A short review on transparent and colorless polyimides
Author affiliations
DOI:
https://doi.org/10.15625/2525-2518/17017Keywords:
Polyimides, transparent, colorlessAbstract
. Polyimides are known as high performance polymers that are widely used in opto-electronic devices as well as other high engineering applications. Among polyimides, in particular transparent and colorless polyimides (CPIs) are recently in high demand in opto-electronic industries because of their transparency as well as balanced thermo-mechanical properties. It is known that the charge transfer complex (CTC) formation in aromatic polyimides provides them to have brownish-yellow colors as well as optical opaqueness, for which their application in optoelectronic devices are limited, while the CTC also donates a high glass transition temperature (Tg) by restricting their segmental mobility. In this short review, recent trends to prepare CPIs with balanced thermo-mechanical properties were overviewed, which have been reported mainly by our group for years, with expecting to be a useful guideline to the synthesis and design of CPIs. Main efforts to synthesize CPIs have been generally oriented toward to the reduction of the intra- or inter charge transfer interactions between diamines and dianydrides in the aromatic polyimides through the design conceptions including the incorporation of bulky substituents, non-coplanar segments, fluorine atoms, and alicyclic diamines and dianhydrides, etc. to prepare PIs. Thus prepared CPIs possess good transparency and colorlessness with high Tg’s.
Downloads
References
Tapaswi P. K., Ha C. S. - Recent trends on transparent colorless polyimides with balanced thermal and optical properties: design and synthesis, Macromol. Chem. Phys. 220 (2019) 1800313 (1-33).
MacDonald W. A. - Engineered films for display technologies, J. Mater. Chem. 14 (2004) 4-10.
Ito H., Oka W., Goto H., Umeda H. - Plastic substrates for flexible displays, Jpn. J. Appl. Phys. 45 (2006) 4325-4329.
Wakita J., Ando S. - Characterization of electronic transitions in polyimide films based on spectral variations induced by hydrostatic pressures up to 400 mpa, J. Phys. Chem. B 113 (2009) 8835-8846.
Takizawa K., Wakita J., Azami S., Ando S. - Relationship between molecular aggregation structures and optical properties of polyimide films analyzed by synchrotron wide-angle x-ray diffraction, infrared absorption, and uv/visible absorption spectroscopy at very high pressure, Macromolecules 44 (2011) 349-359.
Yi L., Li C., Huang W., Yan D. - Soluble and transparent polyimides with high Tg from a new diamine containing tert-butyl and fluorene units, J. Polym. Sci., Part A: Polym. Chem. 54 (2016) 976-984.
Liaw D. J., Chang F. C., Leung M. K., Chou M. Y., Muellen K. - High thermal stability and rigid rod of novel organosoluble polyimides and polyamides based on bulky and noncoplanar naphthalene-biphenyldiamine, Macromolecules 38 (2005) 4024-4029.
Zhao J., Peng L., Zhu Y., Song Y., Wang L, Shen Y. - Synthesis and memory characteristics of novel soluble polyimides based on asymmetrical diamines containing carbazole, Polymer 91 (2016) 118-127.
Cheng L., Jian X.G. - Synthesis of new soluble aromatic poly(amide imide)s from unsymmetrical extended diamine containing phthalazinone moiety, J. Appl. Polym. Sci. 92 (2004) 1516-1520.
Yeo H., Goh M., Ku B. C. , You N. H. - Synthesis and characterization of highly-fluorinated colorless polyimides derived from 4,4’-((perfluoro–[1,1’–biphenyl]-4,4’-diyl)bis(oxy))bis(2,6-dimethylaniline) and aromatic dianhydrides, Polymer 76 (2015) 280-286.
Ando S., Matsuura T., Sasaki S. - Perfluorinated polyimide synthesis, Macromolecules 25 (1992) 5858-5890.
Liu J. G., He M. H., Zhou H. W., Qian Z. G., Wang F. S., Yang S. Y. - Organosoluble and transparent polyimides derived from alicylic dianhydride and aromatic diamines, J. Polym. Sci., Part A: Polym. Chem. 40 (2002) 110-119.
Ji X., Wang Z., Yan J., Wang Z. - Partially bio-based polyimides from isohexide-derived diamines, Polymer 74 (2015) 38-45.
Hasegawa M., Horiuchi M., Kumakura K., Koyama J. - Colorless polyimides with low coefficient of thermal expansion derived from alkyl-substituted cyclobutanetetracarboxylic dianhydrides, Polym. Int. 63 (2014) 486-500.
Guan Y., Wang D., Song G., Dang G., Chen C., Zhou H., Zhao X. - Novel soluble polyimides derived from 2,2’-bis [4-(5-amino-2-pyridinoxy) phenyl] hexafluoropropane:preparation, characterization, and optical, dielectric properties, Polymer 55 (2014) 3634-3641.
Mathews A. S., Kim I., Ha C. S. - Synthesis, Characterization, and Properties of Fully Aliphatic Polyimides and Their Derivatives for Microelectronics and Optoelectronics Applications, Macromol. Res. 15 (2) (2007), 114-128.
Volksen W., Cha H. J., Sanchez M. I., Yoon D. Y., -Polyimides derived from nonaromatic monomers: synthesis, characterization and potential applications, React. Funct. Polym 30 (1996) 61-69.
Seino H., Sasaki T., Mochizuki A., Ueda M. - Synthesis of fully aliphatic polyimides, High Perform. Polym. 11 (1999) 255-262.
Moon Y. D., Lee Y. M. - Preparation and thermal kinetics of poly(imide-siloxanes), J. Appl. Polym. Sci. 50 (1993) 1461-1473.
Furukawa N., Yamada Y., Furukawa M., Yuasa M., Kimura Y. - Surface and morphological characterization of polysiloxane-block-polyimides, J. Polym. Sci., Part A: Polym. Chem. 35 (1997) 2239-2251
Mathews A. S., Kim I., Ha C. S. - Fully aliphatic polyimides from adamantane-based diamines for enhanced thermal stability, solubility, transparency, and low dielectric constant, J. Appl. Polym. Sci. 102 (2006) 3316-3326.
Chern Y. T., Shiue H. C. - High subglass transition temperatures and low dielectric constants of polyimides derived from 4,9-bis(4-aminophenyl)diamantine, Chem. Mater. 10 (1998) 210-216.
Mathews A. S., Kim I., Ha C. S. - Synthesis and characterization of novel fully aliphatic polyimidosiloxanes based on alicyclic or adamantyl diamines, J. Polym. Sci., Part A: Polym. Chem. 44 (18) (2006) 5254-5270
Rogers F. E. - Polyamide-acids and polyimides from hexafluoropropylidine bridged diamine, U. S. Patent 3,356,648, 1964.
Clair A. K. St., Clair T. L. St., Slemp W. S., Ezzel K. S. - Proceedings of the 2nd International Conference on Polyimides, Ellenville, New York, 1985, pp. 333.
Choi M. C., Wakita J., Ha C. S., Ando S. - Highly transparent and refractive polyimides with controlled molecular structure by chlorine side groups, Macromolecules 42 (2009) 5112-5120
Tapaswi P. K. , Choi M., Jeong K., Ando S., Ha C. S. - Transparent aromatic polyimides derived from thiophenyl-substituted benzidines with high refractive index and small birefringence, Macromolecules 48 (2015) 3462-3474.
Tapaswi P. K., Choi M. C., Nagappan S., Ha C. S. - Synthesis and characterization of highly transparent and hydrophobic fluorinated polyimides from perfluorodecylthio substituted diamine monomers, J. Polym. Sci., Part A Polym. Chem. 53 (2015) 479-488.
Tapaswi P. K., Choi M. C., Jung Y. S., Cho H. J., Seo D. J., Ha C. S. - Synthesis and characterization of fully aliphatic polyimides from an aliphatic dianhydride with piperazine spacer for enhanced solubility, transparency, and low dielectric constant, J. Polym. Sci., Part A: Polym. Chem. 52 (2014) 2316-2328.
Zhang S. J., Bu Q. Q., Li Y. F., Gong C. L., Xu X. Y., Li H. - High organosolubility and optical transparency of novel polyimides derived from 2’,7’-bis(4-amino-2-trifluoromethylphenoxy)-spiro(fluorene-9,9’-xanthene), Mater. Chem. Phys. 128 (2011) 392-399.
Downloads
Published
How to Cite
Issue
Section
License
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Vietnam Journal of Sciences and Technology (VJST) is an open access and peer-reviewed journal. All academic publications could be made free to read and downloaded for everyone. In addition, articles are published under term of the Creative Commons Attribution-ShareAlike 4.0 International (CC BY-SA) Licence which permits use, distribution and reproduction in any medium, provided the original work is properly cited & ShareAlike terms followed.
Copyright on any research article published in VJST is retained by the respective author(s), without restrictions. Authors grant VAST Journals System a license to publish the article and identify itself as the original publisher. Upon author(s) by giving permission to VJST either via VJST journal portal or other channel to publish their research work in VJST agrees to all the terms and conditions of https://creativecommons.org/licenses/by-sa/4.0/ License and terms & condition set by VJST.
Authors have the responsibility of to secure all necessary copyright permissions for the use of 3rd-party materials in their manuscript.