Synthesis of a New Monomer: 4,7-bis(5-phenylthiophen-2-yl)benzo[c][1,2,5]selenadiazole

Tao Hu; Li Ping Wang; Xiao Long Lei; Xiao Xia Sun

doi:10.4028/www.scientific.net/AMM.707.28

Paper Titles

Determination of N-Heptyl Pyridine Tetrafluoroborate in Acetonitrile Using UV–Spectrum
p.12

Preparation and Characterization of N-Octyl Pyridine Tetrafluoroborate
p.16

Determination Content of N-Octyl Pyridine Tetrafluoroborate in Water Using UV-Spectrum
p.20

UV-Spectrum Analysis of N-Octyl Pyridine Tetrafluoroborate in Ethanol
p.24

Synthesis of a New Monomer: 4,7-bis(5-phenylthiophen-2-yl)benzo[c][1,2,5]selenadiazole
p.28

Synthesis of Novel Monomer with Quinoxaline Derivatives
p.32

Synthesis and Photochromism Studies of 1-(2-n-butyl-3-benzothienyl)-2-[2-methyl-5-phenyl-3-thienyl] Perfluorocyclopentene
p.36

Synthesis and Photochromism Studies of 1,2-bis[2-methyl-5-(4-bromomethylphenyl)-3-thienyl] Perfluorocyclopentene
p.40

Synthesis and Properties of [1-(3,5-dimethyl-4-iodoisoxazole)-2-(2-methyl-(5-ethynyl)trimethylsilane-3-thienyl)perfluorocyclopentene
p.44

HomeApplied Mechanics and MaterialsApplied Mechanics and Materials Vol. 707Synthesis of a New Monomer:...

Synthesis of a New Monomer: 4,7-bis(5-phenylthiophen-2-yl)benzo[c][1,2,5]selenadiazole

Abstract:

A donor/acceptor/donor-type benzoselenadiazole-incorporated monomer was synthesized. The procedure described herein offer several advantages, including high product yields, easy purification and large scale production. Optical properties of the resulting compounds were examined by means of UV-vis and fluorescence spectroscopies. The fluorescence spectra exhibit that the emission maxima of material at 419 nm belongs to blue light region.

You might also be interested in these eBooks

View Preview

Info:

Periodical:

Applied Mechanics and Materials (Volume 707)

Pages:

28-31

DOI:

https://doi.org/10.4028/www.scientific.net/AMM.707.28

Citation:

Cite this paper

Online since:

December 2014

Authors:

Tao Hu, Li Ping Wang, Xiao Long Lei, Xiao Xia Sun*

Keywords:

[ 2,1,3]-Benzoselenadiazole, Organic Light-Emitting, Stille Reaction, Suzuki Couplling

Export:

RIS, BibTeX

Price:

Permissions CCC:

Request Permissions

Permissions PLS:

Request Permissions

Сopyright:

Citation:

* - Corresponding Author

References

[1] C. W. Tang, S. A. VanSlyke, Appl. Phys. Lett., 51, 913 (1987).

Google Scholar

[2] J. H. Burroughes, D. D. C. Bradley,A. R. Brown, R. N. Marks, K. Mackay, R. H. Friend,; P. L. Burns, A. B. Holmes, Nature, 347, 539 (1990).

DOI: 10.1038/347539a0

Google Scholar

[3] N. C. Greenham, S. C. Moratti, D. D. C. Bradley, R. H. Friend, A. B. Holmes, Nature, 365, 628 (1993).

Google Scholar

[4] R. H. Friend, R. W. Gymer, A. B. Holmes, J. H. Burroughes, R. N. Marks, C. Taliani, D. D. C. Bradley, D. A. Dos Santos, J. L. Bredas, M. Lgdlund, W. R. Salaneck, Nature, 397, 121 (1999).

DOI: 10.1038/16393

Google Scholar

[5] J. Huang, Y. Niu, W. Yang, Y. Mo, M. Yuan, Y. Cao, Macromolecules, 35, 6080 (2002).

Google Scholar

[6] J. Huang, Y. Xu, Q. Hou, W. Yang, M. Yuan, Y. Cao, Macromol. Rapid Commun., 23, 709 (2002).

Google Scholar

[7] A. C. Morteani, A. S. Dhoot, J. -S. Kim, C. Silva, N. C. Greenham, C. Murphy, E. Moons, S. Cina, J. H. Burroughes, R. H. Friend, Adv. Mater., 15, 1708 (2003).

DOI: 10.1002/adma.200305618

Google Scholar

[8] A. C. Arias, J. D. MacKenzie, R. Stevenson, J. J. M. Halls, M. Inbasekaran, E. P. Woo, D. Richards, R. H. Friend, Macromolecules, 34, 6005(2001).

DOI: 10.1021/ma010240e

Google Scholar

[9] C. J. Brabec, C. Winder, N. S. Sariciftci, J. C. Hummelen, A. Dhanabalan, P. A. vanHal, R. A. Janssen, J. Adv. Funct. Mater., 12, 709 (2002).

DOI: 10.1002/1616-3028(20021016)12:10<709::aid-adfm709>3.0.co;2-n

Google Scholar