Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes
© The Royal Society of Chemistry 2015. A series of oligofluorenes bearing two 3,6-dipyrenylcarbazole units as the terminal substituents, namely BPCFn (n = 1-3), were successfully synthesized and characterized as non-doped hole-transporting blue emitters. These molecules showed strong blue emission w...
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th-cmuir.6653943832-389112015-06-16T07:54:34Z Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes Sangchart,T. Niroram,A. Kaewpuang,T. Prachumrak,N. Namuangruk,S. Sudyoadsuk,T. Keawin,T. Saengsuwan,S. Jungsuttiwong,S. Maensiri,S. Kungwan,N. Promarak,V. Chemistry (all) Chemical Engineering (all) © The Royal Society of Chemistry 2015. A series of oligofluorenes bearing two 3,6-dipyrenylcarbazole units as the terminal substituents, namely BPCFn (n = 1-3), were successfully synthesized and characterized as non-doped hole-transporting blue emitters. These molecules showed strong blue emission with good solubility, and thermally stable amorphous and excellent film-forming properties. OLEDs using these materials as the emissive layers were fabricated by a simple solution spin-coating process. The blue OLED with excellent device performance (brightness of 6085 cd m-2, luminance efficiency of 4.13 cd A-1 and turn-on voltage of 3.4 V) was attained from BPCF3. 2015-06-16T07:54:34Z 2015-06-16T07:54:34Z 2015-01-01 Article 20462069 2-s2.0-84925278186 10.1039/c5ra02382c http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84925278186&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38911 Royal Society of Chemistry |
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Chemistry (all) Chemical Engineering (all) Sangchart,T. Niroram,A. Kaewpuang,T. Prachumrak,N. Namuangruk,S. Sudyoadsuk,T. Keawin,T. Saengsuwan,S. Jungsuttiwong,S. Maensiri,S. Kungwan,N. Promarak,V. Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
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© The Royal Society of Chemistry 2015. A series of oligofluorenes bearing two 3,6-dipyrenylcarbazole units as the terminal substituents, namely BPCFn (n = 1-3), were successfully synthesized and characterized as non-doped hole-transporting blue emitters. These molecules showed strong blue emission with good solubility, and thermally stable amorphous and excellent film-forming properties. OLEDs using these materials as the emissive layers were fabricated by a simple solution spin-coating process. The blue OLED with excellent device performance (brightness of 6085 cd m-2, luminance efficiency of 4.13 cd A-1 and turn-on voltage of 3.4 V) was attained from BPCF3. |
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Article |
author |
Sangchart,T. Niroram,A. Kaewpuang,T. Prachumrak,N. Namuangruk,S. Sudyoadsuk,T. Keawin,T. Saengsuwan,S. Jungsuttiwong,S. Maensiri,S. Kungwan,N. Promarak,V. |
author_facet |
Sangchart,T. Niroram,A. Kaewpuang,T. Prachumrak,N. Namuangruk,S. Sudyoadsuk,T. Keawin,T. Saengsuwan,S. Jungsuttiwong,S. Maensiri,S. Kungwan,N. Promarak,V. |
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Sangchart,T. |
title |
Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
title_short |
Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
title_full |
Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
title_fullStr |
Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
title_full_unstemmed |
Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
title_sort |
synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes |
publisher |
Royal Society of Chemistry |
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2015 |
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http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84925278186&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38911 |
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1681421559265230848 |