GB1060611A - The production of polymeric aromatic compounds from aromatic compounds having carbonyl halide or sulphonyl halide groups - Google Patents

The production of polymeric aromatic compounds from aromatic compounds having carbonyl halide or sulphonyl halide groups

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Publication number
GB1060611A
GB1060611A GB4101261A GB4101261A GB1060611A GB 1060611 A GB1060611 A GB 1060611A GB 4101261 A GB4101261 A GB 4101261A GB 4101261 A GB4101261 A GB 4101261A GB 1060611 A GB1060611 A GB 1060611A
Authority
GB
United Kingdom
Prior art keywords
halide
aromatic compounds
chloride
aromatic
polymeric
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
GB4101261A
Inventor
Alan Kutner
Michael James Stewart Dewar
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.)
SECR AVIATION
Minister of Aviation
Original Assignee
SECR AVIATION
Minister of Aviation
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 SECR AVIATION, Minister of Aviation filed Critical SECR AVIATION
Priority to GB4101261A priority Critical patent/GB1060611A/en
Publication of GB1060611A publication Critical patent/GB1060611A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B61/00Other general methods

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Abstract

Polymeric aromatic compounds are prepared by reacting an aromatic compound having two carbonyl halide or sulphonyl halide groups attached to the aromatic nucleus in relative positions other than ortho or meta, with an aromatic compound having two benzenoid nucleic on which are two replaceable hydrogen atoms at an elevated temperature in the presence of anhydrous hydrogen fluoride. The products are poly-ketones or sulphones resulting from the elimination of hydrogen halide. Specified acyl halide reactants are terephthalyl chloride, diphenylether - 4,41 - disulphonyl chloride, fluorene - 2,7 - disulphonyl chloride and naphthalene - 1,5 - disulphonyl chloride. Specified aromatic compounds are diphenyl ether, fluorene, bibenzthiophene, phenoxathiin, naphthalene and dibenzofuran. Normally the reactants are used in approximately equimolar proportions, preferably with a molar excess of hydrogen fluoride. Examples relate to polymeric compounds, containing up to 7 repeating units, which are stable up to 400 DEG C. and insoluble in a wide range of solvents.ALSO:Polymeric aromatic compounds are prepared by reacting an aromatic compound having two carbonyl halide or sulphonyl halide groups attached to the aromatic nucleus in relative positions other than ortho or meta, with an aromatic compound having two benzenoid nucleic on which are two replaceable hydrogen atoms at an elevated temperature in the presence of anhydrous hydrogen flouride. The products are poly-ketones or sulphones resulting from the elimination of hydrogen halide. Specified acyl halide reactants are terephthalyl chloride, diphenylether - 4,41 - disulphonyl chloride, fluorene - 2,7 - disulphonyl chloride and naphthalene 1,5-disulphonyl chloride. Specified aromatic compounds are diphenyl ether, fluorene, bibenzthiophene, phenoxathiin, naphthalene and dibensofuran. Normally, the reactants are used in approximately equimolar proportions, preferably with a molar excess of hydrogen flouride. Examples relate to polymeric compounds, containing up to 7 repeating units, which are stable up to 400 DEG C. and insoluble in a wide range of solvents.
GB4101261A 1961-11-16 1961-11-16 The production of polymeric aromatic compounds from aromatic compounds having carbonyl halide or sulphonyl halide groups Expired GB1060611A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4101261A GB1060611A (en) 1961-11-16 1961-11-16 The production of polymeric aromatic compounds from aromatic compounds having carbonyl halide or sulphonyl halide groups

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4101261A GB1060611A (en) 1961-11-16 1961-11-16 The production of polymeric aromatic compounds from aromatic compounds having carbonyl halide or sulphonyl halide groups

Publications (1)

Publication Number Publication Date
GB1060611A true GB1060611A (en) 1967-03-08

Family

ID=10417688

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4101261A Expired GB1060611A (en) 1961-11-16 1961-11-16 The production of polymeric aromatic compounds from aromatic compounds having carbonyl halide or sulphonyl halide groups

Country Status (1)

Country Link
GB (1) GB1060611A (en)

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