GB1355083A - Process for polymerisation of epoxides - Google Patents
Process for polymerisation of epoxidesInfo
- Publication number
- GB1355083A GB1355083A GB2693571*A GB2693571A GB1355083A GB 1355083 A GB1355083 A GB 1355083A GB 2693571 A GB2693571 A GB 2693571A GB 1355083 A GB1355083 A GB 1355083A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- compound
- phosphorus
- alkyl
- plus
- 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.)
- Expired
Links
- 150000002118 epoxides Chemical class 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 13
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 9
- 229910052698 phosphorus Inorganic materials 0.000 abstract 7
- 239000011574 phosphorus Substances 0.000 abstract 7
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 6
- 239000007795 chemical reaction product Substances 0.000 abstract 5
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 abstract 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- -1 alkoxy halide Chemical class 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052794 bromium Inorganic materials 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- 229910052740 iodine Chemical group 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 238000006116 polymerization reaction Methods 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 2
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 abstract 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 150000001983 dialkylethers Chemical class 0.000 abstract 2
- 229910052732 germanium Inorganic materials 0.000 abstract 2
- 229910052735 hafnium Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- 229910052710 silicon Inorganic materials 0.000 abstract 2
- 229910052718 tin Inorganic materials 0.000 abstract 2
- 229910052719 titanium Inorganic materials 0.000 abstract 2
- 229910052726 zirconium Inorganic materials 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 abstract 1
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 229910052786 argon Inorganic materials 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910021480 group 4 element Inorganic materials 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/08—Saturated oxiranes
- C08G65/10—Saturated oxiranes characterised by the catalysts used
- C08G65/12—Saturated oxiranes characterised by the catalysts used containing organo-metallic compounds or metal hydrides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polyethers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP45096044A JPS4911639B1 (enExample) | 1970-10-30 | 1970-10-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1355083A true GB1355083A (en) | 1974-06-05 |
Family
ID=14154467
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2693571*A Expired GB1355083A (en) | 1970-10-30 | 1971-04-19 | Process for polymerisation of epoxides |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3880779A (enExample) |
| JP (1) | JPS4911639B1 (enExample) |
| CA (1) | CA939446A (enExample) |
| DE (1) | DE2120370C3 (enExample) |
| FR (1) | FR2112361B1 (enExample) |
| GB (1) | GB1355083A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111433238A (zh) * | 2017-12-06 | 2020-07-17 | Ａｇｃ株式会社 | 含氟弹性共聚物及含氟弹性共聚物的制造方法 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4011268A (en) * | 1973-08-22 | 1977-03-08 | The Dow Chemical Company | Method of preparing monoethers of alkylene glycols |
| JPS5453336U (enExample) * | 1977-09-22 | 1979-04-13 | ||
| JPS54118753A (en) * | 1978-03-08 | 1979-09-14 | Tokyo Electric Co Ltd | Electronic register |
| JPS564628A (en) * | 1979-06-26 | 1981-01-19 | Nippon Zeon Co Ltd | Production of epihalohydrin copolymer rubber |
| US4293675A (en) * | 1980-02-26 | 1981-10-06 | Minnesota Mining And Manufacturing Company | Antimony halide-organic phosphonate ester cationic polymerization catalysts |
| US20060281894A1 (en) * | 2005-06-13 | 2006-12-14 | Basf Corporation. | Method of forming polyetherols in the presence of aluminum phosphate catalysts |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3018258A (en) * | 1958-06-17 | 1962-01-23 | Shell Oil Co | New curing agents for polyepoxides and method for their preparation |
| GB1236848A (en) * | 1968-09-12 | 1971-06-23 | Kalk Chemische Fabrik Gmbh | Method of preparing transparent products consisting largely of polyepibromohydrin |
| US3657159A (en) * | 1968-10-14 | 1972-04-18 | Hercules Inc | Epoxide polymerization catalysts comprising complex organoaluminate compounds of silicon tin or phosphorus |
-
1970
- 1970-10-30 JP JP45096044A patent/JPS4911639B1/ja active Pending
-
1971
- 1971-04-12 US US133430A patent/US3880779A/en not_active Expired - Lifetime
- 1971-04-14 CA CA110,347A patent/CA939446A/en not_active Expired
- 1971-04-19 GB GB2693571*A patent/GB1355083A/en not_active Expired
- 1971-04-26 DE DE2120370A patent/DE2120370C3/de not_active Expired
- 1971-05-13 FR FR7117377A patent/FR2112361B1/fr not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111433238A (zh) * | 2017-12-06 | 2020-07-17 | Ａｇｃ株式会社 | 含氟弹性共聚物及含氟弹性共聚物的制造方法 |
| CN111433238B (zh) * | 2017-12-06 | 2021-12-10 | Ａｇｃ株式会社 | 含氟弹性共聚物及含氟弹性共聚物的制造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2120370C3 (de) | 1975-05-22 |
| US3880779A (en) | 1975-04-29 |
| DE2120370A1 (de) | 1972-05-10 |
| DE2120370B2 (de) | 1974-08-22 |
| FR2112361B1 (enExample) | 1974-09-06 |
| FR2112361A1 (enExample) | 1972-06-16 |
| CA939446A (en) | 1974-01-01 |
| JPS4911639B1 (enExample) | 1974-03-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PE20 | Patent expired after termination of 20 years |