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Synthesis and Characterization of Blue Light Emitting N,N-Dimethylpyren-1-Amine and its Vinyl Polymer

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Abstract:

A new small molecule N,N-dimethylpyren-1-amine (DMPA) was synthesized and its vinyl polymer poly(N,N-dimethylpyren-1-amine) was polymerized by free radical polymerization. The chemical structure and properties of DMPA and P(DMPA) were characterized by NMR, GPC, TGA, DSC, UV-Vis, PL, CV and quantum yield measurements.

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Periodical:

Advanced Materials Research (Volumes 557-559)

Pages:

722-726

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.557-559.722

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Online since:

July 2012

Authors:

Jian Li Wang, Louis M Leung

Keywords:

Blue-Light Emitting, Free Radical Polymerization, N,N-Dimethylpyren-1-Amine, Polymer

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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References

[1] Shirota, Y.: J. Mater. Chem. Vol. 10 (2000), p.1

Google Scholar

[2] Chen C. H., J. Shi and C. W. Tang: Macromol. Symp. Vol. 125 (1997), p.1

Google Scholar

[3] Kim Soo-Kang, Bing Yang and Young-Il Park: Org. Electron. Vol. 10 (2009), p.822

Google Scholar

[4] Tao Silu, Ziruo Hong and Zhaokuai Peng: Chem. Phys. Lett. Vol. 397 (2004), p.1

Google Scholar

[5] Kim Y., K. Han and C. S. Ha: Macromolecules Vol. 35 (2002), p.8759

Google Scholar

[6] Kim Y., K. H. Bae and Y. Y. Jeong: Chem. Mater. Vol. 16 (2004), p.5051

Google Scholar

[7] Mitschke U., P. Bäuerle: J. Mater. Chem. Vol. 10 (2000), p.1471

Google Scholar

[8] Segura J. L., N. Martin: J. Mater. Chem. Vol. 10 (2000), p.2403

Google Scholar

[9] Kraft A., A. C. Grimsdale and A. B. Homles: Angew. Chem., Int. Ed. Vol. 37 (1998), p.402

Google Scholar

[10] Gu Cheng, Teng Fei and Ming Zhang: Electrochem. Commun. Vol. 12 (2010), p.553

Google Scholar

[11] Lee D.-H., J.S. Choi and H. Chae: Curr. Appl. Phys. Vol. 9 (2009), p.161

Google Scholar

[12] Mikroyannidis John A., Peter G. Persephonis and Vassilis G. Giannetas: Synth. Met. Vol. 148 (2005), p.293

Google Scholar

[13] Mikroyannidis John A.: Synth. Met. Vol. 155 (2005), p.125

Google Scholar

[14] Tang C., F. Liu and Y.-J. Xia: Org. Electron. Vol. 7 (2006), p.155

Google Scholar

[15] Shimizu H., K. Fujimoto and M. Furusyo: J. Org. Chem. Vol. 72 (2007), p.1530

Google Scholar

[16] Hancock Jessica M., Angela P. Gifford and Christopher J. Tonzola: J. Phys. Chem. C. Vol. 111 (2007), p.6875

Google Scholar

[17] Lo M. Y., C. Zhen and Michael Lauters: J. Am. Chem. Soc. Vol. 129 (2007), p.5808

Google Scholar

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