GB1122925A - Nitrogen-containing polycondensates - Google Patents

Nitrogen-containing polycondensates

Info

Publication number
GB1122925A
GB1122925A GB4043966A GB4043966A GB1122925A GB 1122925 A GB1122925 A GB 1122925A GB 4043966 A GB4043966 A GB 4043966A GB 4043966 A GB4043966 A GB 4043966A GB 1122925 A GB1122925 A GB 1122925A
Authority
GB
United Kingdom
Prior art keywords
benzoic acid
groups
acid
residues
benzimidazol
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
GB4043966A
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.)
Axalta Coating Systems Germany GmbH and Co KG
Original Assignee
Herberts GmbH
Dr Kurt Herberts and Co GmbH
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 Herberts GmbH, Dr Kurt Herberts and Co GmbH filed Critical Herberts GmbH
Publication of GB1122925A publication Critical patent/GB1122925A/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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/20Pyrrones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Insulating Materials (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

The invention comprises branched polycondensates which contain (a) residues of compounds containing both 2 and more than 2 functional groups which are amino, hydroxyl and/or carboxyl groups, the residues being joined by ester, amide, imide, benzimidazole and/or benzoxazole group and (b) 2-(benzimidazol-21yl) benzoic acid residues or 2-(benzimidazol-21yl) benzoic acid lactam residues, joined to the remainder of the molecule through their 3, 4, 5 or 6 and 41, 51, 61 or 71 positions, by another such residue or one of the above linking groups. Compounds containing the 2-(benzimidazol-21yl) benzoic acid or acid lactam residue may be derived from (i) an aromatic compound containing 2 mutually ortho carboxyl groups and at least one other functional group and (ii) an aromatic compound having 2 mutually ortho amino-groups and at least one other functional group. This reaction may be at 100-300 DEG C. in a solvent, the reactants being added to the reaction vessel alternately or mixed and added in portions, the portions being of the same or differing reactant ratios. These compounds may be polycondensed with other reactants such as polycarboxylic acids, polyamines, polyhydric alcohols, polyhydric phenols, aminoacids, hydroxyacids, aminoalcohols, and aminophenols at up to 300 DEG C. in an inert gas flow. The polycondensates may be dissolved in organic solvents containing hardening agents, applied to conductors and heated at 150-650 DEG C. to cure them to an insulating coating. In examples, 2-(benzimidazoyl) benzoic acid and acid lactam forming compounds used are trimellitic anhydride, 3,4-diamino benzoic acid and 3,31-diaminobenzidene. Other reactants are a polyester prepared from ethylene glycol, glycerol and terephthalic acid in the presence of zinc acetate, trimellitic anhydride, diamino diphenyl methane, diphenyl terephthalate, a polyester prepared from ethylene glycol, glycerol, terephthalic acid and naphthalene-2,6-dicarboxylic acid in the presence of zinc acetate, 3,4-diamino-benzoic acid and methyl phenyl terephthalate. The products are dissolved in cresol and transesterified with butyl titanate to introduce titanate groups into them. The treated solution is diluted with a mixture of cresol, naphtha, xylene, tetralin and pine-base levelling agent to form a wire lacquer.
GB4043966A 1965-09-09 1966-09-09 Nitrogen-containing polycondensates Expired GB1122925A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEH0057122 1965-09-09
DEH0057123 1965-09-09

Publications (1)

Publication Number Publication Date
GB1122925A true GB1122925A (en) 1968-08-07

Family

ID=25980352

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4043966A Expired GB1122925A (en) 1965-09-09 1966-09-09 Nitrogen-containing polycondensates

Country Status (2)

Country Link
AT (1) AT285766B (en)
GB (1) GB1122925A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1979001029A1 (en) * 1978-05-03 1979-11-29 Us Commerce Aromatic heterocyclic polymer alloys and products produced therefrom

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1979001029A1 (en) * 1978-05-03 1979-11-29 Us Commerce Aromatic heterocyclic polymer alloys and products produced therefrom
US4207407A (en) * 1978-05-03 1980-06-10 The United States Of America As Represented By The Secretary Of The Air Force Aromatic heterocyclic polymer alloys and products produced therefrom

Also Published As

Publication number Publication date
AT285766B (en) 1970-11-10

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