JP4766856B2 - 酸素原子含有多環式化合物、重合性組成物及びその硬化物 - Google Patents
酸素原子含有多環式化合物、重合性組成物及びその硬化物 Download PDFInfo
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- JP4766856B2 JP4766856B2 JP2004251315A JP2004251315A JP4766856B2 JP 4766856 B2 JP4766856 B2 JP 4766856B2 JP 2004251315 A JP2004251315 A JP 2004251315A JP 2004251315 A JP2004251315 A JP 2004251315A JP 4766856 B2 JP4766856 B2 JP 4766856B2
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- Prior art keywords
- group
- oxabicyclo
- ring
- formula
- oxygen atom
- Prior art date
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- -1 polycyclic compound Chemical class 0.000 title claims description 100
- 125000004430 oxygen atom Chemical group O* 0.000 title claims description 57
- 239000000203 mixture Substances 0.000 title claims description 53
- 125000004432 carbon atom Chemical group C* 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 125000001424 substituent group Chemical group 0.000 claims description 25
- 150000002430 hydrocarbons Chemical group 0.000 claims description 23
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 23
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
- 125000002252 acyl group Chemical group 0.000 claims description 19
- 125000003277 amino group Chemical group 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 125000001188 haloalkyl group Chemical group 0.000 claims description 16
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 239000003505 polymerization initiator Substances 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 13
- 125000003367 polycyclic group Chemical group 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 11
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 10
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical group CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 claims description 10
- 125000004043 oxo group Chemical group O=* 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 125000000623 heterocyclic group Chemical group 0.000 claims description 9
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 8
- 125000006574 non-aromatic ring group Chemical group 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000001976 hemiacetal group Chemical group 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000004434 sulfur atom Chemical group 0.000 claims description 5
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 4
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 4
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 claims description 4
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- DKHYBELEERFQEU-UHFFFAOYSA-N 2-oxabicyclo[1.1.1]pentane Chemical group C1C2CC1O2 DKHYBELEERFQEU-UHFFFAOYSA-N 0.000 claims description 3
- ZQCZKNJMUNAGGK-UHFFFAOYSA-N 5-oxabicyclo[2.1.1]hexane Chemical group C1CC2CC1O2 ZQCZKNJMUNAGGK-UHFFFAOYSA-N 0.000 claims description 3
- KFZRLMPLQBLWMG-UHFFFAOYSA-N 6-oxabicyclo[3.1.1]heptane Chemical group C1CCC2CC1O2 KFZRLMPLQBLWMG-UHFFFAOYSA-N 0.000 claims description 3
- YPWFNLSXQIGJCK-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]heptane Chemical group C1CC2CCC1O2 YPWFNLSXQIGJCK-UHFFFAOYSA-N 0.000 claims description 3
- FQUMQEFEWGUVRR-UHFFFAOYSA-N 7-oxabicyclo[4.1.1]octane Chemical group C1CCCC2CC1O2 FQUMQEFEWGUVRR-UHFFFAOYSA-N 0.000 claims description 3
- AWEGTPPFDJUPRI-UHFFFAOYSA-N 8-oxabicyclo[3.2.1]octane Chemical group C1CCC2CCC1O2 AWEGTPPFDJUPRI-UHFFFAOYSA-N 0.000 claims description 3
- DDXPJVFYAZDUKM-UHFFFAOYSA-N 9-oxabicyclo[3.3.1]nonane Chemical group C1CCC2CCCC1O2 DDXPJVFYAZDUKM-UHFFFAOYSA-N 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims description 3
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- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
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- 230000008878 coupling Effects 0.000 claims description 2
- 238000010168 coupling process Methods 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 72
- 150000001875 compounds Chemical class 0.000 description 59
- 125000006239 protecting group Chemical group 0.000 description 25
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- 125000001931 aliphatic group Chemical group 0.000 description 11
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 11
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 9
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- 239000000463 material Substances 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 125000000962 organic group Chemical group 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 7
- 125000004122 cyclic group Chemical group 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
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- 238000006886 vinylation reaction Methods 0.000 description 7
- NVXPIXAOPDSGTR-UHFFFAOYSA-N 5-(hydroxymethyl)-7-oxabicyclo[2.2.1]heptan-3-ol Chemical compound C1C(O)C2C(CO)CC1O2 NVXPIXAOPDSGTR-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
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- 238000000926 separation method Methods 0.000 description 6
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 5
- SIZKKURETCQUKI-UHFFFAOYSA-N 9-oxabicyclo[3.3.1]nonane-2,6-diol Chemical compound O1C2C(O)CCC1C(O)CC2 SIZKKURETCQUKI-UHFFFAOYSA-N 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- FKTLISWEAOSVBS-UHFFFAOYSA-N 2-prop-1-en-2-yloxyprop-1-ene Chemical class CC(=C)OC(C)=C FKTLISWEAOSVBS-UHFFFAOYSA-N 0.000 description 4
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 4
- HYEIZNHBXAADMJ-UHFFFAOYSA-N 6-(hydroxymethyl)-3-methoxy-7-oxabicyclo[2.2.1]heptan-2-ol Chemical compound COC1C2CC(C(C1O)O2)CO HYEIZNHBXAADMJ-UHFFFAOYSA-N 0.000 description 4
- FUCCKJSLKAHDNQ-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]hept-2-en-5-ylmethanol Chemical compound O1C2C(CO)CC1C=C2 FUCCKJSLKAHDNQ-UHFFFAOYSA-N 0.000 description 4
- GJZQHDOUUCAZHY-UHFFFAOYSA-N 9-oxabicyclo[4.2.1]nonane-2,5-diol Chemical compound OC1CCC(O)C2CCC1O2 GJZQHDOUUCAZHY-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 206010040880 Skin irritation Diseases 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000003377 acid catalyst Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 3
- IJZNZJBPVWYGIL-UHFFFAOYSA-N 2,6-bis(ethenoxy)-9-oxabicyclo[3.3.1]nonane Chemical compound O1C2C(OC=C)CCC1C(OC=C)CC2 IJZNZJBPVWYGIL-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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- VQZIWHUGUSNZPW-UHFFFAOYSA-N 6-ethenoxy-9-oxabicyclo[3.3.1]nonan-2-ol Chemical compound OC1C2CCC(C(CC1)O2)OC=C VQZIWHUGUSNZPW-UHFFFAOYSA-N 0.000 description 3
- NPSBNWMHALOXRF-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]heptane Chemical group C1CC2CCC1O2.C1CC2CCC1O2 NPSBNWMHALOXRF-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 description 2
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- 125000000304 alkynyl group Chemical group 0.000 description 2
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- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- ZOAIGCHJWKDIPJ-UHFFFAOYSA-M caesium acetate Chemical compound [Cs+].CC([O-])=O ZOAIGCHJWKDIPJ-UHFFFAOYSA-M 0.000 description 1
- ZMCUDHNSHCRDBT-UHFFFAOYSA-M caesium bicarbonate Chemical compound [Cs+].OC([O-])=O ZMCUDHNSHCRDBT-UHFFFAOYSA-M 0.000 description 1
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 1
- 229910000024 caesium carbonate Inorganic materials 0.000 description 1
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- UVJHQYIOXKWHFD-UHFFFAOYSA-N cyclohexa-1,4-diene Chemical group C1C=CCC=C1 UVJHQYIOXKWHFD-UHFFFAOYSA-N 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004980 cyclopropylene group Chemical group 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002373 hemiacetals Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910021432 inorganic complex Inorganic materials 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 150000002504 iridium compounds Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M isovalerate Chemical compound CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000000686 lactone group Chemical group 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 229910000032 lithium hydrogen carbonate Inorganic materials 0.000 description 1
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 description 1
- HQRPHMAXFVUBJX-UHFFFAOYSA-M lithium;hydrogen carbonate Chemical compound [Li+].OC([O-])=O HQRPHMAXFVUBJX-UHFFFAOYSA-M 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 150000004972 metal peroxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical group C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 1
- UMRZSTCPUPJPOJ-KNVOCYPGSA-N norbornane Chemical compound C1C[C@H]2CC[C@@H]1C2 UMRZSTCPUPJPOJ-KNVOCYPGSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- RPDAUEIUDPHABB-UHFFFAOYSA-N potassium ethoxide Chemical compound [K+].CC[O-] RPDAUEIUDPHABB-UHFFFAOYSA-N 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 125000006410 propenylene group Chemical group 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 231100000438 skin toxicity Toxicity 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- WBQTXTBONIWRGK-UHFFFAOYSA-N sodium;propan-2-olate Chemical compound [Na+].CC(C)[O-] WBQTXTBONIWRGK-UHFFFAOYSA-N 0.000 description 1
- SIXNTGDWLSRMIC-UHFFFAOYSA-N sodium;toluene Chemical compound [Na].CC1=CC=CC=C1 SIXNTGDWLSRMIC-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- UIUWNILCHFBLEQ-NSCUHMNNSA-N trans-pent-3-enoic acid Chemical compound C\C=C\CC(O)=O UIUWNILCHFBLEQ-NSCUHMNNSA-N 0.000 description 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
本発明の他の目的は、硬化速度が速く、しかも硬度の高い硬化物を形成しうる酸素原子含有多環式化合物、これを含む重合性組成物及びその硬化物を提供することにある。
で表される基を示し、少なくとも1つは上記式(2)で表される基である。Wは(i)ヒドロキシル基、ヒドロキシメチル基、アミノ基、カルボキシル基、スルホ基、ハロゲン原子、オキソ基、シアノ基、ニトロ基、複素環式基、炭化水素基、及びハロアルキル基から選択される基で水素原子が置換されていてもよい2価の炭化水素基、(ii)ヒドロキシル基、ヒドロキシメチル基、アミノ基、カルボキシル基、スルホ基、ハロゲン原子、オキソ基、シアノ基、ニトロ基、複素環式基、炭化水素基、及びハロアルキル基から選択される基で水素原子が置換されていてもよい2価の炭化水素基と、酸素原子、硫黄原子、カルボニル基及びアミノ基から選択された少なくとも1種の連結基とからなる2価の基を示す。pは0以上の整数を示し、nは0又は1を示し、mは1〜5の整数を示し、mが1の場合、環Zは、5−オキサビシクロ[1.1.1]ペンタン環、6−オキサビシクロ[2.1.1]ヘキサン環、7−オキサビシクロ[2.2.1]ヘプタン環(7−オキサノルボルナン環)、7−オキサビシクロ[3.1.1]ヘプタン環、8−オキサビシクロ[3.2.1]オクタン環、8−オキサビシクロ[4.1.1]オクタン環、9−オキサビシクロ[3.3.1]ノナン環、及び9−オキサビシクロ[4.2.1]ノナン環から選択される環である。s及びtは、それぞれ、0〜7の整数を示し、sとtの合計は1〜6の整数である。p、n、mが2以上の場合、括弧内の置換基は同一であってもよく、異なっていてもよい]
で表される酸素原子含有多環式化合物を提供する。
である。
で表される基が含まれる。
で表されるビニルエステル化合物が挙げられる。
出発原料としてのフラン(100g、1.48mol)とアクリル酸メチル(129g、1.50mol)、及び塩化アルミニウム(19.4g、0.145mol)を、ジクロロメタン溶媒(300ml)に加え、室温でDiels-Alder反応を行った。反応液を希塩化水素水溶液でクエンチ後、水洗、アルカリ洗浄、濃縮を行ったところ、7−オキサビシクロ[2.2.1]−2−ヘプテン−6−カルボン酸メチルをほぼ定量的に得た。この7−オキサビシクロ[2.2.1]−2−ヘプテン−6−カルボン酸メチル(100g、0.65mol)、及びLiAlH4(25g、0.65mol)を、テトラヒドロフラン(THF)溶媒に添加し、氷浴下で還元反応を行った。次いで、氷浴下、メタノールでクエンチ後、THFで希釈し、濾過して得た濾液を濃縮したところ、6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]−2−ヘプテンを得た。
[2−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと3−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンの混合物のスペクトルデータ]
1H−NMR(CDCl3、TMS)500MHz δ:0.78−1.13(m,2H),1.44−1.78(m,2H),1.78−1.90(m,2H)、2.23−2.26(m,1H),3.26−3.37(m,2H),3.62−3.89(m,2H),4.23−4.44(m,1H)
実施例1で得た混合物のうち、2−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンを以下のビニル化工程に付した。すなわち、前記ジヒドロキシ化合物に対して、プロピオン酸ビニル4当量、ジ−μ−クロロビス(1,5−シクロオクタジエン)二イリジウム(I)[Ir(cod)Cl]20.7モル%、及び炭酸ナトリウム1.5当量のトルエン混合液を4.5重量倍加え、105℃で2時間反応を行った。GC−MSにより分析したところ、2−ヒドロキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンが収率67%で生成していた。反応液を減圧蒸留して上記の化合物を得た。
[2−ヒドロキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンのスペクトルデータ]
1H−NMR(CDCl3、TMS)500MHz δ:1.31−2.21(m,5H),3.42(m,1H),3.92−4.12(m,5H),5.13−5.27(m,1H),6.24−6.29(dd,1H)
実施例1で得た2−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと3−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンの混合物を以下のビニル化工程に付した。すなわち、前記ジヒドロキシ化合物の混合物に対して、プロピオン酸ビニル4当量、ジ−μ−クロロビス(1,5−シクロオクタジエン)二イリジウム(I)[Ir(cod)Cl]22モル%、及び炭酸ナトリウム1.5当量のトルエン混合液を4.5重量倍加え、105℃で5時間反応を行った。GC−MSにより分析したところ、下記式(5)で表される2−ビニルオキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと下記式(6)で表される3−ビニルオキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンとの混合物が収率84%で生成していた。反応液を減圧蒸留して上記の化合物を得た。
1H−NMR(CDCl3、TMS)500MHz δ:0.94−2.59(m,5H),3.42−3.56(m,2H),3.99−4.24(m,5H),4.56−4.65(m,2H),6.34−6.47(m,2H)
6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]−2−ヘプテン(50g、0.40mol)に、ジクロロメタン溶媒(850ml)を加えて撹拌し、純度60%のm−クロロ過安息香酸(mCPBA:276.8g、0.96mol)をゆっくり添加した。撹拌しながら室温で約2時間熟成させた後、5重量%チオ硫酸ナトリウム水溶液を用いて過酸化物が消失するまで洗浄した。水層を除去し、回収した有機層を5重量%炭酸水素ナトリウム水溶液及び飽和塩化ナトリウム水溶液で順次洗浄し、有機層を濃縮することにより粗エポキシ体を得た。この粗エポキシ体を、100重量倍のメタノールに溶解し、2重量%の濃硫酸を添加して室温で約2時間撹拌し、メタノールを除去した。GC−MSにより分析したところ、2−ヒドロキシ−3−メトキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと2−メトキシ−3−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンの混合物が収率92%で生成していた。反応液を減圧蒸留して上記の化合物を得た。
[2−ヒドロキシ−3−メトキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと2−メトキシ−3−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンとの混合物のスペクトルデータ]
1H−NMR(CDCl3、TMS)500MHz δ:1.23−2.14(m,5H),3.20−3.49(m,6H),4.24−4.46(m,1H),5.11−5.14(m,1H),5.78−5.86(m,1H)
実施例4で得た2−ヒドロキシ−3−メトキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと2−メトキシ−3−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンとの混合物を、実施例2と同様のビニル化工程に付した。この反応液をGC−MSにより分析したところ、2−ヒドロキシ−3−メトキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと2−メトキシ−3−ヒドロキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンの混合物が収率68%で生成していた。反応液を減圧蒸留して上記の化合物を得た。
[2−ヒドロキシ−3−メトキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと2−メトキシ−3−ヒドロキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンとの混合物のスペクトルデータ]
1H−NMR(CDCl3、TMS)500MHz δ:1.19−2.14(m,4H),3.20−3.24(m,4H),3.92−4.56(m,5H),5.02−5.14(m,1H),5.78−5.86(m,1H),6.43(dd,1H)
実施例4で得た2−ヒドロキシ−3−メトキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと2−メトキシ−3−ヒドロキシ−6−ヒドロキシメチル−7−オキサビシクロ[2.2.1]ヘプタンとの混合物を、実施例3と同様のビニル化工程に付した。この反応液をGC−MSにより分析したところ、下記式(7)で表される2−ビニルオキシ−3−メトキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンと下記式(8)で表される2−メトキシ−3−ビニルオキシ−6−ビニルオキシメチル−7−オキサビシクロ[2.2.1]ヘプタンの混合物が収率74%で生成していた。この反応液を減圧蒸留して上記の化合物を得た。
1H−NMR(CDCl3、TMS)500MHz δ:1.23−1.78(m,3H),3.24−3.48(m,4H),3.92−4.49(m,7H),5.21−5.24(m,1H),6.13−6.21(m,1H),6.34−6.48(m,2H)
ギ酸(188ml、5mol)と1,5−シクロオクタジエン(1.2L、10mol)を反応容器に入れ、撹拌しながら氷浴中で30重量%過酸化水素水(2.6L、23mol)を滴下した。滴下終了後、液温を50℃に保ち、系が均一となるまで約8時間撹拌を続けた。この反応液をGC−MSにより分析したところ、2,6−ジヒドロキシ−9−オキサビシクロ[3.3.1]ノナンと2,5−ジヒドロキシ−9−オキサビシクロ[4.2.1]ノナンの混合物が収率90%で生成していた。この反応液が濁るまで水を加え、次いで、氷浴により冷却し、析出した固体を濾別したところ、純度95%の上記混合物からなる高純度品を得ることができた。
[2,6−ジヒドロキシ−9−オキサビシクロ[3.3.1]ノナンと2,5−ジヒドロキシ−9−オキサビシクロ[4.2.1]ノナンとの混合物のスペクトルデータ]
1H−NMR(CDCl3、TMS)500MHz δ:1.79−2.16(m,10H),3.22−3.46(m,2H),3.67−3.72(m,2H)
実施例7で得た2,6−ジヒドロキシ−9−オキサビシクロ[3.3.1]ノナンと2,5−ジヒドロキシ−9−オキサビシクロ[4.2.1]ノナンとの混合物を、実施例2と同様のビニル化工程に付した。反応液を、GC−MSにより分析したところ、2−ヒドロキシ−6−ビニルオキシ−9−オキサビシクロ[3.3.1]ノナンと2−ヒドロキシ−5−ビニルオキシ−9−オキサビシクロ[4.2.1]ノナンの混合物が収率66%で生成していた。
[2−ヒドロキシ−6−ビニルオキシ−9−オキサビシクロ[3.3.1]ノナンと2−ヒドロキシ−5−ビニルオキシ−9−オキサビシクロ[4.2.1]ノナンの混合物のスペクトルデータ]
1H−NMR(CDCl3、TMS)500MHz δ:1.56−1.93(m,8H),2.2(br,1H),3.32−3.89(m,4H),3.67−3.72(m,2H)
実施例7で得た2,6−ジヒドロキシ−9−オキサビシクロ[3.3.1]ノナンと2,5−ジヒドロキシ−9−オキサビシクロ[4.2.1]ノナンとの混合物を、実施例3と同様のビニル化工程に付した。反応液を、GC−MSにより分析したところ、下記式(9)で表される2,6−ビス(ビニルオキシ)−9−オキサビシクロ[3.3.1]ノナンと下記式(10)で表される2,5−(ビニルオキシ)−9−オキサビシクロ[4.2.1]ノナンの混合物が収率78%で生成していた。
1H−NMR(CDCl3、TMS)500MHz δ:1.78−2.32(m,8H),3.96−4.64(m,8H),6.32−6.47(m,2H)
実施例3、6、9で得た酸素原子含有多環式ビニルエーテル化合物及び比較例1の環式基含有ビニルエーテル化合物に対して、それぞれ、光重合開始剤(トリアリルスルホニウムヘキサフルオロホスフェイトのプロピレンカーボネート溶液:商品名「UVACURE」、ダイセル化学工業(株)製)を3重量%混合して重合性組成物を得た。
得られた重合性組成物を石英ガラス上に約200μmの厚みに塗布し、焦点距離15cmでUVランプ(波長の構成:365nm、405nm、436nm、強度:250W)を照射し、表面に粘りがなくなるまでの照射時間を測定した。形成された硬化物について、JIS K5400に準拠した試験により鉛筆硬度を測定した。これらの結果を表1に示す。
Claims (3)
- 下記式(1)
で表される基を示し、少なくとも1つは上記式(2)で表される基である。Wは(i)ヒドロキシル基、ヒドロキシメチル基、アミノ基、カルボキシル基、スルホ基、ハロゲン原子、オキソ基、シアノ基、ニトロ基、複素環式基、炭化水素基、及びハロアルキル基から選択される基で水素原子が置換されていてもよい2価の炭化水素基、(ii)ヒドロキシル基、ヒドロキシメチル基、アミノ基、カルボキシル基、スルホ基、ハロゲン原子、オキソ基、シアノ基、ニトロ基、複素環式基、炭化水素基、及びハロアルキル基から選択される基で水素原子が置換されていてもよい2価の炭化水素基と、酸素原子、硫黄原子、カルボニル基及びアミノ基から選択された少なくとも1種の連結基とからなる2価の基を示す。pは0以上の整数を示し、nは0又は1を示し、mは1〜5の整数を示し、mが1の場合、環Zは、5−オキサビシクロ[1.1.1]ペンタン環、6−オキサビシクロ[2.1.1]ヘキサン環、7−オキサビシクロ[2.2.1]ヘプタン環(7−オキサノルボルナン環)、7−オキサビシクロ[3.1.1]ヘプタン環、8−オキサビシクロ[3.2.1]オクタン環、8−オキサビシクロ[4.1.1]オクタン環、9−オキサビシクロ[3.3.1]ノナン環、及び9−オキサビシクロ[4.2.1]ノナン環から選択される環である。s及びtは、それぞれ、0〜7の整数を示し、sとtの合計は1〜6の整数である。p、mが2以上の場合、括弧内の置換基は同一であってもよく、異なっていてもよい]
で表される酸素原子含有多環式化合物。 - 重合開始剤、及び請求項1記載の酸素原子含有多環式化合物を含む重合性組成物(インクを除く)。
- 請求項2記載の重合性組成物を硬化して得られる硬化物。
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