1973
DOI: 10.1016/0032-3950(73)90211-6
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Some features of the synthesis of heat-resistant heterocyclic polymers

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Cited by 26 publications
(6 citation statements)
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“…The first important point to note is that the reactants and the product are in equilibrium, i.e. the propagation reaction is reversible [12,13]. The forward reaction is thought to start with the formation of a charge transfer complex between the dianhydride and the diamine [9,14,15].…”
Section: Two-step Methods For Polyimide Synthesismentioning
confidence: 99%
“…The first important point to note is that the reactants and the product are in equilibrium, i.e. the propagation reaction is reversible [12,13]. The forward reaction is thought to start with the formation of a charge transfer complex between the dianhydride and the diamine [9,14,15].…”
Section: Two-step Methods For Polyimide Synthesismentioning
confidence: 99%
“…At elevated temperatures, the conversion of amic acid to imide bonds is reversible. 45 Under vacuum, poly(amic acid) can thermally decompose into amine, carboxylic acid, and anhydride monomers. PIs may further react with other amine-containing compounds to deimidise and form crosslinking networks.…”
Section: Intramolecular Imidisationmentioning
confidence: 99%
“…Although PIs are durable under harsh chemical environment, the imide bond is still susceptible to degradation. At elevated temperatures, the conversion of amic acid to imide bonds is reversible 45 . Under vacuum, poly(amic acid) can thermally decompose into amine, carboxylic acid, and anhydride monomers.…”
Section: Syntheses Of Polyimidesmentioning
confidence: 99%
“…THF, not being very basic, does not associate with the polyamic acid and some reversal occurs. This "retro" reaction (k 2 ) occurs when a proton is transferred from a carboxylic acid to an amide nitrogen (or any other basic species), followed by the subsequent attack of the carboxylate oxygen on the adjacent carbonyl carbon to re-form the anhydride or the rare isoimide (25,27). This reverse reaction can be prevented by replacing the hydroxyl proton of the polyamic acid with amine salts or esters, causing a marked decrease in conversion to monomeric species (28)(29)(30).…”
Section: Reactionmentioning
confidence: 99%