Hostname: page-component-7bb8b95d7b-495rp Total loading time: 0 Render date: 2024-09-12T11:45:30.715Z Has data issue: false hasContentIssue false

Contributions of Conformational and Structural Defects to the Hyperpolarizabilities of Polymers.

Published online by Cambridge University Press:  26 February 2011

Steven M. Risser
Affiliation:
Pacific Northwest Laboratory Richland, WA 99352.
Kim F. Ferris
Affiliation:
Pacific Northwest Laboratory Richland, WA 99352.
Get access

Extract

The extent of the delocalized π electron network is of prime importance in determining hyperpolarizabilities of conjugated molecules. Thus, for conjugated polymers, disruptions to this continuous order such as structural and/or conformational defects may have a large influence on the hyperpolarizabilities. We have performed semiempirical electronic structure calculations for a series of model compounds such as polyenes and polyphosphazenes to determine the effects of structural and conformational defects on the hyperpolarizabilities. Briefly, we find that structural and conjugational defects enhance the hyperpolarizabilities of polyenes, but have little influence on polyphosphazenes due to their limited π delocalization.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

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] Ferris, K.F. and Risser, S.M., Laser Induced Damage in Optical Materials: 1990. NBS Special Publication, National Bureau of Standards, Washington, D.C.Google Scholar
[2] Su, W.P., Schrieffer, J.R. and Heeger, A. J., Phys. Rev. B 22, 2209 (1980)CrossRefGoogle Scholar
[3] de Melo, C.P. and Silbey, R., J. Chem. Phys., 88, 2558 (1988)CrossRefGoogle Scholar
[4] Streitwolf, H.W., Phys. Status Solid B 127, 11 (1985)CrossRefGoogle Scholar
[5] Pople, J.A. and Beveridge, D., “Approximate Molecular Orbital Theory”Google Scholar
[6] Quantum Chemical Program Exchange, Program #571, “MOPAC 5.0”, Stewart, J.P.P. and Dewar, M.J.S..Google Scholar
[7] Hedberg, J.K. (1955) J. Amer. Chem. Soc. 77, 6491;CrossRefGoogle Scholar
7a Barrow, J., Ebsworth, E.A.V. (1984) J.Chem. Soc., Dalton Trans. 563;Google Scholar
7b Almenningen, A., Hedberg, K., Seip, R. (1960) Acta. Chem.Scand. 17, 2264;Google Scholar
7c Gibbs, G.V., D'Arco, P., Boisen, M.B. (1987) J. Phys. Chem. 91, 5347;CrossRefGoogle Scholar
7d Julian, M.M., Gibbs, G.V. (1988) J. Phys. Chem. 92, 1444.Google Scholar
[8] Kurtz, H.A., Stewart, J.J.P. and Dieter, K.M., J. Comp. Chem. 11, 82 (1990).Google Scholar
[9] Risser, S.M. and Ferris, K.F., Chem. Phys. Lett 170, 349 (1990).CrossRefGoogle Scholar
[10] Risser, S., Klemm, S., Allender, D.W. and Lee, Michael A., Mol. Crys. Liq. Crys. 150b, 631 (1987).Google Scholar