Hostname: page-component-84b7d79bbc-g7rbq Total loading time: 0 Render date: 2024-08-04T10:29:11.072Z Has data issue: false hasContentIssue false
  • English
  • Français

Conjugated Poly-P-Phenylene (PPP) From Poly(1,3-Cyclohexadiene) (PCHD) Homo- and Block Copolymers: Controlled Processability and Properties

Published online by Cambridge University Press:  10 February 2011

J. Mays ,
K. Hong ,
Y. Wang  and
R.C. Advincula
J. Mays
Affiliation:
Department of Chemistry, University of Alabama at Birmingham, Chemistry Building, Birmingham, AL 35294-1240
K. Hong
Affiliation:
Department of Chemistry, University of Alabama at Birmingham, Chemistry Building, Birmingham, AL 35294-1240
Y. Wang
Affiliation:
Department of Chemistry, University of Alabama at Birmingham, Chemistry Building, Birmingham, AL 35294-1240
R.C. Advincula
Affiliation:
Department of Chemistry, University of Alabama at Birmingham, Chemistry Building, Birmingham, AL 35294-1240
Get access

Abstract

Conjugated polymers have been used as solid-state materials for a variety of opto-electronic applications. Thus, their processability in a number of device fabrication protocols is an important consideration. In this report, we indicate our results on the synthesis of conjugated poly-p-phenylene (PPP) materials derived from poly(1,3-cyclohexadiene) (PCHD). The precursor PCHD polymers were synthesized by living anionic polymerization to produce homo-and block copolymer configurations with polystyrene. We have used a variety of initiators, solvent, and temperature conditions to determine the right parameters for obtaining narrow MWD polymers. The conditions for polymerization determined the ratio of 1,2 and 1,4 isomers in the microstructure. We then proceeded with conversion to PPP derivatives using a dehydrogenation reaction with chloranil. Our results indicate a systematic conversion to a conjugated polymer with increased solubility and photoluminescence properties. The microstructure, MW and block copolymer composition affecting the processability and conversion properties dramatically.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 561: Symposium F – Organic Nonlinear Optical Materials and Devices , 1999 , 189
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] Ivory, M., Miller, G., Sowa, J., Shacklette, L., Chance, R., Baughman, R., J. Chem. Phys. 7, 1506 (1979).Google Scholar
[2] Grem, G., Leditzky, G., Ullrich, B., Leising, G., Adv. Mater. 4, 36, (1992).Google Scholar
[3] Grem, G., Leditzky, G., Ullrich, B., Leising, G., Synth. Met. 51, 389, (1992).Google Scholar
[4] Marvel, C., Hartzell, G., J. Am. Chem. Soc. 81, 448, (1959).Google Scholar
[5] Natori, I., Inoue, S., Macromolecules 31, 4687, (1998).Google Scholar
[6] David, J., Gido, S., Hong, K., Zhou, J., J. Mays submitted to Macromolecules. Google Scholar
[7] Hong, K., and Mays, J., manuscript in preparation Google Scholar
[8] Lefebvre, G., and Dawans, F., J. Polym. Sci. A: 2, 3277, (1964).Google Scholar
[9] David, J., Gido, S., Hong, K., Zhou, J., Mays, J., Tan, N. Beck, submitted to MacromoleculesGoogle Scholar
[10] Remers, M., Neher, D., Gruner, J., Friend, R., Gelinck, G., Warman, J., Quattrocchi, C., Santos, D. dos, Breda, J., Macromolecules 29, 7432, (1996).Google Scholar