GB897099A - Polymerization of acetylene compounds - Google Patents

Polymerization of acetylene compounds

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Publication number
GB897099A
GB897099A GB42078/60A GB4207860A GB897099A GB 897099 A GB897099 A GB 897099A GB 42078/60 A GB42078/60 A GB 42078/60A GB 4207860 A GB4207860 A GB 4207860A GB 897099 A GB897099 A GB 897099A
Authority
GB
United Kingdom
Prior art keywords
nickel
chloride
acetylene
osmium
metal
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
GB42078/60A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB897099A publication Critical patent/GB897099A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Polymerization Catalysts (AREA)

Abstract

Acetylene and monosubstituted acetylenes are polymerized and copolymerized by processes which comprise contacting the monomers under polymerization conditions with a catalyst composition comprising a mixture of (1) a simple or complex metal salt represented by the formula Mp NnXm wherein m is 1 to 6, n is 0 or 1 to 6, and when N is osmium m is 1 to 8, n is 0 or 1 to 8, p is 0 or 1 to 4 and wherein p and n cannot be zero at the same time; N is nickel, cobalt, palladium, platinum, rhodium, iridium, ruthenium or osmium; M is any metal of valency 1 to 4; and X is an anion of valency 1 to 6 and is a complex anion containing N when n is 0; and (2) a hydride of a Group I, II, III or IV element having at least one hydridic hydrogen and no metal-to-carbon bonds, or a metal hydride of another Group having at least one hydridic hydrogen and no metal-to-carbon bonds. The polymers obtained may be linear or aromatic and specified monomers are acetylene, propyne, butyne-1, heptyne-1, phenyl acetylene and propargyl alcohol, and mixtures of acetylene and propyne, acetylene and butyne-1, acetylene and heptyne-1, acetylene and phenyl acetylene, acetylene and propargyl alcohol, and pentyne-1 and heptyne-1. Many suitable catalyst components are specified, the use of the following being exemplified: sodium borohydride with cobalt nitrate, nickel chloride, cobalt chloride, nickel bromide, palladium chloride, potassium chloroplatinate, platinium chloride, nickel fluoride, cobalt fluoride, osmium chloride, nickel sulphate, nickel phosphate, nickel cyanide, nickel ferrocyanide, nickel ferricyanide, nickel thiocyanate, nickel acetate and nickel iodide; potassium borohydride with ruthenium chloride, rhodium chloride and iridium chloride; lithium borohydride with nickel chloride; lithium aluminium hydride with osmium chloride, nickel bromide and nickel chloride; lithium hydride with rhodium chloride, nickel chloride and nickel bromide; diborane with platinum chloride and nickel chloride; monosilane with palladium nitrate and NaBH(OCH3)3 with nickel chloride. Polymerization may be effected in the presence of solvents, e.g. water, ethanol, ethyl acetate, ethyl ether, dioxane, tetrahydrofuran, dimethyl formamide, acetonitrile, heptane and xylene, and mixture of acetonitrile with tetrahydrofuran and dioxane with ethanol. The products may be washed with benzene, hexane, petroleum ether, acetone, methanol, methanolic hydrochloric acid and water. The products may be used as drying oils and additives for varnishes, enamels and paints; pigments; ultra-violet light absorbers; antioxidants; intermediates for making polyalcohols, polymethoxides and methoxy resins; absorbants and fillers for rubber compositions.ALSO:Acetylene and monosubstituted acetylenes are polymerized or copolymerized to low molecular weight polymers or copolymers, e.g. containing two to twenty units, by processes which comprise contacting the monomers under polymerization conditions with a catalyst composition comprising a mixture of (1) a simple or complex metal salt represented by the formula MpNnXm wherein m is 1 to 6, n is 0 or 1 to 6, and when N is osmium m is 1 to 8, n is 0 or 1 to 8, p is 0 or 1 to 4 and wherein p and n cannot be zero at the same time; N is nickel, cobalt, palladium, platinum, rhodium, iridium, ruthenium or osmium; M is any metal having a valence of 1 to 4; and X is an anion of valence 1 to 6 and is a complex anion containing N when n is 0; and (2) a hydride of a Group I, II, III or IV element having at least one hydridic hydrogen and no metal-to-carbon bonds, or a metal hydride of another Group having at least one hydridic hydrogen and no metal-to-carbon bonds. The polymers obtained may be linear or aromatic and specified monomers are acetylene, propyne, butyne-1, heptyne-1, phenyl acetylene and propargyl alcohol, and mixtures of acetylene and propyne, acetylene and butyne-1, acetylene and heptyne-1, acetylene and phenyl acetylene, acetylene and propargyl alcohol, and pentyne-1 and heptyne-1. Examples describe the preparation of (28) linear dimers and trimers of heptyne-1 (34) aromatic polymers of propargyl alcohol and (49) linear and aromatic polymers of phenyl acetylene. Many suitable catalyst components are specified, and the use of the following exemplified: sodium borohydride with cobalt nitrate, cobalt chloride, cobalt fluoride, nickel chloride, nickel bromide, nickel fluoride, nickel sulphate, nickel phosphate, nickel cyanide, nickel ferrocyanide, nickel ferricyanide, nickel thiocyanate, nickel acetate, nickel iodide, palladium chloride, platinum chloride, potassium chloroplatinate and osmium chloride; potassium borohydride with ruthenium chloride, rhodium chloride and iridium chloride; lithium borohydride with nickel chloride; lithium aluminium hydride with osmium chloride, nickel bromide and nickel chloride; lithium hydride with rhodium chloride, nickel chloride and nickel bromide; diborane with platinum chloride and nickel chloride; monosilane with palladium nitrate; and NaBH(OCH3)3 with nickel chloride. Polymerization may be effected in the presence of solvents, e.g. water, ethanol, ethyl acetate, ethyl ether, dioxane, tetrahydrofuran, dimethyl formamide acetonitrile, heptane and xylene, and mixtures of acetonitrile with tetrahydrofuran, and dioxane with ethanol. The products may be used as drying oils and additives for varnishes, enamels and paints; ultraviolet light absorbers; antioxidants and intermediates for making polyalcohols, polymethoxides and methoxy resins.
GB42078/60A 1959-12-08 1960-12-07 Polymerization of acetylene compounds Expired GB897099A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US897099XA 1959-12-08 1959-12-08

Publications (1)

Publication Number Publication Date
GB897099A true GB897099A (en) 1962-05-23

Family

ID=22219194

Family Applications (1)

Application Number Title Priority Date Filing Date
GB42078/60A Expired GB897099A (en) 1959-12-08 1960-12-07 Polymerization of acetylene compounds

Country Status (1)

Country Link
GB (1) GB897099A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3336275A (en) * 1964-09-08 1967-08-15 Interchem Corp Process for the polymerization of norbornene derivatives using salts of iridium, osmium or ruthenium
US4359563A (en) * 1979-08-18 1982-11-16 Basf Aktiengesellschaft Preparation of acetylene copolymers
CN115463692A (en) * 2022-09-29 2022-12-13 南开大学 N-containing five-membered heterocyclic ligand modified ruthenium-based catalyst for acetylene hydrochlorination reaction and preparation method and application thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3336275A (en) * 1964-09-08 1967-08-15 Interchem Corp Process for the polymerization of norbornene derivatives using salts of iridium, osmium or ruthenium
US4359563A (en) * 1979-08-18 1982-11-16 Basf Aktiengesellschaft Preparation of acetylene copolymers
CN115463692A (en) * 2022-09-29 2022-12-13 南开大学 N-containing five-membered heterocyclic ligand modified ruthenium-based catalyst for acetylene hydrochlorination reaction and preparation method and application thereof
CN115463692B (en) * 2022-09-29 2023-10-10 南开大学 N-containing five-membered heterocyclic ligand modified ruthenium-based catalyst for hydrochlorination of acetylene as well as preparation method and application thereof

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