JP2013516516A5 - - Google Patents
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- Publication number
- JP2013516516A5 JP2013516516A5 JP2012547149A JP2012547149A JP2013516516A5 JP 2013516516 A5 JP2013516516 A5 JP 2013516516A5 JP 2012547149 A JP2012547149 A JP 2012547149A JP 2012547149 A JP2012547149 A JP 2012547149A JP 2013516516 A5 JP2013516516 A5 JP 2013516516A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- aralkyl
- formula
- independently
- aryl
- 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
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 93
- 125000002947 alkylene group Chemical group 0.000 claims description 67
- 125000000217 alkyl group Chemical group 0.000 claims description 60
- 125000003118 aryl group Chemical group 0.000 claims description 60
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 52
- 125000004474 heteroalkylene group Chemical group 0.000 claims description 49
- 125000000623 heterocyclic group Chemical group 0.000 claims description 38
- 229910052739 hydrogen Inorganic materials 0.000 claims description 38
- 239000001257 hydrogen Substances 0.000 claims description 38
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 38
- 125000003107 substituted aryl group Chemical group 0.000 claims description 33
- 229910052757 nitrogen Inorganic materials 0.000 claims description 32
- -1 primary amine compound Chemical class 0.000 claims description 31
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 26
- 229920001577 copolymer Polymers 0.000 claims description 23
- 239000010702 perfluoropolyether Substances 0.000 claims description 23
- 125000000732 arylene group Chemical group 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 22
- 150000001412 amines Chemical class 0.000 claims description 13
- 239000011541 reaction mixture Substances 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 12
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 11
- 125000001188 haloalkyl group Chemical group 0.000 claims description 11
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims 29
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000000047 product Substances 0.000 description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000003682 fluorination reaction Methods 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29108309P | 2009-12-30 | 2009-12-30 | |
| US61/291,083 | 2009-12-30 | ||
| PCT/US2010/061709 WO2011082046A1 (en) | 2009-12-30 | 2010-12-22 | Copolymers with perfluorpolyether segment and multiple aminooxalylamino groups |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013516516A JP2013516516A (ja) | 2013-05-13 |
| JP2013516516A5 true JP2013516516A5 (enExample) | 2015-02-12 |
| JP5777635B2 JP5777635B2 (ja) | 2015-09-09 |
Family
ID=43733351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012547149A Expired - Fee Related JP5777635B2 (ja) | 2009-12-30 | 2010-12-22 | ペルフルオロポリエーテルセグメント及び複数のアミノオキサリルアミノ基を有するコポリマー |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US8907046B2 (enExample) |
| EP (1) | EP2519560B1 (enExample) |
| JP (1) | JP5777635B2 (enExample) |
| CN (1) | CN102770478B (enExample) |
| WO (1) | WO2011082046A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102695712B (zh) * | 2009-12-30 | 2015-11-25 | 3M创新有限公司 | 湿固化硅氧烷和硅氧烷聚合物 |
| CN102695745B (zh) * | 2009-12-30 | 2013-11-13 | 3M创新有限公司 | 具有全氟聚醚链段和聚二有机硅氧烷链段的共聚物 |
| CN102770478B (zh) | 2009-12-30 | 2014-03-12 | 3M创新有限公司 | 具有全氟聚醚链段和多个氨基乙二酰胺基的共聚物 |
| EP2519559B1 (en) * | 2009-12-30 | 2015-07-15 | 3M Innovative Properties Company | Perfluoropolyether-containing compounds with oxalylamino groups |
| KR101788345B1 (ko) * | 2009-12-30 | 2017-10-19 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 습기-경화형 실록산-함유 및 플루오로탄소-함유 화합물 및 그로부터 형성되는 중합체 |
| CN102712758B (zh) | 2009-12-30 | 2014-05-07 | 3M创新有限公司 | 制备聚二有机硅氧烷-聚乙二酰胺共聚物的方法 |
| EP3087119B1 (en) * | 2013-12-24 | 2019-02-27 | Solvay Specialty Polymers Italy S.p.A. | Polyamides modified with (per)fluoropolyether segments |
| US10232078B2 (en) | 2015-12-22 | 2019-03-19 | 3M Innovative Properties Company | Curable polymeric materials and methods of using same |
| US10196548B2 (en) | 2015-12-22 | 2019-02-05 | 3M Innovative Properties Company | Oxalate ester—polyamine thermosetting compositions |
| US12139626B2 (en) * | 2020-01-28 | 2024-11-12 | SOCIéTé BIC | Irreversibly erasable ink composition having a discoloration agent |
| CN119095898A (zh) * | 2022-04-27 | 2024-12-06 | 大金工业株式会社 | 含氟代聚醚基的氧亚烷基酰胺化合物 |
| CN115028666A (zh) * | 2022-07-28 | 2022-09-09 | 上海凌凯医药科技有限公司 | 一种呋喃糖2号位芳基氰基双取代化合物的制备方法 |
Family Cites Families (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2343808A (en) | 1939-05-17 | 1944-03-07 | Schlack Paul | Nitrogenous condensation products |
| US3250807A (en) | 1963-08-23 | 1966-05-10 | Du Pont | Dicarboxylic acids of fluorocarbon ethers and fluorides, esters, amides and salts thereof |
| NL148300B (nl) | 1964-01-02 | 1976-01-15 | Edison Soc | Werkwijze ter bereiding van polyoxyperfluormethylenen. |
| NL6709067A (enExample) | 1964-04-09 | 1968-01-08 | ||
| US3442942A (en) | 1964-04-09 | 1969-05-06 | Montedison Spa | Fluorinated oxygen containing acyl fluorides |
| DE1745169B2 (de) | 1967-02-09 | 1977-04-21 | Montecatini Edison S.P.A., Mailand (Italien) | Fluorierte lineare polyaether und verfahren zu ihrer herstellung |
| US3485806A (en) | 1968-02-07 | 1969-12-23 | Ashland Oil Inc | Hydroxy substituted aminimides |
| US3634362A (en) * | 1969-02-19 | 1972-01-11 | Ici Ltd | Process for the manufacture of polyoxaqides in the presence of a glycol |
| US4085137A (en) | 1969-03-10 | 1978-04-18 | Minnesota Mining And Manufacturing Company | Poly(perfluoroalkylene oxide) derivatives |
| US3810874A (en) | 1969-03-10 | 1974-05-14 | Minnesota Mining & Mfg | Polymers prepared from poly(perfluoro-alkylene oxide) compounds |
| US3728311A (en) | 1971-12-16 | 1973-04-17 | Du Pont | Polyureas,polyurethanes and polyamides based on a tetra-oxo diamine component |
| US3890269A (en) | 1972-08-11 | 1975-06-17 | Stauffer Chemical Co | Process for preparing aminofunctional polysiloxane polymers |
| US4119615A (en) | 1976-09-24 | 1978-10-10 | Texaco Development Corporation | Thermoplastic adhesive polyoxamide from polyoxypropylene polyamine |
| US4684728A (en) | 1979-01-12 | 1987-08-04 | Bayer Aktiengesellschaft | Solubilizing biologically active compounds with reactive hydrogen atoms |
| US4661577A (en) | 1985-10-01 | 1987-04-28 | General Electric Company | Aminofunctional polysiloxanes |
| US5512650A (en) | 1986-06-20 | 1996-04-30 | Minnesota Mining And Manufacturing Company | Block copolymer, method of making the same, diamine precursors of the same, method of making such diamines and end products comprising the block copolymer |
| US5214119A (en) | 1986-06-20 | 1993-05-25 | Minnesota Mining And Manufacturing Company | Block copolymer, method of making the same, dimaine precursors of the same, method of making such diamines and end products comprising the block copolymer |
| US5026890A (en) | 1988-05-20 | 1991-06-25 | General Electric Company | Method and intermediates for preparation of bis(aminoalkyl)polydiorganosiloxanes |
| US5093432A (en) | 1988-09-28 | 1992-03-03 | Exfluor Research Corporation | Liquid phase fluorination |
| US5266650A (en) | 1990-10-11 | 1993-11-30 | Minnesota Mining And Manufacturing Company | Curing fluorocarbon elastomers |
| JP2684130B2 (ja) | 1991-08-15 | 1997-12-03 | 信越化学工業株式会社 | アミノ基含有ポリシロキサンの製造方法 |
| US5488142A (en) | 1993-10-04 | 1996-01-30 | Minnesota Mining And Manufacturing Company | Fluorination in tubular reactor system |
| US5663127A (en) | 1994-07-29 | 1997-09-02 | Minnesota Mining And Manufacturing Company | Perfluoropolyether lubricating compositions |
| DE69629189T2 (de) | 1995-04-25 | 2004-06-03 | Minnesota Mining And Mfg. Co., Saint Paul | Segmentierte polydiorganosiloxan-oligoharnstoff-copolymere sowie verfahren zu deren herstellung |
| US6355759B1 (en) | 1996-04-25 | 2002-03-12 | 3M Innovative Properties Company | Polydiorganosiloxane polyurea segmented copolymers and a process for making same |
| US6313335B1 (en) | 1997-11-25 | 2001-11-06 | 3M Innovative Properties | Room temperature curable silane terminated and stable waterborne polyurethane dispersions which contain fluorine and/or silicone and low surface energy coatings prepared therefrom |
| JP3729687B2 (ja) | 1999-08-04 | 2005-12-21 | 株式会社巴川製紙所 | 反射防止材料 |
| ITMI20021734A1 (it) * | 2002-08-01 | 2004-02-02 | Ausimont S P A Ora Solvay Solexis Spa | Processo per la preparazione di perfluoropolieteri con terminali aldeidici, alcolici, amminici mediante riduzione catalitica. |
| TWI293715B (en) | 2002-10-10 | 2008-02-21 | Sipix Imaging Inc | A method for inducing or enhancing the threshold of an electrophoretic display, an electrophoretic fluid and an electrophoretic display |
| US6923921B2 (en) | 2002-12-30 | 2005-08-02 | 3M Innovative Properties Company | Fluorinated polyether compositions |
| US20040266985A1 (en) | 2003-06-26 | 2004-12-30 | Jon Lee Howell | Nitrogenated perfluoropolyether composition |
| US7288619B2 (en) | 2004-05-07 | 2007-10-30 | 3M Innovative Properties Company | Fluorinated polyether polyamine and method of making the same |
| US20070149745A1 (en) | 2005-12-23 | 2007-06-28 | 3M Innovative Properties Company | Polydiorganosiloxane-containing materials with oxalylamino groups |
| US7501184B2 (en) | 2005-12-23 | 2009-03-10 | 3M Innovative Properties Company | Polydiorganosiloxane polyoxamide copolymers |
| US8067094B2 (en) | 2005-12-23 | 2011-11-29 | 3M Innovative Properties Company | Films including thermoplastic silicone block copolymers |
| US7371464B2 (en) | 2005-12-23 | 2008-05-13 | 3M Innovative Properties Company | Adhesive compositions |
| BRPI0706862A2 (pt) | 2006-01-13 | 2011-04-12 | Du Pont | composições, método de produção de refrigeração, método de produção de calor, processo de transferência de calor, processo de substituição de refrigerante ou fluido de transferência de calor, aparelho de refrigeração, aparelho de ar condicionado e aparelho de bomba de aquecimento com superfìcies de transferência de calor |
| WO2008027594A2 (en) | 2006-09-01 | 2008-03-06 | E. I. Du Pont De Nemours And Company | Phenol stabilizers for fluoroolefins |
| EP2096133A4 (en) | 2006-12-11 | 2012-07-04 | Ube Industries | POLYAMIDE RESIN |
| US7745653B2 (en) | 2007-03-08 | 2010-06-29 | 3M Innovative Properties Company | Fluorochemical compounds having pendent silyl groups |
| US7335786B1 (en) | 2007-03-29 | 2008-02-26 | 3M Innovative Properties Company | Michael-adduct fluorochemical silanes |
| US8063166B2 (en) | 2007-06-22 | 2011-11-22 | 3M Innovative Properties Company | Polydiorganosiloxane polyamide copolymers having organic soft segments |
| US7705101B2 (en) | 2007-06-22 | 2010-04-27 | 3M Innovative Properties Company | Branched polydiorganosiloxane polyamide copolymers |
| CN102695745B (zh) * | 2009-12-30 | 2013-11-13 | 3M创新有限公司 | 具有全氟聚醚链段和聚二有机硅氧烷链段的共聚物 |
| EP2519559B1 (en) | 2009-12-30 | 2015-07-15 | 3M Innovative Properties Company | Perfluoropolyether-containing compounds with oxalylamino groups |
| CN102712758B (zh) | 2009-12-30 | 2014-05-07 | 3M创新有限公司 | 制备聚二有机硅氧烷-聚乙二酰胺共聚物的方法 |
| CN102770478B (zh) * | 2009-12-30 | 2014-03-12 | 3M创新有限公司 | 具有全氟聚醚链段和多个氨基乙二酰胺基的共聚物 |
| JPWO2012036303A1 (ja) * | 2010-09-17 | 2014-02-03 | 宇部興産株式会社 | 耐衝撃性に優れるポリオキサミド樹脂及び耐衝撃性部品 |
-
2010
- 2010-12-22 CN CN201080064616.5A patent/CN102770478B/zh not_active Expired - Fee Related
- 2010-12-22 JP JP2012547149A patent/JP5777635B2/ja not_active Expired - Fee Related
- 2010-12-22 US US13/514,661 patent/US8907046B2/en not_active Expired - Fee Related
- 2010-12-22 WO PCT/US2010/061709 patent/WO2011082046A1/en not_active Ceased
- 2010-12-22 EP EP10801529.8A patent/EP2519560B1/en not_active Not-in-force
-
2014
- 2014-10-30 US US14/528,827 patent/US9279035B2/en active Active
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