GB1082104A - Polyepoxides - Google Patents

Polyepoxides

Info

Publication number
GB1082104A
GB1082104A GB4060565A GB4060565A GB1082104A GB 1082104 A GB1082104 A GB 1082104A GB 4060565 A GB4060565 A GB 4060565A GB 4060565 A GB4060565 A GB 4060565A GB 1082104 A GB1082104 A GB 1082104A
Authority
GB
United Kingdom
Prior art keywords
alkyl
hydrocarbon
aryl
carbon atoms
halogen
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
GB4060565A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB4060565A priority Critical patent/GB1082104A/en
Publication of GB1082104A publication Critical patent/GB1082104A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/22Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/16Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by esterified hydroxyl radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/34Compounds containing oxirane rings with hydrocarbon radicals, substituted by sulphur, selenium or tellurium atoms
    • 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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22Di-epoxy compounds
    • C08G59/30Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen
    • C08G59/302Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen containing sulfur

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Epoxy resins are prepared by treating an epoxide coupling reagent and, optionally, an epoxide polymerizing catalyst with novel polythioepoxides, preferably of formula <FORM:1082104/C3/1> where n is an integer of 2 or more; R is an n-valent organic radical, such that at least 2 of the sulphur atoms are no more than 6 carbon atoms away from each other or from a negative activating group; R is a hydrocarbon, hydrocarbon-ether or hydrocarbon-ester chain including at least 2 carbon atoms, which hydrocarbon chain may comprise a 5- or 6-membered carbocyclic ring, or an alkyl, aryl or halogen substituted derivative thereof; R2 and R3 are hydrogen, alkyl or halogen; R4, when not connected to R1, is hydrogen, halogen, alkyl, haloalkyl, aryl, haloaryl, alkyaryl or haloalkaryl, and, when connected to R1, is a hydrocarbon chain of 2 or 3 carbon atoms or an alkyl, aryl or halogen substituted derivative thereof, are prepared by reacting a polymercaptan R(SH)n with an olefinically unsaturated epoxide containing at least one vicinal epoxide group separated from an olefin group by at least one carbon, the olefin group being located in a 5 or 6-membered carbon ring or in a terminal position in an aliphatic hydrocarbon chain, the reaction product not containing the radical -S-CH2-S-. Specified negative activating groups are -C(O)O-, -OH, -S-, -O- and -CO-. Examples prepare resins from reaction products of 1,4-butanedithiol and various esters of polyhydric compounds with mercaptoacetic and b -mercaptopropionic acids with alkyl glycidyl ether, the glycidyl ether of 2-alkyl-phenol, vinyl-3,4-epoxycyclohexane, limonene monoxide or glycidyl acrylate. The polythioepoxides may be prepared, at least in part, in situ in the presence of the epoxide coupling agent. Examples use methylbicyclo-2,2,1-hept-5-ene-2,3-dicarboxylic anhydride, phthalic anhydride or maleic anhydride as coupling agents, and 2,4,6-tris(dimethylaminomethyl)phenol as catalyst, when used. The mercaptoacetate of an allyl alcohol-styrene copolymer is prepared in Example 8 by conventional esterification and the mercaptoacetate of a phenol-formaldehyde resin similarly in Example 14. The novel polythioepoxides described above may be used to stabilize vinyl chloride resin compositions.ALSO:Novel polythio - group containing polyepoxides, preferably of formula <FORM:1082104/C2/1> where n is an integer of 2 or more; R is an n-valent organic radical, such that at least 2 of the sulphur atoms are no more than 6 carbon atoms away from each other or from a negative activating group; R1 is a hydrocarbon, hydrocarbon-ether or hydrocarbon-ester chain including at least 2 carbon atoms, which hydrocarbon chain may comprise a 5- or 6-membered carbocyclic ring, or an alkyl, aryl or halogen substituted derivative thereof; R2 and R3 are hydrogen, alkyl or halogen; R4, when not connected to R1 is hydrogen, halogen, alkyl, haloalkyl, aryl, haloaryl, alkaryl or haloalkaryl, and, when connected to R1 is a hydrocarbon chain of 2 or 3 carbon atoms or an alkyl, aryl or halogen substituted derivative thereof, are prepared by reacting a polymercaptan R(SH)n with an olefinically unsaturated epoxide containing at least one vicinal epoxide group separated from an olefin group by at least one carbon, the olefin group being located in a 5- or 6-membered carbon ring or in a terminal position in an aliphatic hydrocarbon chain, the reaction product not containing the radical -S-CH2-S-. Specified negative activating groups are -C(O)O-, -OH, -S-, -O-and -CO-. Examples react 1,4-butanedithiol and various esters of polyhydric compounds with mercaptoacetic and b -mercaptopropionic acids with allyl glycidyl ether, the glycidyl ether of 2-allylphenol, vinyl-3,4-epoxycyclohexane, limonene monoxide, or glycidyl acrylate. Conventional esterification is used to prepare, as starting materials, the completely esterified mercaptoacetate of triethylene glycol, 1,4 - butanediol, 1,1,1 - trimethylolpropane, glycerol, 1,1,1 - trimethylolethane, pentaery - thritol, hydroxylated castor oil and bisphenol A, the b - mercaptopropionate of 1,1,1 - trimethylolpropane, mixed esters of pentaerythritol with mercaptoacetic acid and soya bean oil acids and of 1,1,1-trimethylolpropane with mercaptoacetic and dimerized soya bean oil acids, and the mercaptoethanol ester of adipic acid.
GB4060565A 1965-09-23 1965-09-23 Polyepoxides Expired GB1082104A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4060565A GB1082104A (en) 1965-09-23 1965-09-23 Polyepoxides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4060565A GB1082104A (en) 1965-09-23 1965-09-23 Polyepoxides

Publications (1)

Publication Number Publication Date
GB1082104A true GB1082104A (en) 1967-09-06

Family

ID=10415719

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4060565A Expired GB1082104A (en) 1965-09-23 1965-09-23 Polyepoxides

Country Status (1)

Country Link
GB (1) GB1082104A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120071587A1 (en) * 2009-03-16 2012-03-22 Astrium Sas Use of curable resins containing a prepolymer based on glycidyl (meth)acrylate for making materials for use in space
CN104262624A (en) * 2014-09-03 2015-01-07 浙江大学 Synthetic method of polyepoxy polymer
WO2018049302A1 (en) * 2016-09-12 2018-03-15 Poly6 Technologies One-pot, high-performance recycling method for polymer waste using renewable polymer synthesis
CN112794991A (en) * 2021-02-01 2021-05-14 南宁珀源能源材料有限公司 Acrylic acid modified polythiol curing agent and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120071587A1 (en) * 2009-03-16 2012-03-22 Astrium Sas Use of curable resins containing a prepolymer based on glycidyl (meth)acrylate for making materials for use in space
CN104262624A (en) * 2014-09-03 2015-01-07 浙江大学 Synthetic method of polyepoxy polymer
WO2018049302A1 (en) * 2016-09-12 2018-03-15 Poly6 Technologies One-pot, high-performance recycling method for polymer waste using renewable polymer synthesis
CN112794991A (en) * 2021-02-01 2021-05-14 南宁珀源能源材料有限公司 Acrylic acid modified polythiol curing agent and preparation method thereof

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