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Synthesis and characterization of optically active polyimides and their octa(aminophenyl)silsesquioxane nanocomposites
New optically active diamine (3,5-diaminophenyl)((R)-3,4-dihydro-1-phenylisoquinoline-2(1H)-yl)methanone was successfully prepared. Optically active polyimides (PIs) were synthesized by reacting the prepared diamine with the aromatic tetracarboxylic dianhydrides, namely, 3,3′,4,4′-benzophenone tetra...
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Published in: | High performance polymers 2016-06, Vol.28 (5), p.547-561 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | New optically active diamine (3,5-diaminophenyl)((R)-3,4-dihydro-1-phenylisoquinoline-2(1H)-yl)methanone was successfully prepared. Optically active polyimides (PIs) were synthesized by reacting the prepared diamine with the aromatic tetracarboxylic dianhydrides, namely, 3,3′,4,4′-benzophenone tetracarboxylic dianhydride/pyromelltic dianhydride by thermal imidization method and characterized using Fourier transform infrared and nuclear magnetic resonance spectral techniques. Additionally, PI nanocomposites were also prepared by incorporating amino-functionalized polyhedral oligomeric silsesquioxane named as octa(aminophenyl)silsesquioxane (OAPS). The cut-off wavelengths of PIs and their nanocomposites were found to be less than 350 nm, indicating that the PIs are transparent. The PIs and their nanocomposites were found to have glass transition temperature between 204°C and 269°C (differential scanning calorimetric analysis). The 10% weight loss temperature and char yield were found to be 319.5–420.3°C and 26.3–62.7%, respectively. The PIs were found to be amorphous as indicated by X-ray analysis. The scanning electron microscopic images of the nanocomposites also reveal uniform distribution of the nanoparticles in the nanocomposite. PIs and PI/OAPS nanocomposites were found to have low dielectric constant in the range of 2.59–3.36. |
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ISSN: | 0954-0083 1361-6412 |
DOI: | 10.1177/0954008315591021 |