GB1049091A - Catalyst suitable for use in polymerizing epoxy compounds - Google Patents
Catalyst suitable for use in polymerizing epoxy compoundsInfo
- Publication number
- GB1049091A GB1049091A GB2324463A GB2324463A GB1049091A GB 1049091 A GB1049091 A GB 1049091A GB 2324463 A GB2324463 A GB 2324463A GB 2324463 A GB2324463 A GB 2324463A GB 1049091 A GB1049091 A GB 1049091A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- catalyst
- group
- compounds
- valency
- 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
- 239000003054 catalyst Substances 0.000 title abstract 9
- 150000001875 compounds Chemical class 0.000 title abstract 8
- 239000004593 Epoxy Substances 0.000 title abstract 6
- 230000000379 polymerizing effect Effects 0.000 title 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 7
- -1 o-hydroxy-phenyl-carbonyl Chemical class 0.000 abstract 7
- 239000013522 chelant Substances 0.000 abstract 6
- 229910052751 metal Inorganic materials 0.000 abstract 5
- 239000002184 metal Substances 0.000 abstract 5
- 150000002902 organometallic compounds Chemical class 0.000 abstract 5
- 229910052723 transition metal Inorganic materials 0.000 abstract 5
- 150000003624 transition metals Chemical class 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 abstract 4
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical class C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 229910052720 vanadium Inorganic materials 0.000 abstract 3
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 abstract 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229910052804 chromium Inorganic materials 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 229910052742 iron Inorganic materials 0.000 abstract 2
- 229910052744 lithium Inorganic materials 0.000 abstract 2
- 229910052750 molybdenum Inorganic materials 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- SMQUZDBALVYZAC-UHFFFAOYSA-N ortho-hydroxybenzaldehyde Natural products OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 229910052719 titanium Inorganic materials 0.000 abstract 2
- ZWAJLVLEBYIOTI-OLQVQODUSA-N (1s,6r)-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCC[C@@H]2O[C@@H]21 ZWAJLVLEBYIOTI-OLQVQODUSA-N 0.000 abstract 1
- GELKGHVAFRCJNA-UHFFFAOYSA-N 2,2-Dimethyloxirane Chemical compound CC1(C)CO1 GELKGHVAFRCJNA-UHFFFAOYSA-N 0.000 abstract 1
- 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 1
- HRWYHCYGVIJOEC-UHFFFAOYSA-N 2-(octoxymethyl)oxirane Chemical compound CCCCCCCCOCC1CO1 HRWYHCYGVIJOEC-UHFFFAOYSA-N 0.000 abstract 1
- VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005725 8-Hydroxyquinoline Substances 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000732 arylene group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- ZGRWZUDBZZBJQB-UHFFFAOYSA-N benzenecarbodithioic acid Chemical compound SC(=S)C1=CC=CC=C1 ZGRWZUDBZZBJQB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000002738 chelating agent Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- UCAOGXRUJFKQAP-UHFFFAOYSA-N n,n-dimethyl-5-nitropyridin-2-amine Chemical compound CN(C)C1=CC=C([N+]([O-])=O)C=N1 UCAOGXRUJFKQAP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 210000000056 organ Anatomy 0.000 abstract 1
- 239000012430 organic reaction media Substances 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229960003540 oxyquinoline Drugs 0.000 abstract 1
- 150000005041 phenanthrolines Chemical class 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 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)
- Epoxy Resins (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Abstract
Epoxy compounds containing 2-20 carbon atoms are polymerized in the presence of a catalyst which comprises the product of reacting a metal chelate, other than an acetylacetonate, of the formula <FORM:1049091/C3/1> (wherein M is a transition metal from Group IV to VIII which may be attached to one or more oxygen atoms or lower alkoxy groups, D1 and D11, which may be the same or different, are oxygen, sulphur or nitrogen, R is an organic radical and p is an integer of at least 1 and is at most equal to the valency of M) with an organo metallic compound M1R1nXm (wherein M1\h is a metal of Groups I to III, R1 is a lower alkyl group, X is halogen, n is at least 1 and n + m equals the valency of M1), in an inert organic reaction medium under an atmosphere of an inert gas, the molar ratio of the metal chelate to the organo metallic compound being between 1:1 and 1:10. The preferred transition metals are Ti, V, Cr, Fe, Co, Ni, and Mo. Numerous chelating agents are specified, including b -keto-acid esters, b -diketones, o-hydroxy-phenyl-carbonyl compounds, b -keto-acid amides, aldehyde imines, oxy-azo compounds, aldoximes, dioximes, phenanthrolines, thiolactic acid, o-amino-benzene thiol and dithiobenzoic acid. The preferred organo-metallic compounds are LiR1, MgR12, ZnR12, AlR13, AlR12X and AlR1X2 where X and R1 are as above, e.g. butyl, lithium, diethyl zinc, triethyl aluminium, diethyl aluminium monochloride and ethyl-aluminium dichloride. The catalyst is normally prepared by heating the transition metal chelate and organometallic compound together in an inert diluent. Suitable epoxy compounds which may be polymerized or copolymerized are alkylene oxides, e.g. ethylene oxide, propylene oxide and isobutylene oxide, arylene oxides, e.g. styrene oxide, halogenated alkylene oxides, e.g. epichlorhydrin and b -methyl epichlorhydrin, diene monoepoxides, e.g. butadiene monoxide, saturated and unsaturated glycidyl ethers, e.g. allyl glycidyl ether and octyl glycidyl ether, alicyclic epoxides, e.g. cyclohexane oxide and phenyl glycidyl ethers which may be substituted in the phenyl group by H, halogen, a nitro group or a lower alkyl or aryl group. Usually the catalyst is used in an amount corresponding to 0.2-10 mol per cent of transition metal chelate based on the epoxy compound. Example I describes the preparation of a catalyst from triethylaluminium and (a) bis-(salicylaldehyde imine) cobalt (II) and (b) bis-(dimethyl-glyoxime) nickel (II). In Examples 2-37 epoxy compounds of the types exemplified above are polymerized alone using as catalysts complex compounds prepared from triethyl aluminium and bis-(dibenzoyl methane) Co (II), bis-(salicylaldehyde) Co (II), bis-(salicylaldehyde imine) Co (II), bis-(dimethyl-glyoxime) Ni (II), bis-(salicylaldehyde)-oxy vanadium, tris-(dimethyl glyoxime) Co (III), bis-(salicylaldoxime) Ni (II), bis-(cyclohexane dionedioxime) Ni (II), bis-(a -benzyl dioxime) Ni (II), and bis-(8-hydroxyquinoline) Co (II). In Examples 36-38 phenyl glycidyl ether and epichlorhydrin are copolymerized in the presence of AlEt3/bis-(dimethyl glyoxime) Ni (II) catalyst. The polymers and copolymers are used to form crystalline films and fibres. Those derived from phenyl glycidyl ether may be vulcanized or cross-linked.ALSO:The invention comprises a catalyst which is the reaction product of a metal chelate, other than an acetyl acetonate, <FORM:1049091/B1-B2/1> wherein M is a transition metal of Group IV to VIII and which may be attached to 1 or more O atoms of lower alkoxy groups, D1 and D11 are the same or different and are O, N or S, R is an organic radical and f is at least 1 and at most equals the valency of M, with an organo metallic compound M1Rn1 x m, wherein M1 is a metal of Group I to III, R1 is a lower alkyl group, X is halogen and n is at least and n + m equals the valency of M1, the chelate and the organs metallic compounds being reacted in an inert organic medium under an inert atmosphere and in the molar ratio 1:1 to 1:10. The terms 'lower alkyl' and 'lower alkoxy' are defined as groups having 1-4 carbon atoms. Specified values of M and Ti, V, Cr, Fe, Co, Ni and Mo, and of M1, Li, Mg, Zn and Al. A large number of chelating ligands-D1-R-D11-are specified. The catalysts are used in the polymerization of epoxy compounds to give polyethers.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3159862 | 1962-06-16 | ||
| JP3036963 | 1963-05-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1049091A true GB1049091A (en) | 1966-11-23 |
Family
ID=26368701
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2324463A Expired GB1049091A (en) | 1962-06-16 | 1963-06-11 | Catalyst suitable for use in polymerizing epoxy compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1049091A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997049713A1 (en) * | 1996-06-27 | 1997-12-31 | Union Carbide Chemicals & Plastics Technology Corporation | Catalyst for the production of olefin polymers |
-
1963
- 1963-06-11 GB GB2324463A patent/GB1049091A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997049713A1 (en) * | 1996-06-27 | 1997-12-31 | Union Carbide Chemicals & Plastics Technology Corporation | Catalyst for the production of olefin polymers |
| US5852146A (en) * | 1996-06-27 | 1998-12-22 | Union Carbide Chemicals & Plastics Technology Corporation | Catalyst for the production of olefin polymers |
| US6093824A (en) * | 1996-06-27 | 2000-07-25 | Univation Technologies, Llc | Catalyst for the production of olefin polymers |
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