journal article·2009-12

Blue-light-emitting carbazole derivates with high thermal stability

Zhiyong Yang, Zhenguo Chi, Lin Zhou, Xiqi Zhang, Meina Chen, Bingjia Xu, Chengcheng Wang, Yi Zhang, Jiarui Xu

Optical Materials· Volume 32· Issue 2
Publisher page

Abstract

Abstract A new series of fluorescent compounds containing tricarbazolyl groups have been synthesized. The compounds have very high glass transition temperatures in the range 243–266 °C, high decomposition temperatures of 506–527 °C, and exhibit strong blue fluorescence with maximum emission wavelengths at 445–457 nm. The compounds have good solubility in common solvents even though they contain rather rigid wholly aromatic structures. The thermal stability of these compounds exhibits a marked odd–even effect corresponding to the number of phenylene bridges in the compound. In the solid, the maximum photoluminescence emission wavelength with n odd have a slight bathochromic shift in comparison to those with n even.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (23)

Show source-provided references
1. Shi · Appl. Phys. Lett. · 2002 · 80 · 320110.1063/1.1475361 ↗
2. Culligan · Adv. Funct. Mater. · 2006 · 16 · 148110.1002/adfm.200500785 ↗
3. Chao · Adv. Mater. · 2005 · 17 · 99210.1002/adma.200401476 ↗
4. Kim · Adv. Funct. Mater. · 2005 · 15 · 179910.1002/adfm.200500051 ↗
5. Kim · J. Mater. Chem. · 2007 · 17 · 467010.1039/b706606f ↗
6. Kim · J. Mater. Chem. · 2008 · 18 · 337610.1039/b805062g ↗
7. Song · Tetrahedron Lett. · 2008 · 49 · 358210.1016/j.tetlet.2008.04.015 ↗
8. Wu · Inorg. Chim. Acta · 2007 · 360 · 208310.1016/j.ica.2006.10.043 ↗
9. Fu · Synthetic Met. · 2006 · 156 · 80910.1016/j.synthmet.2006.04.013 ↗
10. Feng · Tetrahedron Lett. · 2006 · 47 · 708910.1016/j.tetlet.2006.07.086 ↗
11. Hyun · Thin Solid Films · 2006 · 209 · 12710.1016/j.tsf.2005.09.084 ↗
12. Justin Thomas · J. Am. Chem. Soc. · 2001 · 123 · 940410.1021/ja010819s ↗
13. Aimono · Appl. Phys. Lett. · 2005 · 86 · 07111010.1063/1.1867555 ↗
14. Kundu · Adv. Funct. Mater. · 2003 · 13 · 44510.1002/adfm.200304308 ↗
15. Demas · J. Phys. Chem. · 1971 · 75 · 99110.1021/j100678a001 ↗
16. Tao · Chem. Phys. Lett. · 2006 · 429 · 62210.1016/j.cplett.2006.08.086 ↗
17. Danel · Chem. Mater. · 2002 · 14 · 386010.1021/cm020250+ ↗
18. Sun · Trans. Met. Chem. · 2007 · 32 · 44910.1007/s11243-007-0186-6 ↗
19. Xu · Eur. J. Org. Chem. · 2008 · 6 · 106510.1002/ejoc.200700981 ↗
20. Zhao · Tetrahedron · 2008 · 64 · 265810.1016/j.tet.2007.12.059 ↗
21. Tao · Synlett · 2004 · 2 · 359
22. Houk · J. Am. Chem. Soc. · 1999 · 121 · 147910.1021/ja982748b ↗
23. Taki · J. Phys. Soc. Jpn. · 1999 · 68 · 128610.1143/JPSJ.68.1286 ↗