JP2019112322A - 歯科材料に好適な重合性単量体及びそれを用いた歯科用組成物 - Google Patents
歯科材料に好適な重合性単量体及びそれを用いた歯科用組成物 Download PDFInfo
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- JP2019112322A JP2019112322A JP2017244923A JP2017244923A JP2019112322A JP 2019112322 A JP2019112322 A JP 2019112322A JP 2017244923 A JP2017244923 A JP 2017244923A JP 2017244923 A JP2017244923 A JP 2017244923A JP 2019112322 A JP2019112322 A JP 2019112322A
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- polymerizable monomer
- meth
- dental
- bis
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- 239000000203 mixture Substances 0.000 title claims description 71
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- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- -1 acryloxy group Chemical group 0.000 claims description 116
- 125000004432 carbon atom Chemical group C* 0.000 claims description 30
- 125000001424 substituent group Chemical group 0.000 claims description 27
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- 239000003505 polymerization initiator Substances 0.000 claims description 20
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 6
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
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- TZKUEMHGRFBQIX-UHFFFAOYSA-N cyclohexylmethylsilane Chemical compound [SiH3]CC1CCCCC1 TZKUEMHGRFBQIX-UHFFFAOYSA-N 0.000 description 4
- IESPKCNRKMAVIB-UHFFFAOYSA-N dichloro(dicyclohexyl)silane Chemical compound C1CCCCC1[Si](Cl)(Cl)C1CCCCC1 IESPKCNRKMAVIB-UHFFFAOYSA-N 0.000 description 4
- MCPOBKGRILHVPP-UHFFFAOYSA-N dicyclopentylsilane Chemical compound C1CCCC1[SiH2]C1CCCC1 MCPOBKGRILHVPP-UHFFFAOYSA-N 0.000 description 4
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- JTGAUXSVQKWNHO-UHFFFAOYSA-N ditert-butylsilicon Chemical compound CC(C)(C)[Si]C(C)(C)C JTGAUXSVQKWNHO-UHFFFAOYSA-N 0.000 description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
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- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 3
- UEKHZPDUBLCUHN-UHFFFAOYSA-N 2-[[3,5,5-trimethyl-6-[2-(2-methylprop-2-enoyloxy)ethoxycarbonylamino]hexyl]carbamoyloxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOC(=O)NCCC(C)CC(C)(C)CNC(=O)OCCOC(=O)C(C)=C UEKHZPDUBLCUHN-UHFFFAOYSA-N 0.000 description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 3
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- 239000011591 potassium Substances 0.000 description 1
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- DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 description 1
- 229940099427 potassium bisulfite Drugs 0.000 description 1
- 235000010259 potassium hydrogen sulphite Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- HPWMVNFJSFHJIW-UHFFFAOYSA-M potassium;2,4,6-tri(propan-2-yl)benzenesulfinate Chemical compound [K+].CC(C)C1=CC(C(C)C)=C(S([O-])=O)C(C(C)C)=C1 HPWMVNFJSFHJIW-UHFFFAOYSA-M 0.000 description 1
- NLZLDWFYQXFPSZ-UHFFFAOYSA-M potassium;2,4,6-triethylbenzenesulfinate Chemical compound [K+].CCC1=CC(CC)=C(S([O-])=O)C(CC)=C1 NLZLDWFYQXFPSZ-UHFFFAOYSA-M 0.000 description 1
- YVHWGMMGEAQQRT-UHFFFAOYSA-M potassium;4-methylbenzenesulfinate Chemical compound [K+].CC1=CC=C(S([O-])=O)C=C1 YVHWGMMGEAQQRT-UHFFFAOYSA-M 0.000 description 1
- LZSBNSVOXWMXLL-UHFFFAOYSA-M potassium;benzenesulfinate Chemical compound [K+].[O-]S(=O)C1=CC=CC=C1 LZSBNSVOXWMXLL-UHFFFAOYSA-M 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- SLUHLANJIVXTRQ-UHFFFAOYSA-N pyridin-2-ylthiourea Chemical compound NC(=S)NC1=CC=CC=N1 SLUHLANJIVXTRQ-UHFFFAOYSA-N 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 239000003829 resin cement Substances 0.000 description 1
- 150000003284 rhodium compounds Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000012419 sodium bis(2-methoxyethoxy)aluminum hydride Substances 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- CMZUMMUJMWNLFH-UHFFFAOYSA-N sodium metavanadate Chemical compound [Na+].[O-][V](=O)=O CMZUMMUJMWNLFH-UHFFFAOYSA-N 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- VMMZJFAHOAKUQM-UHFFFAOYSA-N sodium;1,3,5-trimethyl-1,3-diazinane-2,4,6-trione Chemical compound [Na].CC1C(=O)N(C)C(=O)N(C)C1=O VMMZJFAHOAKUQM-UHFFFAOYSA-N 0.000 description 1
- GRBCNEIBDFNEES-UHFFFAOYSA-M sodium;2,4,6-trimethylbenzenesulfinate Chemical compound [Na+].CC1=CC(C)=C(S([O-])=O)C(C)=C1 GRBCNEIBDFNEES-UHFFFAOYSA-M 0.000 description 1
- CHLCPTJLUJHDBO-UHFFFAOYSA-M sodium;benzenesulfinate Chemical compound [Na+].[O-]S(=O)C1=CC=CC=C1 CHLCPTJLUJHDBO-UHFFFAOYSA-M 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000004079 stearyl 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])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])[H] 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- JIYXDFNAPHIAFH-UHFFFAOYSA-N tert-butyl 3-tert-butylperoxycarbonylbenzoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC(C(=O)OC(C)(C)C)=C1 JIYXDFNAPHIAFH-UHFFFAOYSA-N 0.000 description 1
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 150000003510 tertiary aliphatic 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
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- ZEMGGZBWXRYJHK-UHFFFAOYSA-N thiouracil Chemical class O=C1C=CNC(=S)N1 ZEMGGZBWXRYJHK-UHFFFAOYSA-N 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000009849 vacuum degassing Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- UUUGYDOQQLOJQA-UHFFFAOYSA-L vanadyl sulfate Chemical compound [V+2]=O.[O-]S([O-])(=O)=O UUUGYDOQQLOJQA-UHFFFAOYSA-L 0.000 description 1
- 229940041260 vanadyl sulfate Drugs 0.000 description 1
- 229910000352 vanadyl sulfate Inorganic materials 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- XASAPYQVQBKMIN-UHFFFAOYSA-K ytterbium(iii) fluoride Chemical compound F[Yb](F)F XASAPYQVQBKMIN-UHFFFAOYSA-K 0.000 description 1
- 229940105963 yttrium fluoride Drugs 0.000 description 1
- RBORBHYCVONNJH-UHFFFAOYSA-K yttrium(iii) fluoride Chemical compound F[Y](F)F RBORBHYCVONNJH-UHFFFAOYSA-K 0.000 description 1
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Abstract
Description
すなわち、本発明は、
[1]下記一般式(1)
で表される重合性単量体;
[2]25℃における粘度が1000cP以下である、前記[1]に記載の重合性単量体;
[3]R1及びR2がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の1価の脂肪族炭化水素基、又は置換基を有していてもよい炭素数6〜20の1価の芳香族炭化水素基(但しR1及びR2はいずれもケイ素原子を含まない)である、前記[1]又は[2]に記載の重合性単量体;
[4]R1及び/又はR2が置換基を有していてもよいフェニル基である、前記[1]〜[3]のいずれかに記載の重合性単量体;
[5]R1及びR2の少なくとも1つは置換基を有さないフェニル基である、前記[4]に記載の重合性単量体;
[6]R1及びR2がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の脂肪族炭化水素基(但しR1及びR2はいずれもケイ素原子を含まない)である、前記[1]〜[3]のいずれかに記載の重合性単量体;
[7]R3及びR4がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の2価の脂肪族炭化水素基、又は置換基を有していてもよい炭素数6〜20の2価の芳香族炭化水素基(但しR3及びR4はいずれもケイ素原子を含まない)である、前記[1]〜[6]のいずれかに記載の重合性単量体;
[8]R3及びR4がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の2価の脂肪族炭化水素基(但しR3及びR4はいずれもケイ素原子を含まない)である、前記[1]〜[7]のいずれかに記載の重合性単量体;
[9]R3及びR4の少なくとも1つは置換基を有さない脂肪族炭化水素基である、前記[7]又は[8]に記載の重合性単量体;
[10]前記[1]〜[9]のいずれかに記載の重合性単量体を含む歯科用組成物;
[11]さらに、重合開始剤及びフィラーを含む、前記[10]に記載の歯科用組成物;
[12]前記[10]又は[11]のいずれかに記載の歯科用組成物からなる歯科用コンポジットレジン;
に関する。
一官能性単量体としては、例えば、メチル(メタ)アクリレート、イソブチル(メタ)アクリレート、ベンジル(メタ)アクリレート、ラウリル(メタ)アクリレート、2−(N,N−ジメチルアミノ)エチル(メタ)アクリレート、2,3−ジブロモプロピル(メタ)アクリレート、3−メタクリロイルオキシプロピルトリメトキシシラン、11−メタクリロイルオキシウンデシルトリメトキシシラン、2−ヒドロキシエチル(メタ)アクリレート、3−ヒドロキシプロピル(メタ)アクリレート、4−ヒドロキシブチル(メタ)アクリレート、6−ヒドロキシヘキシル(メタ)アクリレート、10−ヒドロキシデシル(メタ)アクリレート、プロピレングリコールモノ(メタ)アクリレート、グリセリンモノ(メタ)アクリレート、エリトリトールモノ(メタ)アクリレート、イソボルニル(メタ)アクリレート、3−フェノキシベンジル(メタ)アクリレートなどの(メタ)アクリレート系重合性単量体;N−メチロール(メタ)アクリルアミド、N−ヒドロキシエチル(メタ)アクリルアミド、N、N−(ジヒドロキシエチル)(メタ)アクリルアミド、N,N−ジメチル(メタ)アクリルアミド、N,N−ジエチル(メタ)アクリルアミド、N,N−ジ−n−プロピル(メタ)アクリルアミド、N−エチル−N−メチル(メタ)アクリルアミドなどの(メタ)アクリルアミド系重合性単量体;(メタ)アクリロイルモルホリン、(メタ)アクリロイルオキシドデシルピリジニウムブロマイド、(メタ)アクリロイルオキシドデシルピリジニウムクロライド、(メタ)アクリロイルオキシドデシルピリジニウムブロマイド、(メタ)アクリロイルオキシヘキサデシルピリジニウムクロライドなどが挙げられる。
二官能性単量体としては、芳香族化合物系の二官能性重合性単量体、脂肪族化合物系の二官能性重合性単量体が挙げられる。
三官能性以上の単量体としては、例えば、トリメチロールプロパントリ(メタ)アクリレート、トリメチロールエタントリ(メタ)アクリレート、トリメチロールメタントリ(メタ)アクリレート、ペンタエリスリトールトリ(メタ)アクリレート、ペンタエリスリトールテトラ(メタ)アクリレート、ジペンタエリスリトールトリ(メタ)アクリレート、ジペンタエリスリトールテトラ(メタ)アクリレート、ジペンタエリスリトールペンタ(メタ)アクリレート、N,N−(2,2,4−トリメチルヘキサメチレン)ビス〔2−(アミノカルボキシ)プロパン−1,3−ジオール〕テトラメタクリレート、1,7−ジアクリロイルオキシ−2,2,6,6−テトラアクリロイルオキシメチル−4−オキサヘプタンなどが挙げられる。
1H−NMRスペクトルは日本電子株式会社製JNM−GSX270スペクトロメーター又はBruker社製 ULTRA SHIELD 400 PLUSを用い、それぞれ270MHz及び400MHzで測定した。溶媒には重水素化クロロホルムを用い、内部標準としてテトラメチルシラン(TMS)を加えた。
装置:ACQUITY UPLC(日本ウォーターズ株式会社製)
カラム:ACQUITY UPLC BEH C18 1.7μm(日本ウォーターズ株式会社製)
移動相:メタノール/水=45/55
流量:0.5mL/min
検出器:RI,UV
カラム温度:50℃
注入量:1.0μL
装置:GC−2014(株式会社島津製作所製)
カラム:DB−1ms(アジレント・テクノロジー社製)
キャリアガス:窒素
検出器:FID
検出器温度:300℃
カラム温度:50℃で5分間保持後、20℃/分の昇温速度で250℃まで昇温し、次いで10℃/分の昇温速度で300℃まで昇温し、300℃で10分間保持
注入量:0.2μL
粘度計(東機産業株式会社製、TV−30E型粘度計、JIS K−7117−2:1999に準拠、コーン・プレートタイプ)を用いて、0.8°×R24のコーンロータで、サンプル量0.6mL、25℃にて測定した。1分間のプレヒートを行った後、測定を開始し、5分後の測定値をその粘度とした。
各実施例及び比較例で得られた歯科用組成物を真空脱泡後、ステンレス製の金型(寸法2mm×2mm×25mm)に充填し、上下をスライドガラスで圧接し、歯科用LED光照射器(株式会社モリタ製、商品名「ペンキュアー2000」)で1点10秒、片面を5点ずつ、スライドガラスの両面に光を照射して硬化させて硬化物の試験片を得た。各実施例及び比較例について、硬化物を5本ずつ作製し、硬化物は、金型から取り出した後、37℃の蒸留水中に24時間保管した。各試験片について、JIS T6514:2015及びISO4049:2009に準拠して、精密万能試験機(株式会社島津製作所製、商品名「AGI−100」)を用いて、支点間距離20mm、クロスヘッドスピード1mm/分の条件下で曲げ強さを3点曲げ試験で測定した。各試験片の測定値の平均値を算出し、曲げ強さとした。曲げ強さは100MPa以上が好ましく、110MPa以上がより好ましく、120MPa以上が最も好ましい。
各実施例及び比較例で得られた歯科用組成物のペースト0.5ccを測りとり、その上にガラス板を介して1kgの荷重を30秒間かけ、ペーストを押しつぶした。展延された円板状のペーストの最大直径及び最小直径の2点を測定し、2点の平均値(mm)を稠度とした。稠度が大きいほどペーストが柔らかいことを示し、ペーストの操作性の観点から10mm以上が好ましく、12mm以上がより好ましく、14mm以上がさらに好ましい。
厚さ4.0mmのガラス板上に設置したリング状の金型(ステンレス製、内径5.5mm×厚さ0.8mm)内に、各実施例及び比較例で作製したペースト(歯科用組成物)を充填した。前記ガラス板は、粒径50μmのアルミナパウダーでサンドブラスト処理したものを使用した。充填したペースト上に、万能試験機(オートグラフAG−100kNI、株式会社島津製作所製)と連結したステンレス製治具(φ5mm)を設置した。次いで、歯科用LED光照射器(株式会社モリタ製、商品名「ペンキュアー2000」)を用いて、ガラス板越しに20秒間ペーストに光照射してペーストを硬化させた。この際、かかる光照射によって進行する歯科用組成物の重合(硬化)に伴う重合収縮応力を、上記万能試験機で測定した。重合収縮応力が小さいほど収縮による剥離のリスクを小さくすることができることに加えて、一度により多くの硬化性組成物を充填することができるようになり、操作性が向上する。重合収縮応力は、12MPa以下であることが好ましく、10MPa未満であることがより好ましい。
歯科用エアータービンを用いて、直径約4mm、深さ約3mmの窩洞を、牛歯抜去歯に形成し、当該窩洞の内面に光重合型歯科用ボンディング材(クラレノリタケデンタル株式会社製、商品名「クリアフィル(登録商標) ユニバーサルボンド クイック」)を塗布した後、歯科用LED光照射器(株式会社モリタ製、商品名「ペンキュアー2000」)にて10秒間光照射して光重合型歯科用ボンディング材を硬化させた。次いで、各実施例、比較例で得られた歯科用組成物のペーストを窩洞内に充填した後、上記の歯科用光照射器にて20秒間光照射して、充填した歯科用組成物を硬化させた。次いで、歯根尖及び歯冠裂溝部などからの色素の浸入を防止するために、光重合型歯科用ボンディング材(クラレノリタケデンタル株式会社製、商品名「クリアフィル(登録商標) メガボンド(登録商標)」)を、窩洞修復部及びその周辺部以外の部分に塗布し、上記の歯科用光照射器にて30秒間光照射して硬化させて、試験片とした。試験片は5個作製した。次いで、試験片を、サンプル容器内の蒸留水に浸漬した状態で、37℃に設定した恒温器内に24時間放置した。試験片を取り出し、4℃の冷水(蒸留水)と60℃の温水(蒸留水)に交互に各1分間浸漬する熱サイクルを2500回行った後に、37℃の0.2%塩基性フクシン水溶液に24時間浸漬し、水洗し、歯科用エアーシリンジにて乾燥した。乾燥後、試験片を、低速ダイヤモンドカッターにて修復部分を縦方向に切断して3分割し、1個の試験片から3つの切片、すなわち5個の試験片から15個の切片を作製した。次いで、これら15個の切片について、エナメル質の窩縁及び象牙質の窩縁への色素の侵入を光学顕微鏡にて観察して、それぞれの部位について、下記の基準によりスコアを求め、15個の切片についてのスコアの平均値を算出した。この平均値は、歯科用組成物に熱履歴が加わった際に歯科用組成物と歯質の間で剥離する懸念が低減する点から、1.5以下が好ましく、1.0以下がより好ましい。
スコア0:窩壁部及び窩底部のいずれにも色素の侵入が全く認められない。
スコア1:窩底部には色素の侵入は認められないが、窩壁部には窩壁の1/2未満の色素の侵入が認められる。
スコア2:窩底部には色素の侵入は認められないが、窩壁部には窩壁の1/2以上の色素の侵入が認められる。
スコア3:窩壁部及び窩底部の両方に色素の侵入が認められる。
(ジフェニルビス[3−(メタクリロキシ)プロピル]シラン(以下、DPPSと表記)の合成)
100mLナスフラスコにアリルメタクリレート(東京化成工業株式会社製,12.6g,100mmol)を秤量し、p−メトキシフェノール(和光純薬工業株式会社製,100mg)を加え撹拌した。系内に触媒である白金−ジビニルテトラメチルジシロキサン錯体(ゲレスト社製)をスポイトで2滴加え、ジフェニルシラン(ゲレスト社製,7.37g,40mmol)を投入した。その後室温で撹拌しながら7日間反応させた。7日間反応後、反応溶液の一部をサンプリングして1H−NMR測定を行い、反応の進行を確認した。その結果、原料由来のH−Si−Hのピークの消失が確認できたため、反応を終了させた。得られた黄色の液体を、シリカゲルカラムクロマトグラフィーを用いて精製し(溶媒:n−へキサン/酢酸エチル=30/1(体積比))、溶媒をロータリーエバポレーターを用いて減圧留去することで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるDPPS)であることを確認した。得られた重合性単量体の粘度は320cPであった。
(メチルフェニルビス[3−(メタクリロキシ)プロピル]シラン(以下、MPPSと表記)の合成)
実施例1において、ジフェニルシランの替わりにメチルフェニルシラン(ゲレスト社製,4.88g,40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるMPPS)であることを確認した。得られた重合性単量体の粘度は36cPであった。
(メチルフェニルビス[3−(メタクリロキシ)ウンデシル]シラン(以下、MPUSと表記)の合成)
実施例1において、アリルメタクリレートを、特開昭63−211252号の実施例1に記載の方法で合成した10−ウンデセニルメタクリレートに変更し、ジフェニルシランを、メチルフェニルシラン(2.45g,20mmol)及び10−ウンデセニルメタクリレート(10.72g,45mmol)に変更して反応を行った以外は、実施例1と同様にして反応を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるMPUS)であることを確認した。得られた重合性単量体の粘度は71cPであった。
(ジシクロヘキシルシランの合成)
温度計、コンデンサー、滴下ロート及び撹拌装置を備えた300mL二つ口フラスコに、ジシクロヘキシルジクロロシラン(ゲレスト社製)9.55g(0.036mol)とトルエン90mLとを入れた。フラスコ内の溶液を0℃以下に保持しながら撹拌し、滴下ロートより水素化ビス(2−メトキシエトキシ)アルミニウムナトリウムのトルエン溶液(濃度約3.6mol/L)21mLをゆっくりと滴下した。滴下終了後、徐々に室温へと昇温して4時間撹拌して還元反応を行った。この間、原料及び生成物は反応液に溶解しており、反応系は均一であった。その後、反応混合物を加水分解した後、シクロペンチルメチルエーテルで抽出し、抽出液を減圧下で濃縮して、無色液体を得た。得られた無色液体について、ガスクロマトグラフィー(GC)、1H−NMRにより分析したところ、ジシクロヘキシルシランの生成が確認できた。また1H−NMR測定時に内部標準物質を添加し反応収率を算出したところ、ジシクロヘキシルシランの収率は75%であった。
(ジシクロヘキシルビス[3−(メタクリロキシ)プロピル]シラン(以下、DCyhPSと表記)の合成)
実施例1において、ジフェニルシランの替わりに合成例1で得られたジシクロヘキシルシラン(7.78g、40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるDCyhPS)であることを確認した。得られた重合性単量体の粘度は270cPであった。
(シクロヘキシルメチルシランの合成)
合成例1において、ジシクロヘキシルジクロロシランの替わりにシクロヘキシルメチルジクロロシラン(ゲレスト社製、7.1g、0.036mmol)を用いた以外は、合成例1と同様にして合成を行った。得られた無色液体について、ガスクロマトグラフィー(GC)、1H−NMRにより分析したところ、シクロヘキシルメチルシランの生成が確認できた。また1H−NMR測定時に内部標準物質を添加し反応収率を算出したところ、シクロヘキシルメチルシランの収率は86%であった。
(シクロヘキシルメチルビス[3−(メタクリロキシ)プロピル]シラン(以下、CyhMPSと表記)の合成)
実施例1において、ジフェニルシランの替わりに合成例2で得られたシクロヘキシルメチルシラン(5.13g、40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるCyhMPS)であることを確認した。得られた重合性単量体の粘度は9cPであった。
(ジシクロペンチルシランの合成)
合成例1において、ジシクロヘキシルジクロロシランの替わりにジシクロペンチルジクロロシラン(ゲレスト社製、8.54g、0.036mmol)を用いた以外は、合成例1と同様にして合成を行った。得られた無色液体について、ガスクロマトグラフィー(GC)、1H−NMRにより分析したところ、ジシクロペンチルシランの生成が確認できた。また1H−NMR測定時に内部標準物質を添加し反応収率を算出したところ、ジシクロペンチルシランの収率は71%であった。
(ジシクロペンチルビス[3−(メタクリロキシ)プロピル]シラン(以下、DCypPSと表記)の合成)
実施例1において、ジフェニルシランの替わりに合成例3で得られたジシクロペンチルシラン(6.73g、40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるDCypPS)であることを確認した。得られた重合性単量体の粘度は90cPであった。
(ジ−tert−ブチルシランの合成)
合成例1において、ジシクロヘキシルジクロロシランの替わりにジ−t−ブチルジクロロシラン(ゲレスト社製、7.68g、0.036mmol)を用いた以外は、合成例1と同様にして合成を行った。得られた無色液体について、ガスクロマトグラフィー(GC)、1H−NMRにより分析したところ、ジ−tert−ブチルシランの生成が確認できた。また1H−NMR測定時に内部標準物質を添加し反応収率を算出したところ、ジ−tert−ブチルシランの収率は71%であった。
(ジ−tert−ブチルビス[3−(メタクリロキシ)プロピル]シラン(以下、DtBPSと表記)の合成)
実施例1において、ジフェニルシランの替わりに合成例4で得られたジ−tert−ブチルシラン(5.77g、40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるDtBPS)であることを確認した。得られた重合性単量体の粘度は4cPであった。
(1−アダマンチルメチルビス[3−(メタクリロキシ)プロピル]シラン(以下、AMPSと表記)の合成)
実施例1において、ジフェニルシランの替わりに1−アダマンチルメチルシラン(Capot Chemical社製,7.21g,40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるAMPS)であることを確認した。得られた重合性単量体の粘度は550cPであった。
(ジモルホリノ−[3−(メタクリロキシ)プロピル]シラン(以下、DMoPSと表記)の合成)
実施例1において、ジフェニルシランの替わりにビスモルホリノシラン(ゲレスト社製,8.09g,40mmol)を用いた以外は、実施例1と同様にして合成を行った。精製を行うことで、無色透明の液体が得られた。1H−NMR測定及びUPLC分析から、得られた無色透明の液体が目的とする重合性単量体(下記式で表されるDMoPS)であることを確認した。得られた重合性単量体の粘度は870cPであった。
実施例1〜9の重合性単量体、及び下記に示す原料を、表1に記載の質量比にて常温(23℃)暗所で混合して、各ペースト(歯科用組成物)を調製した。これらのペーストについて、上記した方法で各特性を調べた。
3G:トリエチレングリコールジメタクリレート
DD:1,10−デカンジオールジメタクリレート
D2.6E:2,2−ビス〔4−メタクリロイルオキシポリエトキシフェニル〕プロパン(エトキシ基の平均付加モル数:2.6)
UDMA:2,2,4−トリメチルヘキサメチレンビス(2−カルバモイルオキシエチル)ジメタクリレート
Bis−GMA:2,2−ビス[4−〔3−メタクリロイルオキシ−2−ヒドロキシプロポキシ〕フェニル]プロパン
CQ:カンファーキノン
TMDPO:2,4,6−トリメチルベンゾイルジフェニルホスフィンオキシド
PDE:4−(N,N−ジメチルアミノ)安息香酸エチル
BHT:3,5−ジ−t−ブチル−4−ヒドロキシトルエン
UF1.0:3−メタクリロイルオキシプロピルトリメトキシシラン表面処理バリウムガラス粉、ショット社製「GM27884 UF1.0」、平均粒子径1.0μm
NF180:3−メタクリロイルオキシプロピルトリメトキシシラン表面処理バリウムガラス粉、ショット社製「GM27884 NF180」、平均粒子径0.18μm
P−500:後述の製造例1により作製した。
有機無機複合フィラー(CF)は、後述の製造例2により作製した。
凝集シリカ「シリカマイクロビード P−500(一次粒子の平均粒子径12nm、凝集体の平均粒子径2μm)」(日揮触媒化成株式会社製)100g、3−メタクリロキシプロピルトリメトキシシラン20g、及びトルエン200mLを三口フラスコに入れ、2時間、室温下で撹拌した。トルエンを減圧下で留去した後、40℃で16時間真空乾燥を行い、さらに90℃で3時間加熱し、平均粒子径1.6μm、屈折率1.44、比表面積99m2/g、細孔容積0.19mL/gの無機フィラー(P−500)を得た。
予め重合開始剤としてアゾビスイソブチロニトリル(AIBN)を1質量%溶解した、Bis−GMAと3Gの重合性単量体混合物(質量比1:1)100質量部に対して、無機フィラーとしてNF180を100質量部添加、混合しペースト化した。これを100℃、減圧雰囲気下で5時間加熱重合した。得られた重合硬化物を、振動ボールミルを用いて、平均粒子径が5μmとなるまで粉砕した。得られた粉砕フィラー100gに対して、γ−メタクリロイルオキシプロピルトリメトキシシラン2質量%含有エタノール溶液200mL中、90℃で5時間還流することで表面処理を行ない、有機無機複合フィラー(CF)を得た。
Claims (12)
- 25℃における粘度が1000cP以下である、請求項1に記載の重合性単量体。
- R1及びR2がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の1価の脂肪族炭化水素基、又は置換基を有していてもよい炭素数6〜20の1価の芳香族炭化水素基(但しR1及びR2はいずれもケイ素原子を含まない)である、請求項1又は2に記載の重合性単量体。
- R1及び/又はR2が置換基を有していてもよいフェニル基である、請求項1〜3のいずれか1項に記載の重合性単量体。
- R1及びR2の少なくとも1つは置換基を有さないフェニル基である、請求項4に記載の重合性単量体。
- R1及びR2がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の脂肪族炭化水素基(但しR1及びR2はいずれもケイ素原子を含まない)である、請求項1〜3のいずれか1項に記載の重合性単量体。
- R3及びR4がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の2価の脂肪族炭化水素基、又は置換基を有していてもよい炭素数6〜20の2価の芳香族炭化水素基(但しR3及びR4はいずれもケイ素原子を含まない)である、請求項1〜6のいずれか1項に記載の重合性単量体。
- R3及びR4がそれぞれ独立に、置換基を有していてもよい炭素数1〜20の2価の脂肪族炭化水素基(但しR3及びR4はいずれもケイ素原子を含まない)である、請求項1〜7のいずれか1項に記載の重合性単量体。
- R3及びR4の少なくとも1つは置換基を有さない脂肪族炭化水素基である、請求項7又は8に記載の重合性単量体。
- 請求項1〜9のいずれか1項に記載の重合性単量体を含む歯科用組成物。
- さらに、重合開始剤及びフィラーを含む、請求項10に記載の歯科用組成物。
- 請求項10又は11に記載の歯科用組成物からなる歯科用コンポジットレジン。
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JP2019199436A (ja) * | 2018-05-16 | 2019-11-21 | 東洋インキScホールディングス株式会社 | モルホリン環含有(メタ)アクリレート化合物およびそれを用いた重合性組成物 |
WO2020111079A1 (ja) * | 2018-11-27 | 2020-06-04 | クラレノリタケデンタル株式会社 | 歯科用組成物 |
CN115417994A (zh) * | 2022-06-22 | 2022-12-02 | 鹤山波粒涂料科技有限公司 | 一种硅碳主链结构的光固化树脂及其应用 |
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