Blue-Emitting Carbon- and Nitrogen-Bridged Poly(ladder-type tetraphenylene)s
Source abstract
Abstract
An efficient synthesis has been developed toward two new poly(ladder-type tetraphenylene)s, either with one nitrogen at the bridge-head position or all carbon-bridged, both of which were blue emitters. The two polymers exhibited very narrow emission centered around 445 nm, where the human eye is most sensitive. Polymer light-emitting diodes prepared under inert atmosphere in the standard configuration (indium tin oxide/poly(3,4-ethylenedioxythiophene):polystyrenesulfonic acid/polymer/Ca/Al) demonstrated very high luminance values, typically over 600−900 cd/m 2 at a bias of 10−15 V for the two polymers. The nitrogen-bridged poly(ladder-type tetraphenylene) demonstrated a lower electroluminescence onset voltage and was found to be more stable toward oxidative degradation compared to the all-carbon-bridged analogue, which undergoes oxidative degradation as evidenced by the appearance of a new emission maximum around 575 nm.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Max-Planck-Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany, Christian Doppler Laboratory “Advanced Functional Materials”, Institute of Solid State Physics, Graz University of Technology, Petersgasse 16, A-8010 Graz, Austria, and Institute of Nanostructured Materials and Photonics, Joanneum Research, Franz-Pichler-Strasse 30, A-8160 Weiz, Austria
References (25)
Show source-provided references
1. Mitschke U. · J. Mater. Chem. · 2000 · 10 · 147110.1039/a908713c ↗
2. Kraft A. · Angew. Chem., Int. Ed. · 1998 · 37 · 40210.1002/(SICI)1521-3773(19980302)37:4<402::AID-ANIE402>3.0.CO;2-9 ↗
3. Dimitrakopoulos C. D. · Adv. Mater. · 2002 · 14 · 9910.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-9 ↗
4. McGehee M. D. · J. Adv. Mater. · 2000 · 12 · 165510.1002/1521-4095(200011)12:22<1655::AID-ADMA1655>3.0.CO;2-2 ↗
5. Li J. · J. Mater. Chem. · 2006 · 16 · 9610.1039/B512373A ↗
6. Brabec C. J. · Adv. Funct. Mater. · 2001 · 11 · 1510.1002/1616-3028(200102)11:1<15::AID-ADFM15>3.0.CO;2-A ↗
7. Neher D. · Macromol. Rapid Commun. · 2001 · 22 · 136610.1002/1521-3927(20011101)22:17<1365::AID-MARC1365>3.0.CO;2-B ↗
8. Setayesh S. · Macromolecules · 2000 · 33 · 201610.1021/ma9914366 ↗
9. Jacob J. · J. Am. Chem. Soc. · 2004 · 126 · 698710.1021/ja0398823 ↗
10. Scherf U. · J. Mater. Chem. · 1999 · 9 · 185310.1039/a900447e ↗
11. List E. J. W. · Adv. Mater. · 2002 · 14 · 37410.1002/1521-4095(20020304)14:5<374::AID-ADMA374>3.0.CO;2-U ↗
12. Jacob J. · Macromolecules · 2003 · 36 · 824010.1021/ma034849m ↗
13. Jacob J. · Macromolecules · 2005 · 38 · 993310.1021/ma0517143 ↗
14. Morin J. F. · Macromol. Rapid Commun. · 2005 · 26 · 76110.1002/marc.200500096 ↗
15. Morin J. F. · Macromolecules · 2002 · 35 · 841310.1021/ma020880x ↗
16. Morin J. F. · Macromolecules · 2001 · 34 · 468010.1021/ma010152u ↗
17. Morin J. F. · Macromol. Rapid Commun. · 2002 · 23 · 103210.1002/marc.200290000 ↗
18. Patil S. A. · Adv. Funct. Mater. · 2003 · 13 · 60910.1002/adfm.200304344 ↗
19. Dierschke F. · Macromol. Chem. Phys. · 2004 · 205 · 114710.1002/macp.200300219 ↗
20. Qiu S. · Macromolecules · 2005 · 38 · 678210.1021/ma050821u ↗
21. Dierschke F. · Synthesis · 2003 · 2470
22. Janietz S. · Appl. Phys. Lett. · 1998 · 73 · 245310.1063/1.122479 ↗
23. Mauthner G. · J. Appl. Phys. · 2005 · 97 · 63508110.1063/1.1850172 ↗
24. Gamerith S. · Jpn. J. Appl. Phys. · 2004 · 43 · L89110.1143/JJAP.43.L891 ↗
25. Omhori Y. · Jpn. J. Appl. Phys. · 1991 · 11 · L1941