GB826787A - Mixed anhydrides and their use as catalysts for the polymerisation of ethylenically unsaturated compounds - Google Patents
Mixed anhydrides and their use as catalysts for the polymerisation of ethylenically unsaturated compoundsInfo
- Publication number
- GB826787A GB826787A GB10532/57A GB1053257A GB826787A GB 826787 A GB826787 A GB 826787A GB 10532/57 A GB10532/57 A GB 10532/57A GB 1053257 A GB1053257 A GB 1053257A GB 826787 A GB826787 A GB 826787A
- Authority
- GB
- United Kingdom
- Prior art keywords
- allyl
- vinyl
- mixed anhydrides
- acid
- anhydrides
- 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
- 150000008064 anhydrides Chemical class 0.000 title abstract 5
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 239000003054 catalyst Substances 0.000 title abstract 2
- NFMHSPWHNQRFNR-UHFFFAOYSA-N hyponitrous acid Chemical compound ON=NO NFMHSPWHNQRFNR-UHFFFAOYSA-N 0.000 abstract 6
- -1 &c. Chemical group 0.000 abstract 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
- IGDLZDCWMRPMGL-UHFFFAOYSA-N 2-ethenylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C=C)C(=O)C2=C1 IGDLZDCWMRPMGL-UHFFFAOYSA-N 0.000 abstract 1
- BQHQZFUAEAVJRE-UHFFFAOYSA-N 2-fluorobuta-1,3-diene Chemical compound FC(=C)C=C BQHQZFUAEAVJRE-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical class C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 abstract 1
- 239000012986 chain transfer agent Substances 0.000 abstract 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical class FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- 229910052745 lead Inorganic materials 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 150000003440 styrenes Chemical class 0.000 abstract 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 1
- 229910052716 thallium Inorganic materials 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/04—Azo-compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE566277D BE566277A (en:Method) | 1957-04-01 | ||
| NL270779D NL270779A (en:Method) | 1957-04-01 | ||
| GB10532/57A GB826787A (en) | 1957-04-01 | 1957-04-01 | Mixed anhydrides and their use as catalysts for the polymerisation of ethylenically unsaturated compounds |
| US723645A US2951834A (en) | 1957-04-01 | 1958-03-25 | Mixed anhydrides and their use as catalysts for the polymerisation of ethylenically unsaturated compounds |
| DEI14640A DE1104184B (de) | 1957-04-01 | 1958-03-31 | Polymerisation von aethylenisch ungesaettigten Verbindungen in Gegenwart von gemischten Anhydriden |
| FR1203746D FR1203746A (fr) | 1957-04-01 | 1958-04-01 | Anhydrides mixtes et leur application à titre de catalyseurs pour la polymérisation de composés éthyléniquement non-saturés |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB10532/57A GB826787A (en) | 1957-04-01 | 1957-04-01 | Mixed anhydrides and their use as catalysts for the polymerisation of ethylenically unsaturated compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB826787A true GB826787A (en) | 1960-01-20 |
Family
ID=9969566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB10532/57A Expired GB826787A (en) | 1957-04-01 | 1957-04-01 | Mixed anhydrides and their use as catalysts for the polymerisation of ethylenically unsaturated compounds |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2951834A (en:Method) |
| BE (1) | BE566277A (en:Method) |
| DE (1) | DE1104184B (en:Method) |
| FR (1) | FR1203746A (en:Method) |
| GB (1) | GB826787A (en:Method) |
| NL (1) | NL270779A (en:Method) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3322818A (en) * | 1963-03-04 | 1967-05-30 | Upjohn Co | New benzoylphenyl carbamates |
| FR2482587A1 (fr) * | 1980-05-14 | 1981-11-20 | Poudres & Explosifs Ste Nale | Procede de synthese de chloroformiates a-chlores et nouveaux chloroformiates a-chlores |
| US4460513A (en) * | 1982-10-25 | 1984-07-17 | Board Of Control Of Michigan Technological University | Method for preparing organic hyponitrites |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB618168A (en) * | 1946-10-30 | 1949-02-17 | Ian Marshall | Improvements in and relating to the polymerisation of compounds containing the ethylenic double bond |
| US2816883A (en) * | 1951-08-02 | 1957-12-17 | Du Pont | Product and process of polymerizing ethylene |
| CH356913A (de) * | 1954-06-08 | 1961-09-15 | Montedison Spa | Verfahren zur Polymerisation von olefinisch ungesättigten Kohlenwasserstoffen |
-
0
- NL NL270779D patent/NL270779A/xx unknown
- BE BE566277D patent/BE566277A/xx unknown
-
1957
- 1957-04-01 GB GB10532/57A patent/GB826787A/en not_active Expired
-
1958
- 1958-03-25 US US723645A patent/US2951834A/en not_active Expired - Lifetime
- 1958-03-31 DE DEI14640A patent/DE1104184B/de active Pending
- 1958-04-01 FR FR1203746D patent/FR1203746A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE566277A (en:Method) | |
| NL270779A (en:Method) | |
| FR1203746A (fr) | 1960-01-20 |
| US2951834A (en) | 1960-09-06 |
| DE1104184B (de) | 1961-04-06 |
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