In situ infrared spectroscopy study on imidization reaction and imidization-induced refractive index and thickness variations in microscale thin films of a poly(amic ester)

被引:38
作者
Shin, TJ [1 ]
机构
[1] Brookhaven Natl Lab, Natl Synchrotron Light Source Dept, Upton, NY 11973 USA
[2] Pohang Univ Sci & Technol, Polymer Res Inst, Ctr Integrated Mol Syst, Dept Chem, Pohang 790784, South Korea
[3] Pohang Univ Sci & Technol, Div Mol & Life Sci, Program BK21, Pohang 790784, South Korea
关键词
D O I
10.1021/la050470c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Poly(amic ester) (PAE) is a soluble precursor of polyimide that has attracted interest from both the microelectronic and the flat-panel display industries because of its several important advantages, including excellent solubility, high hydrolytic stability, and solvent-free film formation, over the polyimide precursor, poly(amic acid), for which monomer-polymer equilibration always occurs in solution due to its carboxylic acid groups. In this study, poly(3,4'-oxydiphenylene pyromellitamic diethyl ester) (PMDA-3,4'-ODA PAE) was chosen as a PAE precursor, and its thermal imidization behavior in microscale thin films was investigated quantitatively for the first time using time-resolved infrared (IR) spectroscopy. In addition, the variations of the film refractive index and thickness with temperature and time were determined in detail from the time-resolved IR spectra and are fully interpreted in this paper by considering the imidization kinetics of the precursor.
引用
收藏
页码:6081 / 6085
页数:5
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