JP2016512857A5 - - Google Patents
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- JP2016512857A5 JP2016512857A5 JP2016503756A JP2016503756A JP2016512857A5 JP 2016512857 A5 JP2016512857 A5 JP 2016512857A5 JP 2016503756 A JP2016503756 A JP 2016503756A JP 2016503756 A JP2016503756 A JP 2016503756A JP 2016512857 A5 JP2016512857 A5 JP 2016512857A5
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- JP
- Japan
- Prior art keywords
- atoms
- optionally substituted
- cyclic ester
- ring size
- group
- 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.)
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- 238000000034 method Methods 0.000 claims 15
- -1 cyclic ester Chemical class 0.000 claims 13
- 229910052727 yttrium Inorganic materials 0.000 claims 12
- 125000004429 atom Chemical group 0.000 claims 10
- 229920001577 copolymer Polymers 0.000 claims 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims 5
- 125000003107 substituted aryl group Chemical group 0.000 claims 5
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- 150000004820 halides Chemical class 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 229910052751 metal Inorganic materials 0.000 claims 3
- 239000002184 metal Substances 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N 2,2-dimethylbutane Chemical compound CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 claims 2
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical compound CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 claims 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 claims 2
- PFEOZHBOMNWTJB-UHFFFAOYSA-N 3-methylpentane Chemical compound CCC(C)CC PFEOZHBOMNWTJB-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 150000004703 alkoxides Chemical class 0.000 claims 2
- 229910052782 aluminium Inorganic materials 0.000 claims 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 150000007942 carboxylates Chemical class 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 150000002596 lactones Chemical group 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 2
- 229910052698 phosphorus Inorganic materials 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- 229910052706 scandium Inorganic materials 0.000 claims 2
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 150000007944 thiolates Chemical class 0.000 claims 2
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- SDTMFDGELKWGFT-UHFFFAOYSA-N 2-methylpropan-2-olate Chemical compound CC(C)(C)[O-] SDTMFDGELKWGFT-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 239000004952 Polyamide Substances 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 150000001540 azides Chemical class 0.000 claims 1
- WRMFBHHNOHZECA-UHFFFAOYSA-N butan-2-olate Chemical compound CCC(C)[O-] WRMFBHHNOHZECA-UHFFFAOYSA-N 0.000 claims 1
- AIXAANGOTKPUOY-UHFFFAOYSA-N carbachol Chemical group [Cl-].C[N+](C)(C)CCOC(N)=O AIXAANGOTKPUOY-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 229910052804 chromium Inorganic materials 0.000 claims 1
- 239000011651 chromium Substances 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 claims 1
- 239000010941 cobalt Substances 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 150000001913 cyanates Chemical class 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 150000003949 imides Chemical class 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 239000003446 ligand Substances 0.000 claims 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 1
- NBTOZLQBSIZIKS-UHFFFAOYSA-N methoxide Chemical compound [O-]C NBTOZLQBSIZIKS-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 239000011574 phosphorus Chemical group 0.000 claims 1
- 229920002647 polyamide Polymers 0.000 claims 1
- 229920000515 polycarbonate Polymers 0.000 claims 1
- 239000004417 polycarbonate Substances 0.000 claims 1
- 229920000728 polyester Polymers 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000005374 siloxide group Chemical group 0.000 claims 1
- 238000001542 size-exclusion chromatography Methods 0.000 claims 1
- 239000011593 sulfur Chemical group 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical group C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 150000003567 thiocyanates Chemical class 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 239000010936 titanium Substances 0.000 claims 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical compound CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052720 vanadium Inorganic materials 0.000 claims 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13001358 | 2013-03-18 | ||
| EP13001358.4 | 2013-03-18 | ||
| PCT/IB2014/059897 WO2014147546A1 (en) | 2013-03-18 | 2014-03-17 | Process for preparing a copolymer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016512857A JP2016512857A (ja) | 2016-05-09 |
| JP2016512857A5 true JP2016512857A5 (enExample) | 2017-02-23 |
Family
ID=47901748
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016503756A Pending JP2016512857A (ja) | 2013-03-18 | 2014-03-17 | コポリマーを調製する方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9512268B2 (enExample) |
| EP (1) | EP2976375B1 (enExample) |
| JP (1) | JP2016512857A (enExample) |
| KR (1) | KR20150132552A (enExample) |
| CN (1) | CN105143303A (enExample) |
| BR (1) | BR112015019566A2 (enExample) |
| WO (1) | WO2014147546A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112015030625A2 (pt) | 2013-06-20 | 2017-07-25 | Saudi Basic Ind Corp | poliésteres do tipo pe |
| US10450450B2 (en) | 2015-05-22 | 2019-10-22 | Sabic Global Technologies B.V. | Polyester block compatibilizer for polyethylene polypropylene blends |
| JP6807336B2 (ja) | 2015-05-22 | 2021-01-06 | サビック グローバル テクノロジーズ ベスローテン フェンノートシャップ | 改良された異相ポリプロピレン |
| US10557026B2 (en) | 2015-05-22 | 2020-02-11 | Sabic Global Technologies B.V. | Composition comprising polypropylene, polyethylene, and a compatilizer |
| US10144802B2 (en) * | 2016-12-05 | 2018-12-04 | Novomer, Inc. | Beta-propiolactone based copolymers containing biogenic carbon, methods for their production and uses thereof |
| US20220267550A1 (en) | 2019-08-18 | 2022-08-25 | Sabic Global Technologies B.V. | Use of a composition for the manufacture of a foamed article |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2535562A1 (de) | 1975-08-08 | 1977-02-17 | Wolfgang Dr Ast | Ungesaettigte polyester-kautschuk- copolymerisate und verfahren zu ihrer herstellung |
| JP3408347B2 (ja) | 1994-06-08 | 2003-05-19 | 高砂香料工業株式会社 | 光学活性ブロック共重合ポリエステル及びその製造方法 |
| US6262278B1 (en) * | 1995-03-14 | 2001-07-17 | President And Fellows Of Harvard College | Stereoselective ring opening reactions |
| WO1999061082A1 (en) | 1998-05-28 | 1999-12-02 | Gunze Limited | Lactide-containing polymer and medical material |
| JP4770092B2 (ja) * | 2001-08-24 | 2011-09-07 | 財団法人名古屋産業科学研究所 | ラクトンの開環重合用触媒、ポリエステルの製造方法、及びブロック共重合体の製造方法。 |
| GB0305927D0 (en) | 2003-03-14 | 2003-04-23 | Ic Innovations Ltd | Compound |
| CN1212343C (zh) * | 2003-11-27 | 2005-07-27 | 中国科学院长春应用化学研究所 | 环酯开环聚合催化剂及制备方法 |
| DE102005017049A1 (de) * | 2005-04-12 | 2006-10-19 | Basf Ag | Verfahren zur Herstellung von Polyhydroxyalkanoaten |
| US7915375B2 (en) | 2006-03-01 | 2011-03-29 | Firestone Polymers, Llc | Metathesis interpolymers having terminal functional group(s) |
| CN101583650B (zh) | 2006-11-14 | 2012-01-18 | 巴斯夫欧洲公司 | 高度支化或超支化聚酯及其生产和应用 |
| DE102008055870A1 (de) | 2008-10-31 | 2010-05-06 | Gkss-Forschungszentrum Geesthacht Gmbh | Multiphasen Polymernetzwerk mit Triple-Shape-Eigenschaften und Formgedächtniseffekt |
| WO2010110460A1 (ja) * | 2009-03-27 | 2010-09-30 | 国立大学法人名古屋大学 | ラクチド・ε－カプロラクトン共重合体の製造方法 |
| BR112013012108A2 (pt) * | 2010-11-18 | 2017-11-07 | Saudi Basic Ind Corp | processo para a preparação de um poliéster |
| CN102617369B (zh) | 2012-02-17 | 2014-10-15 | 华东理工大学 | 类salan单酚类配体金属络合物及其制备方法与应用 |
| US9080012B2 (en) | 2013-07-10 | 2015-07-14 | Xerox Corporation | One-pot, neat ring opening polymerization to prepare resin |
-
2014
- 2014-03-17 KR KR1020157030041A patent/KR20150132552A/ko not_active Withdrawn
- 2014-03-17 EP EP14718751.2A patent/EP2976375B1/en not_active Not-in-force
- 2014-03-17 JP JP2016503756A patent/JP2016512857A/ja active Pending
- 2014-03-17 CN CN201480016425.XA patent/CN105143303A/zh active Pending
- 2014-03-17 US US14/766,254 patent/US9512268B2/en not_active Expired - Fee Related
- 2014-03-17 WO PCT/IB2014/059897 patent/WO2014147546A1/en not_active Ceased
- 2014-03-17 BR BR112015019566A patent/BR112015019566A2/pt not_active IP Right Cessation