Hostname: page-component-8448b6f56d-m8qmq Total loading time: 0 Render date: 2024-04-20T02:22:29.353Z Has data issue: false hasContentIssue false
  • English
  • Français

The Synthesis of Diphenylpolenes and PPV-Oligomers Incorporating Diphenylphosphino Donor Groups

Published online by Cambridge University Press:  10 February 2011

L. G. Madrigal  and
C.W. Spangler
L. G. Madrigal
Affiliation:
Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717
C.W. Spangler
Affiliation:
Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717
Get access

Abstract

Previous studies of the second and third order nonlinear optical properties of organic molecules have shown enhancement of the nonlinear response when second row elements replace first row elements (e. g. S for O) in electron donating groups. Various substituted amino functionalities have been utilized extensively as strong donors in the design of molecules for both second and third order NLO applications. However, to date, no research groups have reported a systematic study of the effect of replacing N (nitrogen) by P (phosphorus) in various chromophore functionalities. We have now synthesized a series of bis(diphenylphosphio)diphenylpolyenes with up to five double bonds, a bis-(diphenylphosphino)-PPV dimer, and a diphenylphosphino DANS equivalent. The absorption characteristics compared to the N equivalents, and the implications for photonics applications will be discussed.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 561: Symposium F – Organic Nonlinear Optical Materials and Devices , 1999 , 75
Copyright
Copyright © Materials Research Society 1999

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1 Cheng, L.-T., Tam, W., Marder, S. R., Stiegmann, A. E., Rikken, G. and Spangler, C. W., J. Phys. Chem. 95, p. 10643 (1991).Google Scholar
2 Marder, S. R., Beratan, D. N. and Cheng, L.-T., Science 252, p. 400 (1991)Google Scholar
3 Spangler, C. W., Faircloth, T., Elandaloussi, E. H., and Reeves, B., Mat. Res. Soc. Symp. Proc. 488, p. 283 (1998).Google Scholar
4 Ehrlich, J. E., Wu, X. L., Lee, I-Y. S., Heikal, A. A., Hu, Z.-Y., Rockel, H., Marder, S. R. and Perry, J. W., Mat. Res. Soc. Symp. Proc. 479, p. 9 (1997).Google Scholar
5 Natarajan, L. V., Private communication.Google Scholar
6 Spangler, C. W., McCoy, R. K., Dembek, A. A., Sapochak, L., and Gates, B. D., J. Chem. Soc. Perkin Trans. 1, p. 186 (1991)Google Scholar
7 Imamoto, T., Oshiki, T., Onozawa, T., Kusumoto, T. and Sato, K., J. Am. Chem. Soc. 112, p. 5244 (1990).Google Scholar