Abstract
A detailed comparative study of polypyromellitamido acids and polyimides based on 2,5-bis(paminophenyl)pyrimidine and 4,4′-diaminoterphenyl was conducted to determine the role of the nitrogencontaining pyrimidine ring in the main chain of the polymers. A model of the layer packing of polyimide chains in crystalline regions was proposed based on the data from x-ray structural analysis and quantum chemical calculations. The existence of tilted packing caused by partial displacement of the solvent molecules bound to the pyrimidine ring of the neighboring macromolecule with higher basicity in pyrimidine-containing polymers was hypothesized.
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Additional information
Institute of Macromolecular Compounds, Russian Academy of Sciences, 199004 Saint Petersburg. Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, 630090 Novosibirsk. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 10, pp. 2288–2296, October, 1992.
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Artem'eva, V.N., Kudryavtsev, V.V., Nekrasova, E.M. et al. Investigation of the role of the pyrimidine ring in the main chain of polyamido acids and polyimides. 1. Supermolecular structure of polypyromellitimides based on 2,5-bis(p-aminophenyl)pyrimidine and its carbocyclic analog 4,4′-diaminoterphenyl. Russ Chem Bull 41, 1790–1796 (1992). https://doi.org/10.1007/BF00863810
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DOI: https://doi.org/10.1007/BF00863810