Soft x-ray diffraction of striated muscle
S.F. Fan, W.B. Yun, et al.
Proceedings of SPIE 1989
We report here the synthesis and characterization of poly(amic ethyl ester) oligomers functionalized with trimethoxysilyl end-groups. The oligomers were prepared via the condensation of 1,1-bis(4-aminophenyl)-1-phenyl-2,2,2-trifluoroethane, diethyldichloromellitate and p-aminophenyltrimethoxysilane. The p-aminophenyltrimethoxysilane was used to control both molecular weight and end-group functionality. These oligomers were thermally cured to form crosslinked networks. The resulting networks possessed Tg in excess of 450°C and thermal decomposition temperatures in the proximity of 500°C. The formation of networks was confirmed by swelling studies. These oligomers offer an attractive processing alternative as low viscosity precursors to crosslinked polyimide networks. © 1997 Elsevier Science Ltd.
S.F. Fan, W.B. Yun, et al.
Proceedings of SPIE 1989
Frank R. Libsch, Takatoshi Tsujimura
Active Matrix Liquid Crystal Displays Technology and Applications 1997
Kigook Song, Robert D. Miller, et al.
Macromolecules
Revanth Kodoru, Atanu Saha, et al.
arXiv