description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 3
- IXCOKTMGCRJMDR-UHFFFAOYSA-N 9h-fluorene;phenol Chemical compound OC1=CC=CC=C1.OC1=CC=CC=C1.C1=CC=C2CC3=CC=CC=C3C2=C1 IXCOKTMGCRJMDR-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 229940125904 compound 1 Drugs 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- MUTGBJKUEZFXGO-UHFFFAOYSA-N hexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21 MUTGBJKUEZFXGO-UHFFFAOYSA-N 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical compound C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 3
- 229960001755 resorcinol Drugs 0.000 description 3
- 230000004580 weight loss Effects 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- HNASEWFYPPRNKM-UHFFFAOYSA-N 1-(methoxymethyl)-4-methylbenzene Chemical compound COCC1=CC=C(C)C=C1 HNASEWFYPPRNKM-UHFFFAOYSA-N 0.000 description 2
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 2
- RDNJCMOXCKTBNX-UHFFFAOYSA-N 2-(3,6-dihydroxy-2,4-dimethylphenyl)-3,5-dimethylbenzene-1,4-diol Chemical compound CC1=C(O)C(C)=CC(O)=C1C1=C(C)C(O)=C(C)C=C1O RDNJCMOXCKTBNX-UHFFFAOYSA-N 0.000 description 2
- HRVFQMNLCVAHMQ-UHFFFAOYSA-N 3-[2-[2-(2,3-dicarboxyphenyl)phenyl]sulfonyloxysulfonylphenyl]phthalic acid Chemical compound OC(=O)C1=CC=CC(C=2C(=CC=CC=2)S(=O)(=O)OS(=O)(=O)C=2C(=CC=CC=2)C=2C(=C(C(O)=O)C=CC=2)C(O)=O)=C1C(O)=O HRVFQMNLCVAHMQ-UHFFFAOYSA-N 0.000 description 2
- HDPBBNNDDQOWPJ-UHFFFAOYSA-N 4-[1,2,2-tris(4-hydroxyphenyl)ethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 HDPBBNNDDQOWPJ-UHFFFAOYSA-N 0.000 description 2
- YFQDXFWMFSQMMJ-UHFFFAOYSA-N 4-[2-[2-(3,4-dicarboxyphenyl)phenyl]sulfonyloxysulfonylphenyl]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C1=CC=CC=C1S(=O)(=O)OS(=O)(=O)C1=CC=CC=C1C1=CC=C(C(O)=O)C(C(O)=O)=C1 YFQDXFWMFSQMMJ-UHFFFAOYSA-N 0.000 description 2
- WFCQTAXSWSWIHS-UHFFFAOYSA-N 4-[bis(4-hydroxyphenyl)methyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 WFCQTAXSWSWIHS-UHFFFAOYSA-N 0.000 description 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
- OIGWAXDAPKFNCQ-UHFFFAOYSA-N 4-isopropylbenzyl alcohol Chemical compound CC(C)C1=CC=C(CO)C=C1 OIGWAXDAPKFNCQ-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
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- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 2
- 239000012346 acetyl chloride Substances 0.000 description 2
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- 239000000654 additive Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
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- 239000002585 base Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
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- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical compound C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
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- 229910052736 halogen Inorganic materials 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 150000002460 imidazoles Chemical class 0.000 description 2
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
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- 150000004780 naphthols Chemical class 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
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- 239000002798 polar solvent Substances 0.000 description 2
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 description 1
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- BXSZBTFVSMMJQG-UHFFFAOYSA-N naphtho[2,3-e][2]benzofuran-1,3-dione Chemical compound C1=CC2=CC3=CC=CC=C3C=C2C2=C1C(=O)OC2=O BXSZBTFVSMMJQG-UHFFFAOYSA-N 0.000 description 1
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Images
Description
(Z1およびZ2はそれぞれ独立して、水素原子または一価の置換基を表し、互いに結合して環を形成しても良い。破線部は、単結合または二重結合を表す。Aは式(a)で表されるアラルキル基を表し、nは1~3の数を表す。)
(ここで、R1およびR2は水素原子または炭素数1~6のアルキル基を示し、R3は水素原子または炭素数1~6の炭化水素基を示す。)
(ここで、Z1、Z2及び破線部は一般式(1)と同意である。)
(式中、R5は水素原子、水酸基、メチル基、メトキシ基またはハロゲン原子を示し、Xは直接結合、-O-、-S-、-SO2-、-CO-、または二価の炭素数1~12の炭化水素基を示す。mは1~10の数である。)
本発明のヒドロキシ化合物は、上記一般式(1)で表される。好ましいヒドロキシ化合物としては、上記一般式(2)で表される化合物がある。
一般式(1)において、Z1およびZ2はそれぞれ独立して、水素原子または一価の置換基を表し、互いに結合して環を形成しても良い。破線部は、単結合または二重結合を表す。Aは式(a)で表されるアラルキル基を表し、nは1~3の数を表す。式(a)において、R1およびR2は水素原子または炭素数1~6のアルキル基を示し、R3は水素原子または炭素数1~6の炭化水素基を示す。
本明細書中の化学式において、共通する記号は特に断りがない限り同じ意味を有する。
ここで、イミド基とは、下記式(b)で示される構造である。
M1及びM2は、それぞれ独立に、水素原子、C1~C12のアルキル基、フェニル基またはナフチル基である。また、M1、M2が結合して環を形成してもよい。好ましくは、M1とM2が結合して、N原子を含む5員環を形成する構造である。
式中、Z1およびZ2はそれぞれ独立して、水素原子または一価の置換基を表し、互いに結合して環を形成しても良い。破線部は、単結合または二重結合を表す。
Z1およびZ2が一価の置換基である場合は、好ましくは、アルキル基又はフェニル基であり、さらに好ましくはC1~C6のアルキル基又はフェニル基である。Z1およびZ2が結合して環を形成し、環状イミド基のイミド環と縮合環を形成する場合は、この環は好ましくはベンゼン環、シクロヘキセン環、ノルボルネン環、又はメチルノルボルネン環であり、上記縮合環はこれらがイミド環と縮合した構造の縮合環である。
(ここで、R3は水素原子又は炭素数1~6の炭化水素基を示し、R1およびR2は水素原子または炭素数1~6のアルキル基を示し、Xはハロゲン、OHまたはOR7を示し、R7は炭素数1~6のアルキル基を示す。)
電位差滴定装置を用い、1,4-ジオキサンを溶媒に用い、1.5mol/L塩化アセチルでアセチル化を行い、過剰の塩化アセチルを水で分解して0.5mol/L-水酸化カリウムを使用して滴定した。単位はg/eq.である。
1,4-ジオキサンを溶媒に用い、0.1M過塩素酸-酢酸溶液による電位差滴定により求めた。
示差走査熱量分析装(エスアイアイ・ナノテクノロジー株式会社製 EXSTAR6000 DSC/6200)により、昇温速度5℃/分の条件で、DSCピーク温度を求めた。すなわち、このDSCピーク温度を樹脂の融点とした。
BROOKFIELD製、CAP2000H型回転粘度計を用いて、150℃にて測定した。
本体(東ソー株式会社製、HLC-8220GPC)にカラム(東ソー株式会社製、TSKgelG4000HXL、TSKgelG3000HXL、TSKgelG2000HXL)を直列に備えたものを使用し、カラム温度は40℃にした。また、溶離液にはテトラヒドロフラン(THF)を使用し、1mL/分の流速とし、検出器は示差屈折率検出器を使用した。測定試料はサンプル0.1gを10mLのTHFに溶解し、マイクロフィルターで濾過したものを50μL使用した。データ処理は、東ソー株式会社製GPC-8020モデルIIバージョン6.00を使用した。
JIS-K-2207に従い環球法にて測定した。
質量分析計JMS-T100GCV(日本電子社製)を用いて測定した。試料をアセトンに溶解し、測定に供した。
熱機械測定装置(エスアイアイ・ナノテクノロジー株式会社製 EXSTAR6000TMA/6100)により、昇温速度10℃/分の条件でTgを求めた。
熱重量/示差熱分析装置(エスアイアイ・ナノテクノロジー製 EXSTAR6000TG/DTA6200、)を用いて、窒素雰囲気下、昇温速度10℃/分の条件において、5%重量減少温度(Td5)を測定した。また、700℃における重量減少を測定し、残炭率として算出した。無機フィラーを有する組成物の場合は、無機フィラーを除いた樹脂成分に換算することで、樹脂成分の残炭率を算出した。
誘電率及び誘電正接:IPC-TM-650 2.5.5.9に準じてマテリアルアナライザー(AGILENT Technologies社製)を用い、容量法により周波数1GHzにおける誘電率及び誘電正接を求めることにより評価した。
25℃、相対湿度50%の条件を標準状態とし、85℃、相対湿度85%の条件で100時間吸湿させた後の重量変化率とした。
1000mlの4口フラスコに、m‐アミノフェノール200.0g、トルエン50.0gを仕込み、窒素気流下、攪拌しながら110℃まで昇温し、4-メチルシクロヘキサン-1,2ジカルボン酸無水物323.9gを徐々に3時間かけて滴下し、10時間反応させた。この間、生成する水はトルエンとの共沸により系外に除き、トルエンは系内に戻した。反応後、水洗により過剰の酸無水物を除去し、トルエンと水を減圧留去して、淡褐色固体のフェノール化合物1を481.1g得た。そのフェノール化合物の水酸基当量は291であり、DSC測定結果におけるピーク温度は150℃であった。また、アミン当量が10万以上であり、アミノ基がほぼ全量反応していることを確認した。
1000mlの4口フラスコに、合成例1で得られたフェノール化合物300.0g、トルエン30.0gを仕込み、窒素気流下、撹拌しながら120℃まで昇温し、p-トルエンスルホン酸0.11gを加えた。次に、120℃にて撹拌しながらスチレン74.8gを3時間かけて滴下し反応させた。さらに、120℃にて3時間反応後、MIBK450gに溶解させ、80℃にて水洗を行い、MIBKを減圧留去することで、淡褐色固体のヒドロキシ化合物2を370g得た。このヒドロキシ化合物2の水酸基当量は378であり、軟化点は56℃であった。GPCチャートを図1に、FD-MSを図2に示す。一般式(1)におけるn=1成分が最も多く、n=2、n=3の成分を含むことが分かる。また、n=0成分を含み、nの平均値は約0.7と計算される。
溶剤溶解性の判定は、溶剤(メチルエチルケトン、トルエン、シクロペンタノン)5gに実施例1で得たヒドロキシ化合物2、合成例1で得たフェノール化合物1、およびN,N’‐ジフェニルメタンビスマレイミド(BMI;大和化成工業製)を、それぞれ固形分濃度で30重量%、50重量%、75重量%となるように投入し、室温下で十分に撹拌した後、不溶分を目視で確認した。不溶分がある場合を×、ない場合を〇とした。また、不溶分が確認されたものを60℃に加熱した際に不溶分の溶解が確認されたものを△とした。また、融点(mp)又は軟化点(sp)を測定した。結果を表1に示す。
エポキシ樹脂として、o-クレゾールノボラック型エポキシ樹脂(OCNE;エポキシ当量200、軟化点65℃)を用い、硬化剤成分として、合成例1で得たフェノール化合物1、合成例2で得たヒドロキシ化合物2、およびフェノールノボラック樹脂(PN;水酸基当量105、軟化点67℃)を用いた。硬化促進剤としてトリフェニルホスフィンを用い、表2に示す配合でエポキシ樹脂組成物を得た。表中の数値は配合における重量部を示す。このエポキシ樹脂組成物を用いて175℃にて成形し、175℃にて5時間ポストキュアを行い、硬化物試験片を得た後、各種物性測定に供した。
Claims (4)
- エポキシ樹脂及び硬化剤よりなるエポキシ樹脂組成物において、硬化剤の一部または全部として、請求項1に記載のヒドロキシ化合物の組成物を必須成分として含むことを特徴とするエポキシ樹脂組成物。
- 請求項3に記載のエポキシ樹脂組成物を硬化してなることを特徴とする樹脂硬化物。
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