Oliver Schilter, Alain Vaucher, et al.
Digital Discovery
Imide-aryl ether thiophene copolymers were prepared and their thermal and mechanical properties were investigated. A key feature of these copolymers is the incorporation of the 2,5-thiophene moiety using 5,5′-bis[(3-aminophenoxy)thienyl-2] Ketone or 5,5′-bis[(4-aminophenoxy)thienyl-2] ketone as diamines in polyimide syntheses. The preparation of these thiophene diamines involved the nucleophilic aromatic substitution of bis(5-chlorothienyl-2) ketone with either 3- or 4-aminophenol in N-methyl-2-pyrrolidinone using potassium carbonate. These diamines were reacted with various compositions of pyromellitic dianhydride and 4,4′-oxydianiline to synthesize the desired poly(amic acid)s. Films were cast and cured (300°C) to effect the imide formation, and the resulting films showed tough ductile mechanical properties with high glass transition temperatures that decreased with increasing thiophene diamine content. © 1994.
Oliver Schilter, Alain Vaucher, et al.
Digital Discovery
Arvind Kumar, Jeffrey J. Welser, et al.
MRS Spring 2000
Kenneth R. Carter, Robert D. Miller, et al.
Macromolecules
E. Babich, J. Paraszczak, et al.
Microelectronic Engineering