Optical Properties of Chromophores with Different Six-Membered N-Heterocyclic Aromatic Ring

Article Preview

Abstract:

A series of intramolecular charge transfer (ICT) molecules containing six-membered N-heterocyclic electron acceptors, as well as their phenyl analogue, have been synthesized. The pyrazine derivatives exhibit the largest quantum yield, stokes shift and the longest emission maxima wavelength due to the appropriate electronegativity of pyrazine, while the triazine derivative has much lower quantum yield due to its too strong ICT. The methyl groups at N-heterocyclic rings also have influence on the optical properties by disturbing the molecular dipole moment.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 236-238)

Pages:

1598-1602

Citation:

Online since:

May 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] B.A. Reinhardt, L.L. Brott, S.J. Clarson, A.G. Dillard, J.C. Bhatt and R. Kannan: Chem. Mater. Vol. 10 (1998), p.1863

Google Scholar

[2] Z.Q. Liu, Q. Fang, D. Wang, D.X. Cao, G. Xue, W.T. Yu, and H. Lei: Chem. Eur. J. Vol. 9 (2003), p.5074

Google Scholar

[3] Y. Ren, X.Q. Yu, D.J. Zhang, D. Wang, M.L. Zhang, G.B. Xu, X. Zhao, Y.P. Tian, Z.S. Shao and M.H. Jiang: J.Mater. Chem. Vol. 12 (2002), p.3431

Google Scholar

[4] D. Patra, A.K. Mishra: Sensors and Actuators B Vol. 80 (2001), p.278

Google Scholar

[5] J.S. Kim, D. Tyler, A. Rose, Z.G. Zhu and T.M. Swager: J. Am. Chem. Soc. Vol. 123 (2001), p.11488

Google Scholar

[6] J. S. Yang, T.M. Swager: J. Am. Chem. Soc. Vol. 120 (1998), p.5321

Google Scholar

[7] C.F.O. Grae, G.B. Silva, F.N. Äuesch, L. Zuppiroli: Eur. Phys. J. E Vol. 18 (2005), p.21

Google Scholar

[8] L. He, L. Duan, J. Qiao, D.Q. Zhang, L.D. Wang, Y. Qiu: Appl Phys A. Vol. 100 (2010), p.1035

Google Scholar

[9] W. Zhang , Y.Z. Cui, S.J. Wang, T.D. Li, R.S. Sun: Huaxue Xuebao Vol. 67 (2009), p.1880, ( In Chinese )

Google Scholar

[10] C.J. Zhang, M.J. Zhang, W. Yu: Inorganic Chemistry Communications Vol. 13 (2010), p.81

Google Scholar

[11] D.F. Liu, X.Y. Jiang, M. Zhao: Tuliao Gongye Vol. 36 (2006), p.4, ( In Chinese )

Google Scholar

[12] L. Yin, Y.Z. Cui, Q. Fang, G. Xue, G.B. Xu, W.T. Yu: Chin. Chem. Lett. Vol. 16 (2005), p.739

Google Scholar

[13] Z. Zhang, S. Achilefu: Org.Lett. Vol. 6 (2004), p. (2067)

Google Scholar

[14] M. Albota, D. Beljonne, J.L. Bre«das, J.E. Ehrlich, J.Y. Fu, A.A. Heikal, S.E. Hess, T. Kogej, M.D. Levin, S.R. Marder, D.C. Maughon, J.W. Perry, H. Ro¬ckel, M. Rumi, G. Subramaniam, W.W. Webb, X.L. Wu, C. Xu: Science Vol. 281 (1998), p.1653

DOI: 10.1126/science.281.5383.1653

Google Scholar

[15] R. Zbigniew, Grabowski: Pure & Appl. Chem. Vol. 64 (1992), p.1249

Google Scholar