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Enhanced electro-optic activity and thermal stability by introducing rigid steric hindrance groups into double-donor chromophore
- Source :
- Dyes and Pigments. 159:222-229
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- A series of novel chromophores based on same bis (N,N-diethyl) aniline donor have been synthesized and systematically characterized. Chromophores with rigid steric hindrance groups showed superb thermal stabilities with high thermal decomposition temperatures above 260 °C. Besides, compared with the chromophore (y2) without isolation group, these new chromophores show better intramolecular charge-transfer absorption. Most importantly, the introduction of rigid steric hindrance groups can effectively reduce dipole–dipole interactions to translate their relatively β values into bulk large electro-optic activities. The electro-optic coefficient of poled films containing 25 wt % of these new chromophores doped in amorphous polycarbonate afforded values of 163, 129, 183 and 196 pm V−1 at 1310 nm for chromophores y1-y4 respectively. These results indicated that introducing rigid isolation group to control the shape of chromophores can efficiently reduce intermolecular electrostatic interactions, thus enhancing the macroscopic electro-optic activity. These properties, together with good solubility, suggest the potential use of these chromophores as advanced material devices.
- Subjects :
- Steric effects
Materials science
Process Chemistry and Technology
General Chemical Engineering
Intermolecular force
Thermal decomposition
02 engineering and technology
Chromophore
010402 general chemistry
021001 nanoscience & nanotechnology
Photochemistry
01 natural sciences
0104 chemical sciences
chemistry.chemical_compound
Aniline
chemistry
visual_art
Intramolecular force
visual_art.visual_art_medium
Thermal stability
Polycarbonate
0210 nano-technology
Subjects
Details
- ISSN :
- 01437208
- Volume :
- 159
- Database :
- OpenAIRE
- Journal :
- Dyes and Pigments
- Accession number :
- edsair.doi...........eb1c666dd95e0bbde6c614905001338a
- Full Text :
- https://doi.org/10.1016/j.dyepig.2018.06.015