Imide oligomers and co-oligomers containing pendent phenylethyny

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From carboxylic acid or derivative thereof

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528125, 528128, 528170, 528171, 528172, 528173, 528174, 528175, 528176, 528183, 528185, 528188, 528220, 528229, 528350, 524600, 524607, 526262, 526285, 526935, 4284111, 4284735, C08G 7310, C08G 6926

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056060149

ABSTRACT:
Controlled molecular weight imide oligomers and co-oligomers containing pendent phenylethynyl groups (PEPIs) and endcapped with nonreactive or phenylethynyl groups have been prepared by the cyclodehydration of the precursor amide acid oligomers or co-oligomers containing pendent phenylethynyl groups and endcapped with nonreactive or phenylethynyl groups. The amine terminated amide acid oligomers or co-oligomers are prepared from the reaction of dianhydride(s) with an excess of diamine(s) and diamine containing pendent phenylethynyl groups and subsequently endcapped with a phenylethynyl phthalic anhydride or monofunctional anhydride. The anhydride terminated amide acid oligomers and co-oligomers are prepared from the reaction of diamine(s) and diamine containing pendent phenylethynyl group(s) with an excess of dianhydride(s) and subsequently endcapped with a phenylethynyl amine or monofunctional amine. The polymerizations are carried out in polar aprotic solvents such as under nitrogen at room temperature. The amide acid oligomers or co-oligomers are subsequently cyclodehydrated to the corresponding imide oligomers. The polymers and copolymers prepared from these materials exhibit a unique and unexpected combination of properties.

REFERENCES:
patent: 4837300 (1989-06-01), St. Clair et al.
patent: 5138028 (1992-08-01), Paul et al.
Polymer Preprints, vol. 30, No. 1 (Apr. 1989), "Model Branched Poly(methylmethacrylates of Controlled Molecular Weight and Architecture; Synthesis Characterization", Siochi et al, pp. 141-143, 137-140.

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