GB1122925A - Nitrogen-containing polycondensates - Google Patents
Nitrogen-containing polycondensatesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular 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
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/20—Pyrrones
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.
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)
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 |
-
1966
- 1966-06-30 AT AT626566A patent/AT285766B/en not_active IP Right Cessation
- 1966-09-09 GB GB4043966A patent/GB1122925A/en not_active Expired
Cited By (2)
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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