JP2017509772A5 - - Google Patents
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- JP2017509772A5 JP2017509772A5 JP2016560502A JP2016560502A JP2017509772A5 JP 2017509772 A5 JP2017509772 A5 JP 2017509772A5 JP 2016560502 A JP2016560502 A JP 2016560502A JP 2016560502 A JP2016560502 A JP 2016560502A JP 2017509772 A5 JP2017509772 A5 JP 2017509772A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- optionally substituted
- composition
- independently selected
- aliphatic
- 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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- 239000000203 mixture Substances 0.000 claims description 58
- 125000001931 aliphatic group Chemical group 0.000 claims description 33
- 125000005842 heteroatom Chemical group 0.000 claims description 28
- 229920000515 polycarbonate Polymers 0.000 claims description 22
- 239000004417 polycarbonate Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 18
- 125000004429 atom Chemical group 0.000 claims description 15
- 229920005862 polyol Polymers 0.000 claims description 14
- 150000003077 polyols Chemical class 0.000 claims description 14
- 125000003107 substituted aryl group Chemical group 0.000 claims description 12
- -1 cyclic acid anhydride Chemical class 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 239000011737 fluorine Substances 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 6
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 239000003431 cross linking reagent Substances 0.000 claims description 3
- 239000012948 isocyanate Substances 0.000 claims description 3
- 239000004814 polyurethane Substances 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 26
- 229910052757 nitrogen Inorganic materials 0.000 claims 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 13
- 229910052717 sulfur Inorganic materials 0.000 claims 13
- 239000011593 sulfur Substances 0.000 claims 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 12
- 239000001301 oxygen Substances 0.000 claims 12
- 125000004432 carbon atom Chemical group C* 0.000 claims 11
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 10
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 229920000379 polypropylene carbonate Polymers 0.000 claims 6
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 4
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 150000002924 oxiranes Chemical class 0.000 claims 4
- 150000005676 cyclic carbonates Chemical class 0.000 claims 3
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical group ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- 150000004820 halides Chemical group 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 229940014800 succinic anhydride Drugs 0.000 claims 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- FYNXDGNCEBQLGC-UHFFFAOYSA-N CC(C)(C)C1=CC(C(C)(C)C)=CC(C=NC2C(CCCC2)N=CC=2C(=C(C=C(C=2)C(C)(C)C)C(C)(C)C)O)=C1O Chemical group CC(C)(C)C1=CC(C(C)(C)C)=CC(C=NC2C(CCCC2)N=CC=2C(=C(C=C(C=2)C(C)(C)C)C(C)(C)C)O)=C1O FYNXDGNCEBQLGC-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 150000004703 alkoxides Chemical group 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 150000007942 carboxylates Chemical group 0.000 claims 1
- 239000012986 chain transfer agent Substances 0.000 claims 1
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical group [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 claims 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 claims 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- SCRKTTJILRGIEY-UHFFFAOYSA-N pentanedioic acid;zinc Chemical compound [Zn].OC(=O)CCCC(O)=O SCRKTTJILRGIEY-UHFFFAOYSA-N 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- YNHJECZULSZAQK-UHFFFAOYSA-N tetraphenylporphyrin Chemical compound C1=CC(C(=C2C=CC(N2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3N2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 YNHJECZULSZAQK-UHFFFAOYSA-N 0.000 claims 1
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 claims 1
- 239000004246 zinc acetate Substances 0.000 claims 1
- 0 CC1C(*)CCC1 Chemical compound CC1C(*)CCC1 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 2
- UHBWJBFBNRSVEY-UHFFFAOYSA-N (carbamoylamino) 3-oxobutanoate formaldehyde Chemical compound O=C.CC(=O)CC(=O)ONC(N)=O UHBWJBFBNRSVEY-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461974500P | 2014-04-03 | 2014-04-03 | |
| US61/974,500 | 2014-04-03 | ||
| PCT/US2015/024299 WO2015154001A1 (en) | 2014-04-03 | 2015-04-03 | Aliphatic polycarbonate polyol compositions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017509772A JP2017509772A (ja) | 2017-04-06 |
| JP2017509772A5 true JP2017509772A5 (https=) | 2018-08-16 |
| JP6900194B2 JP6900194B2 (ja) | 2021-07-07 |
Family
ID=52988466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016560502A Active JP6900194B2 (ja) | 2014-04-03 | 2015-04-03 | 脂肪族ポリカーボネートポリオール組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10308759B2 (https=) |
| EP (1) | EP3126424B1 (https=) |
| JP (1) | JP6900194B2 (https=) |
| KR (1) | KR102392235B1 (https=) |
| CN (1) | CN106661215B (https=) |
| ES (1) | ES2837861T3 (https=) |
| WO (1) | WO2015154001A1 (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9738760B2 (en) | 2013-05-01 | 2017-08-22 | Novomer, Inc. | Aliphatic polycarbonate compositions and methods |
| US10053533B1 (en) * | 2017-04-13 | 2018-08-21 | Presidium Usa, Inc. | Oligomeric polyol compositions |
| JP2021522355A (ja) | 2018-04-18 | 2021-08-30 | サウジ アラムコ テクノロジーズ カンパニー | ポリ（アルキレンカーボネート）ポリマーの末端基異性化 |
| WO2020028606A1 (en) | 2018-08-02 | 2020-02-06 | Saudi Aramco Technologies Company | Sustainable polymer compositions and methods |
| MA53727A (fr) | 2018-09-24 | 2021-12-29 | Saudi Aramco Tech Co | Copolymères séquencés de polycarbonate et procédés associés |
| CN110105559A (zh) * | 2019-05-16 | 2019-08-09 | 岭南师范学院 | 一步制备交联二氧化碳共聚物的方法 |
| GB202017531D0 (en) | 2020-11-05 | 2020-12-23 | Econic Tech Limited | (poly)ol block copolymer |
| US12195576B2 (en) | 2021-06-23 | 2025-01-14 | Saudi Aramco Technologies Company | Polyol compositions and methods |
| CN113773478B (zh) * | 2021-09-26 | 2022-09-06 | 中国科学院长春应用化学研究所 | 一种聚(碳酸酯-醚)基生物降解聚酯及其制备方法 |
| CN114763431A (zh) * | 2021-12-08 | 2022-07-19 | 山东联欣环保科技有限公司 | 一种抗冲击能力强的复合高分子材料及其制备方法 |
| CN116355195B (zh) * | 2023-01-09 | 2024-11-29 | 中山大学 | 一种脂肪族聚碳酸酯多元醇的制备方法 |
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| US5665890A (en) | 1995-03-14 | 1997-09-09 | President And Fellows Of Harvard College | Stereoselective ring opening reactions |
| TWI246520B (en) | 1997-04-25 | 2006-01-01 | Mitsui Chemicals Inc | Processes for olefin polymerization |
| US6130340A (en) | 1998-01-13 | 2000-10-10 | President And Fellows Of Harvard College | Asymmetric cycloaddition reactions |
| US6521561B1 (en) | 1998-05-01 | 2003-02-18 | President And Fellows Of Harvard College | Main-group metal based asymmetric catalysts and applications thereof |
| KR100342659B1 (en) | 2000-12-15 | 2002-07-04 | Rstech Co Ltd | Chiral polymer salene catalyst and process for preparing chiral compounds from racemic epoxide using the same |
| US6884750B2 (en) | 2001-06-27 | 2005-04-26 | Rs Tech Corp. | Chiral salen catalyst and methods for the preparation of chiral compounds from racemic epoxides by using new catalyst |
| US6639087B2 (en) | 2001-08-22 | 2003-10-28 | Rhodia Pharma Solutions Inc. | Kinetic resolution method |
| DE10235316A1 (de) | 2002-08-01 | 2004-02-12 | Basf Ag | Katalysator und Verfahren zur Carbonylierung von Oxiranen |
| JP4290414B2 (ja) * | 2002-11-20 | 2009-07-08 | 旭化成ケミカルズ株式会社 | 末端封止ポリカーボネート及びその方法 |
| US7304172B2 (en) | 2004-10-08 | 2007-12-04 | Cornell Research Foundation, Inc. | Polycarbonates made using highly selective catalysts |
| KR100724550B1 (ko) | 2004-12-16 | 2007-06-04 | 주식회사 엘지화학 | 이중 금속 아연 착화합물과 이를 촉매로 사용한폴리카보네이트의 제조 방법 |
| WO2006099162A2 (en) | 2005-03-14 | 2006-09-21 | Georgia Tech Research Corporation | Polymeric salen compounds and methods thereof |
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| CN105229047B (zh) | 2012-11-07 | 2018-07-20 | 沙特阿美技术公司 | 高强度聚氨酯泡沫组合物及方法 |
| HK1223388A1 (zh) | 2013-05-13 | 2017-07-28 | Saudi Aramco Technologies Company | 含co2的泡沫和相关方法 |
-
2015
- 2015-04-03 US US15/301,095 patent/US10308759B2/en active Active
- 2015-04-03 JP JP2016560502A patent/JP6900194B2/ja active Active
- 2015-04-03 KR KR1020167030077A patent/KR102392235B1/ko active Active
- 2015-04-03 ES ES15717360T patent/ES2837861T3/es active Active
- 2015-04-03 WO PCT/US2015/024299 patent/WO2015154001A1/en not_active Ceased
- 2015-04-03 EP EP15717360.0A patent/EP3126424B1/en active Active
- 2015-04-03 CN CN201580025859.0A patent/CN106661215B/zh active Active
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