GB1224774A - Novel compounds containing fluoroisoalkoxyalkyl radicals - Google Patents
Novel compounds containing fluoroisoalkoxyalkyl radicalsInfo
- Publication number
- GB1224774A GB1224774A GB09754/68A GB1975468A GB1224774A GB 1224774 A GB1224774 A GB 1224774A GB 09754/68 A GB09754/68 A GB 09754/68A GB 1975468 A GB1975468 A GB 1975468A GB 1224774 A GB1224774 A GB 1224774A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fluorine
- vinyl
- chlorine
- radical
- april
- 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
- 150000001875 compounds Chemical class 0.000 title 1
- -1 alkylene radical Chemical class 0.000 abstract 6
- 229910052731 fluorine Inorganic materials 0.000 abstract 5
- 239000011737 fluorine Substances 0.000 abstract 5
- 229910052801 chlorine Chemical group 0.000 abstract 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 3
- 239000000460 chlorine Chemical group 0.000 abstract 3
- 239000005977 Ethylene Substances 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Chemical group 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 125000006545 (C1-C9) alkyl group Chemical group 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 238000012662 bulk polymerization Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 239000003431 cross linking reagent Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 238000007720 emulsion polymerization reaction Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000010557 suspension polymerization reaction Methods 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
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- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- Textile Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
1,224,774. Polymers of fluorine-containing (meth)acrylates. ALLIED CHEMICAL CORP. 25 April, 1968 [25 April, 1967 (2); 12 April, 1968 (2)], No. 19754/68. Heading C3P. [Also in Divisions B2, C2 and D1] Polymers comprising recurring units of the formula useful as impregnating and coating agents, are obtained by polymerizing acrylates or methacrylates of the formula wherein each R 1 radical is independently a fluorine or chlorine atom or a C 1-9 alkyl group, which is optionally substituted by fluorine, chlorine or bromine, or two R 1 radicals form a C 1-18 alkylene radical, which is optionally substituted by chlorine, bromine or fluorine; A is a radical -CFR 3 -R 4 R 5 -, R 3 and R 4 being independently hydrogen or fluorine atoms and R 5 being a hydrogen, fluorine, chlorine or bromine atom; C and D are each independently ethylene radicals or certain substituted ethylene radicals provided that L is joined to a methylene group; m is from 0 to 75; n is from 0 to 75; v is 0 or 1; and L is a OCOC(M)=CH 2 group, M being a hydrogen atom or a methyl group. The polymerization may be effected by solution, bulk, emulsion or suspension polymerization and in the presence of free-radical generating catalysts, e.g. peroxides, chain-transfer agents, cross-linking agents, water-soluble organic solvents and/or inorganic salts. Co-monomers may also be used, e.g. vinyl esters, vinyl halides, vinyl alkyl ketones, vinyl alkyl sulphones, vinyl ethers, N-vinyl pyrrolidone, aliphatic and aromatic olefins, other acrylic compounds, and other unsaturated acid esters. Numerous examples are given, The alcohol is used in an example as solvent for the solution polymerization of the methacrylate monomer (CF 3 ) 2 CF-O-CF 2 CF 2 -CH 2 CH 2 -OCO-C(CH 3 )=CH 2 in the presence of α,α<SP>1</SP>- azobisisobutyronitrile.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US63336867A | 1967-04-25 | 1967-04-25 | |
US63335967A | 1967-04-25 | 1967-04-25 | |
US72108968A | 1968-04-12 | 1968-04-12 | |
US72111468A | 1968-04-12 | 1968-04-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1224774A true GB1224774A (en) | 1971-03-10 |
Family
ID=27505202
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB09754/68A Expired GB1224774A (en) | 1967-04-25 | 1968-04-25 | Novel compounds containing fluoroisoalkoxyalkyl radicals |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE714161A (en) |
DE (1) | DE1770262A1 (en) |
FR (1) | FR1580225A (en) |
GB (1) | GB1224774A (en) |
IL (1) | IL29893A0 (en) |
NL (1) | NL6805862A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998012163A1 (en) * | 1996-09-18 | 1998-03-26 | Exfluor Research Corporation | Method for preparing perfluorocarbon-substituted methanols |
US10954323B2 (en) | 2016-06-17 | 2021-03-23 | Merck Patent Gmbh | Fluorine containing polymers |
-
1968
- 1968-04-24 BE BE714161D patent/BE714161A/xx unknown
- 1968-04-25 DE DE19681770262 patent/DE1770262A1/en active Pending
- 1968-04-25 FR FR149517A patent/FR1580225A/fr not_active Expired
- 1968-04-25 GB GB09754/68A patent/GB1224774A/en not_active Expired
- 1968-04-25 IL IL29893A patent/IL29893A0/en unknown
- 1968-04-25 NL NL6805862A patent/NL6805862A/xx unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998012163A1 (en) * | 1996-09-18 | 1998-03-26 | Exfluor Research Corporation | Method for preparing perfluorocarbon-substituted methanols |
US6479712B1 (en) | 1996-09-18 | 2002-11-12 | Exfluor Research Corporation | Method for preparing perfluorocarbon-substituted methanols |
US10954323B2 (en) | 2016-06-17 | 2021-03-23 | Merck Patent Gmbh | Fluorine containing polymers |
Also Published As
Publication number | Publication date |
---|---|
IL29893A0 (en) | 1968-09-26 |
DE1770262A1 (en) | 1972-03-30 |
BE714161A (en) | 1968-09-16 |
NL6805862A (en) | 1968-10-28 |
FR1580225A (en) | 1969-09-05 |
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