JP2011519382A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2011519382A5 JP2011519382A5 JP2011501293A JP2011501293A JP2011519382A5 JP 2011519382 A5 JP2011519382 A5 JP 2011519382A5 JP 2011501293 A JP2011501293 A JP 2011501293A JP 2011501293 A JP2011501293 A JP 2011501293A JP 2011519382 A5 JP2011519382 A5 JP 2011519382A5
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- group
- formula
- alkoxide
- complexes
- 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
- 229920000642 polymer Polymers 0.000 claims 31
- -1 lactone compound Chemical class 0.000 claims 20
- 238000000034 method Methods 0.000 claims 17
- 239000003999 initiator Substances 0.000 claims 7
- 238000006116 polymerization reaction Methods 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 229910052725 zinc Inorganic materials 0.000 claims 5
- 239000011701 zinc Substances 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 150000005676 cyclic carbonates Chemical class 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 229920005565 cyclic polymer Polymers 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 239000003446 ligand Substances 0.000 claims 3
- 229910052751 metal Inorganic materials 0.000 claims 3
- 239000002184 metal Substances 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- 150000004703 alkoxides Chemical class 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 239000000835 fiber Substances 0.000 claims 2
- 150000002596 lactones Chemical class 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000005022 packaging material Substances 0.000 claims 2
- 229920005604 random copolymer Polymers 0.000 claims 2
- 238000007142 ring opening reaction Methods 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 150000003973 alkyl amines Chemical class 0.000 claims 1
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- 239000003849 aromatic solvent Substances 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
- 229920001400 block copolymer Polymers 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims 1
- 229930188620 butyrolactone Natural products 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 238000004581 coalescence Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000005265 dialkylamine group Chemical group 0.000 claims 1
- 150000002009 diols Chemical group 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- RWZKAROCZDFJEI-UHFFFAOYSA-N ethanol;zinc Chemical group [Zn].CCO.CCO RWZKAROCZDFJEI-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 229920000578 graft copolymer Polymers 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 239000007943 implant Substances 0.000 claims 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical group CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 claims 1
- 229910052746 lanthanum Inorganic materials 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 claims 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 229910001407 tin (II) carbonate Inorganic materials 0.000 claims 1
- UNYGOTXWMGACLR-UHFFFAOYSA-L tin(2+);carbonate Chemical compound [Sn+2].[O-]C([O-])=O UNYGOTXWMGACLR-UHFFFAOYSA-L 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 239000010936 titanium Substances 0.000 claims 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical group O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 claims 1
- 229910052727 yttrium Inorganic materials 0.000 claims 1
- 229910052726 zirconium Inorganic materials 0.000 claims 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims 1
- 0 *C(CC1O*)C(*)OC1=O Chemical compound *C(CC1O*)C(*)OC1=O 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0805701.0A GB0805701D0 (en) | 2008-03-28 | 2008-03-28 | Polymerization of a carbohydrate lactone |
| GB0805701.0 | 2008-03-28 | ||
| PCT/GB2009/000825 WO2009118538A2 (en) | 2008-03-28 | 2009-03-27 | Carbohydrate lactone polymers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011519382A JP2011519382A (ja) | 2011-07-07 |
| JP2011519382A5 true JP2011519382A5 (enExample) | 2012-05-10 |
| JP5719286B2 JP5719286B2 (ja) | 2015-05-13 |
Family
ID=39386945
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011501293A Expired - Fee Related JP5719286B2 (ja) | 2008-03-28 | 2009-03-27 | 炭水化物ラクトン重合体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8476402B2 (enExample) |
| EP (1) | EP2268701B1 (enExample) |
| JP (1) | JP5719286B2 (enExample) |
| CN (1) | CN102015824A (enExample) |
| BR (1) | BRPI0906316A2 (enExample) |
| CA (1) | CA2719375A1 (enExample) |
| GB (1) | GB0805701D0 (enExample) |
| WO (1) | WO2009118538A2 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2253637A1 (en) * | 2009-04-30 | 2010-11-24 | Total Petrochemicals Research Feluy | Catalytic systems for immortal ring-opening polymerisation of cyclic esters and cyclic carbonates |
| BE1019059A3 (fr) | 2009-12-03 | 2012-02-07 | Futerro Sa | Procede de polymerisation en masse du lactide. |
| WO2012160042A1 (en) * | 2011-05-23 | 2012-11-29 | Total Research & Technology Feluy | Process for the polymerization of cyclic carbonates |
| WO2013186313A1 (en) * | 2012-06-15 | 2013-12-19 | Total Research & Technology Feluy | Method of copolymerizing ethylene carbonate with one or more cyclic esters |
| EP2992032B1 (en) * | 2013-04-29 | 2017-12-06 | Total Research & Technology Feluy | Process for preparing polycarbonates by polymerization of five-membered-ring cyclic carbonates |
| WO2017010250A1 (ja) * | 2015-07-16 | 2017-01-19 | テルモ株式会社 | 生分解性ステント基体を有するステント |
| CN107057045B (zh) * | 2017-01-19 | 2020-04-14 | 四川大学 | 一种葡萄糖衍生物内酯-环状内酯聚合物及其制备方法 |
| CN107163231B (zh) * | 2017-05-04 | 2019-09-24 | 绍兴文理学院 | 一种生物降解聚酯纳米粒及其制备方法和应用 |
| EP3699175B1 (en) | 2019-02-19 | 2022-05-04 | Kemijski Institut | Functionalized aliphatic polyesters and process for producing the same |
| CN110317563B (zh) * | 2019-07-08 | 2020-06-09 | 中国水利水电科学研究院 | 一种复合聚酯热熔胶、制备方法及抗冲刷土工布的制备方法 |
| CN118994077A (zh) * | 2024-08-09 | 2024-11-22 | 中国科学院长春应用化学研究所 | 一种双取代六元环酯及其制备方法和在制备可闭环回收聚酯中的应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3301825A (en) * | 1963-09-26 | 1967-01-31 | Union Carbide Corp | Polyester polycarbonate polymers |
| JPS63258872A (ja) * | 1987-04-16 | 1988-10-26 | Mitsubishi Rayon Co Ltd | バレロラクトン誘導体 |
| US5124069A (en) | 1989-03-16 | 1992-06-23 | Mitsubishi Rayon Company Ltd. | Optically active substance and liquid crystal composition comprising same |
| DE69118261T2 (de) * | 1990-07-20 | 1996-12-05 | Mitsubishi Rayon Co | Optisch aktive Delta-Valerolacton-Ring enthaltende Verbindung und dieselbe enthaltende flüssigkristalline Zusammensetzung |
| JP3450810B2 (ja) * | 2000-01-31 | 2003-09-29 | キヤノン株式会社 | 脂肪族ポリエステル、脂肪族ポリエステルの製造方法およびセルロースの再資源化方法 |
| JP2002167430A (ja) | 2000-12-01 | 2002-06-11 | Canon Inc | 脂肪族ポリエステル、脂肪族ポリエステルの製造方法およびデンプンの資源化方法 |
-
2008
- 2008-03-28 GB GBGB0805701.0A patent/GB0805701D0/en not_active Ceased
-
2009
- 2009-03-27 WO PCT/GB2009/000825 patent/WO2009118538A2/en not_active Ceased
- 2009-03-27 CN CN2009801123608A patent/CN102015824A/zh active Pending
- 2009-03-27 US US12/934,719 patent/US8476402B2/en not_active Expired - Fee Related
- 2009-03-27 CA CA2719375A patent/CA2719375A1/en not_active Abandoned
- 2009-03-27 EP EP09725730.7A patent/EP2268701B1/en not_active Not-in-force
- 2009-03-27 BR BRPI0906316-1A patent/BRPI0906316A2/pt not_active IP Right Cessation
- 2009-03-27 JP JP2011501293A patent/JP5719286B2/ja not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2011519382A5 (enExample) | ||
| Dechy-Cabaret et al. | Controlled ring-opening polymerization of lactide and glycolide | |
| JP5952264B2 (ja) | ペンタフルオロフェニルエステルペンダント基を有するポリマー並びにその合成及び機能付与の方法 | |
| JP5943491B2 (ja) | ポリエステルを調製するプロセス | |
| Zhao et al. | Facile synthesis of hydroxyl-ended, highly stereoregular, star-shaped poly (lactide) from immortal ROP of rac-lactide and kinetics study | |
| CN102596973B (zh) | 有机锡化合物、其制备方法及使用该有机锡化合物制备聚交酯的方法 | |
| RU2010106198A (ru) | Органополисилоксан | |
| JP2019108547A (ja) | ５員環カーボナートの重合によるポリカーボネート樹脂の製造方法 | |
| JP5567581B2 (ja) | 高純度ポリ乳酸、その塩またはその誘導体、及びその精製方法 | |
| JP2009046466A5 (enExample) | ||
| Daneshmand et al. | Catalytic-site-mediated chain-end control in the polymerization of rac-lactide with copper iminopyrrolide complexes | |
| US11613605B2 (en) | Block copolymers of cyclic esters and processes for preparing same | |
| DK2640767T3 (en) | Process for preparing polymers of varied architecture and amide initiation | |
| ES2728002T3 (es) | Procedimiento de fabricación de PLA usando un nuevo catalizador de polimerización | |
| CN107298673B (zh) | ε-己内酯衍生物及其制备方法和应用 | |
| Trinca et al. | Influence of the synthesis conditions on the structural and thermal properties of poly (l‐lactide)‐b‐poly (ethylene glycol)‐b‐poly (l‐lactide) | |
| CN101817923A (zh) | 一种催化引发体系 | |
| CN1706878A (zh) | 无金属n－杂环卡宾催化剂及其制备方法 | |
| CN101550126B (zh) | ε-己内酯衍生物及其聚合物 | |
| DE60129252D1 (de) | Bioabbaubare polyester-mischzusammensetzungen und verfahren zu ihrer herstellung | |
| CN116333288B (zh) | 一种氨基喹啉金属铝催化剂的制备方法及其合成可降解高分子材料的应用 | |
| JP6163929B2 (ja) | ホスホリルコリン基含有重合体及びその製造方法 | |
| JP2022064192A (ja) | グラフト共重合体及びその製造方法 | |
| JP2023126174A (ja) | ポリマー化合物、その柔軟性を変化させる方法、それを用いた樹脂の成型方法及び可溶化方法、モノマー化合物、並びにそれを含む重合性組成物 | |
| CN105622954A (zh) | 一种聚乙烯醇-聚肽-聚三亚甲基碳酸酯-聚乳酸乙醇酸三接枝共聚物的制备方法 |