PERFLUORO COMPOUNDS
1390672 Phosphorus-containing perfluoroalkyl derivatives CIBA-GEIGY AG 24 Feb 1972 [25 Feb 1971 29 Dec 1971] 8653/72 Headings C2P and C2C [Also in Division D1] Perfluoralkyl compounds containing phosphorus are obtained by reacting a perfluoroalkylalkene with a phosphorus trihalide with exclusion of...
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23.08.1973
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Abstract | 1390672 Phosphorus-containing perfluoroalkyl derivatives CIBA-GEIGY AG 24 Feb 1972 [25 Feb 1971 29 Dec 1971] 8653/72 Headings C2P and C2C [Also in Division D1] Perfluoralkyl compounds containing phosphorus are obtained by reacting a perfluoroalkylalkene with a phosphorus trihalide with exclusion of moisture and in the presence of oxygen or an oxygen-containing gas. Specified phosphorus trihalides are PC1 3 , PBr 3 and PI 3 and when the former is used for reaction with a perfluoroalkene of the formula where R 2 and R 3 each denote H or an unbranched or branched hydrocarbon radical and R is a C 1 -C 22 perfluoroalkyl radical (which is defined as an alkyl radical in which all the H atoms are replaced by F or all except a terminal (#) hydrogen atom are replaced by F) the products have the general formula wherein R denotes a perfluoroalkyl radical with 1 to 22 carbon atoms, A denotes a radical of the formula wherein R is bonded to the carbon atom (1) or (2), for each -(O) n-1 POCl 2 radical n is 1 or 2 with the proviso that in the case of formula (3) for n = 1a-(O) n-1 POOl 2 radical is bonded to at least one of R 2 and R 3 and for n = 2 to carbon atom (1) and, optionally, to at least one of R 2 and R 3 , and in the case of formula (4) for n = 1 or 2 a -(O) n-1 POCl 2 radical is bonded to at least one of R 2 11 and R 3 11 ; R 2 and R 3 each denote a hydrogen atom or an unbranched or branched hydrocarbon radical or a radical derived from an unbranched or branched hydrocarbon radical obtained by splitting off hydrogen atoms, to provide for R 2 and R 3 together up to 7 sites for the phosphorus-containing radicals, R11 2 is as defined under R 2 , and R 2 , R 3 and R 2 11 are not hydrogen when a phosphoruscontaining radical is bonded thereto, R11 3 denotes a radical derived from an unbranched or branched hydrocarbon radical by splitting off hydrogen atoms to provide for R11 2 and R113 together 1 to 8 sites for the phosphorus-containing radicals. The invention also includes as novel products those compounds having the above formula wherein R is a perfluoroalkyl radical (as defined above) containing 4 to 14 carbon atoms, R 2 R11 2 and R 3 are as defined above but when they are hydrocarbon radicals contain 1 to 18 carbon atoms, and R113 is as defined above but is derived from an alkyl radical having 1 to 18 carbon atoms and r is 1 to 8. The molar ratio of the phosphorus trihalide to the perfluoroalkene is generally from 2 : 1 to 20 : 1 preferably 2 : 1 to 10 : 1, and the reaction may be carried out in an inert solvent. The products are useful for the production of oleophobic finishes on porous and non-porous substances, e.g. leather, paper, textile materials, metals, plastics and glass. A perfluoroheptylbutene isomer mixture is obtained by addition of perfluoroheptyl iodide to isobutylene and alkaline elimination of HI. A perfluoroheptyl octene isomer is obtained analogously using n-octene-(1). |
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AbstractList | 1390672 Phosphorus-containing perfluoroalkyl derivatives CIBA-GEIGY AG 24 Feb 1972 [25 Feb 1971 29 Dec 1971] 8653/72 Headings C2P and C2C [Also in Division D1] Perfluoralkyl compounds containing phosphorus are obtained by reacting a perfluoroalkylalkene with a phosphorus trihalide with exclusion of moisture and in the presence of oxygen or an oxygen-containing gas. Specified phosphorus trihalides are PC1 3 , PBr 3 and PI 3 and when the former is used for reaction with a perfluoroalkene of the formula where R 2 and R 3 each denote H or an unbranched or branched hydrocarbon radical and R is a C 1 -C 22 perfluoroalkyl radical (which is defined as an alkyl radical in which all the H atoms are replaced by F or all except a terminal (#) hydrogen atom are replaced by F) the products have the general formula wherein R denotes a perfluoroalkyl radical with 1 to 22 carbon atoms, A denotes a radical of the formula wherein R is bonded to the carbon atom (1) or (2), for each -(O) n-1 POCl 2 radical n is 1 or 2 with the proviso that in the case of formula (3) for n = 1a-(O) n-1 POOl 2 radical is bonded to at least one of R 2 and R 3 and for n = 2 to carbon atom (1) and, optionally, to at least one of R 2 and R 3 , and in the case of formula (4) for n = 1 or 2 a -(O) n-1 POCl 2 radical is bonded to at least one of R 2 11 and R 3 11 ; R 2 and R 3 each denote a hydrogen atom or an unbranched or branched hydrocarbon radical or a radical derived from an unbranched or branched hydrocarbon radical obtained by splitting off hydrogen atoms, to provide for R 2 and R 3 together up to 7 sites for the phosphorus-containing radicals, R11 2 is as defined under R 2 , and R 2 , R 3 and R 2 11 are not hydrogen when a phosphoruscontaining radical is bonded thereto, R11 3 denotes a radical derived from an unbranched or branched hydrocarbon radical by splitting off hydrogen atoms to provide for R11 2 and R113 together 1 to 8 sites for the phosphorus-containing radicals. The invention also includes as novel products those compounds having the above formula wherein R is a perfluoroalkyl radical (as defined above) containing 4 to 14 carbon atoms, R 2 R11 2 and R 3 are as defined above but when they are hydrocarbon radicals contain 1 to 18 carbon atoms, and R113 is as defined above but is derived from an alkyl radical having 1 to 18 carbon atoms and r is 1 to 8. The molar ratio of the phosphorus trihalide to the perfluoroalkene is generally from 2 : 1 to 20 : 1 preferably 2 : 1 to 10 : 1, and the reaction may be carried out in an inert solvent. The products are useful for the production of oleophobic finishes on porous and non-porous substances, e.g. leather, paper, textile materials, metals, plastics and glass. A perfluoroheptylbutene isomer mixture is obtained by addition of perfluoroheptyl iodide to isobutylene and alkaline elimination of HI. A perfluoroheptyl octene isomer is obtained analogously using n-octene-(1). |
Author | HELMUT HUBER-EMDEN |
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SubjectTerms | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR LAUNDERING METALLURGY ORGANIC CHEMISTRY TEXTILES TREATMENT OF TEXTILES OR THE LIKE TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS,FABRICS, FEATHERS, OR FIBROUS GOODS MADE FROM SUCH MATERIALS |
Title | PERFLUORO COMPOUNDS |
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