Synthesis of asymmetric biphenyl derivatives for optoelectronic applications
Source abstract
Abstract
Abstract We report the synthesis and optical properties of a series of ten organic compounds with biphenyl as the backbone and asymmetrically modified by triphenylamines, carbazoles and tetraphenylsilanes (BP 1-10). BP 1-10 were synthesized mainly by Ullmann coupling reaction and Suzuki cross-coupling reaction and characterized by EA, NMR, MS, UV–Vis, DSC, TGA, fluorescence spectra and cyclic voltammetry. They exhibit reversible electrochemical behavior with low oxidation potentials and emit intense pure-blue light with high fluorescence quantum yields (up to 80%). BP 1 was fabricated into multi-layered light-emitting diodes as blue-emitting, host and hole transport materials. Based on the performance of BP 1 and the similarity in chemical structure to those compounds reported in literature, these compounds are expected to be good and versatile hole transport, host and blue emitting materials.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (57)
Show source-provided references
1. Baldo · Nature · 1998 · 395 · 15110.1038/25954 ↗
2. Wang · Chin. Phys. Lett. · 2003 · 20 · 114110.1088/0256-307X/20/7/349 ↗
3. D’Andrade · Chem. Phys. · 2003 · 286 · 32110.1016/S0301-0104(02)00921-7 ↗
4. Adachi · Appl. Phys. Lett. · 2001 · 79 · 208210.1063/1.1400076 ↗
5. Kawamura · J. Appl. Phys. · 2002 · 92 · 8710.1063/1.1479751 ↗
6. Okumoto · Mater. Sci. Eng. B. · 2001 · 85 · 13510.1016/S0921-5107(01)00546-3 ↗
7. Kageyama · IEEE J. Quantum Electronics. · 2010 · 16 · 152810.1109/JSTQE.2009.2039699 ↗
8. Promarak · Thin Solid Films · 2008 · 516 · 288110.1016/j.tsf.2007.05.062 ↗
9. Shirota · J. Mater. Chem. · 2000 · 10 · 110.1039/a908130e ↗
10. Kwon · Appl. Mater. Interfaces · 2012 · 4 · 314110.1021/am300480j ↗
11. Shen · Synth. Met. · 2008 · 158 · 105410.1016/j.synthmet.2008.07.012 ↗
12. Luo · Res. Chem. Intermed. · 2012 · 1568
13. Milette · Soft Matter · 2012 · 8 · 2593
14. Kishikawa · J. Mater. Chem. · 2012 · 22 · 848410.1039/c2jm16359d ↗
15. Zhang · J. Phys. Chem. B. · 2012 · 116 · 207510.1021/jp210764h ↗
16. Lopez-Velazquez · Mol. Cryst. Liq. Cryst. · 2012 · 553 · 17510.1080/15421406.2011.609468 ↗
17. Das · J. Mol. Struct. · 2012 · 1013 · 11910.1016/j.molstruc.2012.01.017 ↗
18. Hsu · Carbon · 2012 · 50 · 89610.1016/j.carbon.2011.09.051 ↗
19. Kress · Beilstein. J. Org Chem. · 2012 · 8 · 37110.3762/bjoc.8.40 ↗
20. Wang · Chem. Res. Chin. Univ. · 2012 · 28 · 334
21. Jin · Synth. Met. · 2002 · 127 · 15510.1016/S0379-6779(01)00612-9 ↗
22. Lee · Thin Solid Films · 2011 · 520 · 9510.1016/j.tsf.2011.06.054 ↗
23. Savvate’ev · Mater. Sci. Eng. B. · 2001 · 85 · 22410.1016/S0921-5107(01)00589-X ↗
24. Promarak · Tetrahedron · 2007 · 63 · 888110.1016/j.tet.2007.06.017 ↗
25. Loiseau · J. Am. Chem. Soc. · 2005 · 127 · 1135210.1021/ja0514444 ↗
26. Feng · Synlett · 2006 · 17 · 2841
27. Promarak · Tetrahedron. Lett. · 2006 · 47 · 894910.1016/j.tetlet.2006.10.031 ↗
28. Liu · Adv. Funct. Mater. · 2007 · 17 · 102810.1002/adfm.200600104 ↗
29. Shih · Org. Lett. · 2006 · 8 · 279910.1021/ol060884c ↗
30. Guan · Org. Electron. · 2006 · 7 · 33010.1016/j.orgel.2006.04.006 ↗
31. Kwon · New. J. Chem. · 2008 · 32 · 136810.1039/b714231e ↗
32. Gudeika · J. Phys. Chem. C. · 2012 · 116 · 1481110.1021/jp303172b ↗
33. Yang · J. Phys. Chem. C. · 2012 · 116 · 1504110.1021/jp3034566 ↗
34. Ning · J. Org. Chem. · 2008 · 73 · 379110.1021/jo800159t ↗
35. Shi · Inorg. Chem. · 2012 · 51 · 649810.1021/ic202624e ↗
36. Makarov · J. Phys. Chem. A. · 2012 · 116 · 378110.1021/jp211878u ↗
37. Kim · Syn. Met. · 2005 · 150 · 2710.1016/j.synthmet.2004.12.017 ↗
38. Duan · Thin Solid Films · 2005 · 478 · 12110.1016/j.tsf.2004.10.023 ↗
39. Jiang · Dyes. Pigments. · 2012 · 92 · 89110.1016/j.dyepig.2011.08.009 ↗
40. Yue · Dyes. Pigments. · 2009 · 83 · 7210.1016/j.dyepig.2009.03.014 ↗
41. Gupta · Dyes. Pigments. · 2011 · 88 · 37810.1016/j.dyepig.2010.08.013 ↗
42. Koene · Chem. Mater. · 1998 · 10 · 223510.1021/cm980186p ↗
43. Dawson · J. Phys. Chem. · 1968 · 72 · 325110.1021/j100855a027 ↗
44. Gilman · J. Am. Chem. Soc. · 1950 · 72 · 99510.1021/ja01158a090 ↗
45. Hung · J. Mater. Chem. · 2012 · 22 · 541010.1039/c2jm15963e ↗
46. Jeon · Adv. Mater. · 2011 · 23 · 143610.1002/adma.201004372 ↗
47. Wei · Adv. Funct. Mater. · 2010 · 20 · 244810.1002/adfm.201000299 ↗
48. Yu · Inorg. Chim. Acta. · 2012 · 390 · 11910.1016/j.ica.2012.04.013 ↗
49. Ho · Chem. Asian. J. · 2009 · 4 · 8910.1002/asia.200800226 ↗
50. Wang · Synth. Commun. · 2011 · 41 · 83210.1080/00397911003706982 ↗
51. Wang · Inorg. Chim. Acta. · 2011 · 370 · 34010.1016/j.ica.2011.01.095 ↗
52. Li · Tetrahedron. Lett. · 2012 · 53 · 342510.1016/j.tetlet.2012.04.049 ↗
53. S.Y. Moon, B.S. Lee, H. Dong, J.C. Park, G.W. Kim, Y.U. Park, J.G. Park, J.U. Ju, H.S. Ji, D.H. Choi, J.H. Park, H.S. Yoo, Repub. Korea. KR 1165698 (2012).
54. S.H. Hwang, Y.K. Kim, Y.H. Kwak, C.H. Lee, U.S. Pat. Appl. Publ., US 20080106188 (2008).
55. Adachi · Appl. Phys. Lett. · 1995 · 66 · 267910.1063/1.113123 ↗
56. Wu · Dyes Pigments · 2013 · 97 · 27310.1016/j.dyepig.2012.12.028 ↗
57. Fang · Synth. Met. · 2005 · 155 · 20610.1016/j.synthmet.2005.08.007 ↗