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GB1049091A - Catalyst suitable for use in polymerizing epoxy compounds - Google Patents

Catalyst suitable for use in polymerizing epoxy compounds

Info

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
Application number
GB2324463A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsui Chemical Industry Co Ltd
Original Assignee
Mitsui Chemical Industry Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsui Chemical Industry Co Ltd filed Critical Mitsui Chemical Industry Co Ltd
Publication of GB1049091A publication Critical patent/GB1049091A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/04Macromolecular 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
    • C08G65/06Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
    • C08G65/08Saturated oxiranes
    • C08G65/10Saturated oxiranes characterised by the catalysts used
    • C08G65/12Saturated 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.
GB2324463A 1962-06-16 1963-06-11 Catalyst suitable for use in polymerizing epoxy compounds Expired GB1049091A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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