JP2011514393A5 - - Google Patents
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- Publication number
- JP2011514393A5 JP2011514393A5 JP2010544653A JP2010544653A JP2011514393A5 JP 2011514393 A5 JP2011514393 A5 JP 2011514393A5 JP 2010544653 A JP2010544653 A JP 2010544653A JP 2010544653 A JP2010544653 A JP 2010544653A JP 2011514393 A5 JP2011514393 A5 JP 2011514393A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- phenyl
- unsubstituted
- alkoxy
- 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.)
- Granted
Links
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 21
- 239000000203 mixture Substances 0.000 claims 16
- 229910052736 halogen Inorganic materials 0.000 claims 14
- 150000002367 halogens Chemical class 0.000 claims 14
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 11
- 150000001875 compounds Chemical class 0.000 claims 10
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 3
- 238000004132 cross linking Methods 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 125000001624 naphthyl group Chemical group 0.000 claims 3
- -1 o-xylylene, 2-butenylene Chemical group 0.000 claims 3
- 150000002978 peroxides Chemical class 0.000 claims 3
- 239000000853 adhesive Substances 0.000 claims 2
- 230000001070 adhesive effect Effects 0.000 claims 2
- 150000001409 amidines Chemical class 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 239000003479 dental cement Substances 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 239000000976 ink Substances 0.000 claims 2
- 239000012778 molding material Substances 0.000 claims 2
- 230000003287 optical effect Effects 0.000 claims 2
- 239000003973 paint Substances 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 238000007789 sealing Methods 0.000 claims 2
- 239000003566 sealing material Substances 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 1
- 238000003848 UV Light-Curing Methods 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000001118 alkylidene group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 238000001723 curing Methods 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000003504 photosensitizing agent Substances 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 0 CC(*)N(*)C(C)(C)N(*)C(C)(*)* Chemical compound CC(*)N(*)C(C)(C)N(*)C(C)(*)* 0.000 description 5
- HYQWHUCTTYCIAU-UHFFFAOYSA-N C(c1ccccc1)N1C(CCC2)N2CCC1 Chemical compound C(c1ccccc1)N1C(CCC2)N2CCC1 HYQWHUCTTYCIAU-UHFFFAOYSA-N 0.000 description 2
- XQZZCPHZZAZOPA-UHFFFAOYSA-N CCC(Cc1ccccc1)C(c(cc1)cc(OC)c1OC)=C(C)C Chemical compound CCC(Cc1ccccc1)C(c(cc1)cc(OC)c1OC)=C(C)C XQZZCPHZZAZOPA-UHFFFAOYSA-N 0.000 description 1
- LTXRZOZLUURSKO-UHFFFAOYSA-N COC(c1ccc(CN2C(CCC3)N3CCC2)cc1)=O Chemical compound COC(c1ccc(CN2C(CCC3)N3CCC2)cc1)=O LTXRZOZLUURSKO-UHFFFAOYSA-N 0.000 description 1
- LTXRZOZLUURSKO-HNNXBMFYSA-N COC(c1ccc(CN2[C@@H](CCC3)N3CCC2)cc1)=O Chemical compound COC(c1ccc(CN2[C@@H](CCC3)N3CCC2)cc1)=O LTXRZOZLUURSKO-HNNXBMFYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08150721.2 | 2008-01-28 | ||
| EP08150721 | 2008-01-28 | ||
| PCT/EP2009/050066 WO2009095282A2 (en) | 2008-01-28 | 2009-01-06 | Photolatent amidine bases for redox curing of radically curable formulations |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011514393A JP2011514393A (ja) | 2011-05-06 |
| JP2011514393A5 true JP2011514393A5 (https=) | 2013-03-14 |
| JP5697992B2 JP5697992B2 (ja) | 2015-04-08 |
Family
ID=39522044
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010544653A Expired - Fee Related JP5697992B2 (ja) | 2008-01-28 | 2009-01-06 | ラジカル硬化性配合物のレドックス硬化のための光潜在性アミジン塩基 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20110190412A1 (https=) |
| EP (1) | EP2238178B1 (https=) |
| JP (1) | JP5697992B2 (https=) |
| CN (1) | CN101925616A (https=) |
| WO (1) | WO2009095282A2 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5809780B2 (ja) * | 2010-04-02 | 2015-11-11 | Ｄｉｃグラフィックス株式会社 | 紫外線硬化性コーティングニス |
| WO2013039226A1 (ja) * | 2011-09-14 | 2013-03-21 | 電気化学工業株式会社 | 組成物及びそれを用いた部材の仮固定方法 |
| EP2882808B1 (de) * | 2012-08-09 | 2016-10-12 | Basf Se | Strahlungshärtbare formulierungen mit hoher haftung |
| JP5725515B2 (ja) * | 2012-11-15 | 2015-05-27 | 学校法人東京理科大学 | 光塩基発生剤及び当該光塩基発生剤を含有する感光性樹脂組成物 |
| US9650526B2 (en) * | 2014-09-09 | 2017-05-16 | 3D Systems, Inc. | Method of printing a three-dimensional article |
| WO2016057486A1 (en) * | 2014-10-06 | 2016-04-14 | Dow Global Technologies Llc | Using organic photoredox catalysts to achieve metal free photoregulated controlled radical polymerization |
| FR3030526B1 (fr) * | 2014-12-18 | 2018-06-15 | Arkema France | Polymerisation radicalaire d'alcoxyamines a basse temperature |
| BR112017023446A2 (pt) | 2015-04-29 | 2018-07-31 | 3M Innovative Properties Co | método para a fabricação de uma rede polimérica a partir de um politiol e um poliepóxido |
| WO2018085534A1 (en) | 2016-11-03 | 2018-05-11 | 3M Innovative Properties Company | Compositions including a photolatent amine, camphorquinone, and a coumarin and related methods |
| JP2019534363A (ja) | 2016-11-03 | 2019-11-28 | スリーエム イノベイティブ プロパティズ カンパニー | シーラントを航空機用部品に適用する方法 |
| WO2018085190A1 (en) | 2016-11-03 | 2018-05-11 | 3M Innovative Properties Company | Polythiol sealant compositions |
| JP6873417B2 (ja) * | 2016-11-10 | 2021-05-19 | 学校法人東京理科大学 | 光反応性組成物 |
| US20190369494A1 (en) * | 2016-12-05 | 2019-12-05 | Arkemea Inc. | Initiator blends and photocurable compositions containing such initiator blends useful for 3d printing |
| WO2018160691A1 (en) * | 2017-02-28 | 2018-09-07 | Basf Se | Curable sealant composition |
| WO2018160667A1 (en) * | 2017-02-28 | 2018-09-07 | Basf Se | Curable sealant composition |
| GB2567242B (en) * | 2017-10-09 | 2021-08-11 | Henkel IP & Holding GmbH | Anaerobically curable compositions comprising 1, 2, 3, 4-tetrahydro benzo(h)quinolin-3-ol or derivatives thereof |
| CN112752803A (zh) | 2018-09-27 | 2021-05-04 | 3M创新有限公司 | 包含氨基官能硅烷的组合物以及将密封剂施用到基材的方法 |
| CN111040644A (zh) * | 2018-10-15 | 2020-04-21 | 烟台德邦科技有限公司 | 一种可光催化聚合的丙烯酸酯结构胶 |
| WO2020153269A1 (ja) * | 2019-01-21 | 2020-07-30 | 三井化学株式会社 | 光重合開始剤、光硬化性組成物、硬化物、及び、歯科材料 |
| WO2020202076A1 (en) | 2019-04-04 | 2020-10-08 | 3M Innovative Properties Company | Method of irradiating a composition through a substrate |
| WO2023167201A1 (ja) * | 2022-03-02 | 2023-09-07 | 株式会社カネカ | 活性エネルギー線硬化性組成物、及び硬化物の製造方法 |
| WO2024204487A1 (ja) * | 2023-03-30 | 2024-10-03 | 日東シンコー株式会社 | コーティング用硬化性組成物、及び、その硬化物 |
| TWI885621B (zh) * | 2023-11-30 | 2025-06-01 | 國家中山科學研究院 | 乙烯基酯樹脂之固化方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3018266A (en) * | 1960-07-29 | 1962-01-23 | American Cyanamid Co | Polymerizable elastomer-vinyl aromatic compound composition containing a catalyst promoter system and method of polymerizing same |
| DE3612442A1 (de) * | 1986-04-12 | 1987-10-22 | Bayer Ag | Verfahren zur herstellung von uv-gehaerteten deckend pigmentierten beschichtungen |
| JPH1149835A (ja) * | 1997-08-05 | 1999-02-23 | Showa Highpolymer Co Ltd | コンクリート構築物用プライマー組成物及びその硬化方法 |
| TW436491B (en) * | 1997-08-22 | 2001-05-28 | Ciba Sc Holding Ag | Compositions for use in base-catalysed reactions, a process for curing said compostions and a process for photochemically generating bases in base catalysed polymeriaztion reactions |
| EP0898202B1 (en) * | 1997-08-22 | 2000-07-19 | Ciba SC Holding AG | Photogeneration of amines from alpha-aminoacetophenones |
| WO2001092362A1 (en) * | 2000-05-26 | 2001-12-06 | Akzo Nobel N.V. | Photoactivatable coating composition |
| US7538104B2 (en) * | 2001-10-17 | 2009-05-26 | Ciba Specialty Chemicals Corporation | Photoactivable nitrogen bases |
| US6664357B1 (en) * | 2003-01-21 | 2003-12-16 | National Starch And Chemical Investment Holding Corporation | Method for the preparation of a stable anaerobic/UV/visible light curable adhesive |
| EP1789188A2 (en) * | 2004-07-21 | 2007-05-30 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Process for the photoactivation and use of a catalyst by an inverted two-stage procedure |
| DE102005010327A1 (de) * | 2005-03-03 | 2006-09-07 | Basf Ag | Ratikalisch härtbare Beschichtungsmassen |
| JP4967276B2 (ja) * | 2005-08-09 | 2012-07-04 | 日立化成工業株式会社 | 回路接続材料並びに回路端子の接続構造体及び接続方法 |
| RU2009115962A (ru) * | 2006-09-29 | 2010-11-10 | Циба Холдинг Инк. (Ch) | Фотолатентные основания для систем, основанных на блокированных изоцианатах |
-
2009
- 2009-01-06 EP EP09706026.3A patent/EP2238178B1/en not_active Not-in-force
- 2009-01-06 JP JP2010544653A patent/JP5697992B2/ja not_active Expired - Fee Related
- 2009-01-06 WO PCT/EP2009/050066 patent/WO2009095282A2/en not_active Ceased
- 2009-01-06 US US12/812,795 patent/US20110190412A1/en not_active Abandoned
- 2009-01-06 CN CN2009801032825A patent/CN101925616A/zh active Pending
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