TY - JOUR
T1 - Conjugated poly-p-phenylene (PPP) from poly(m-cyclohexadiene) (PCHD) homo- and block copolymers
T2 - controlled processability and properties
AU - Mays, J.
AU - Hong, K.
AU - Wang, Y.
AU - Advincula, R. C.
PY - 1999
Y1 - 1999
N2 - 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 homoand 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.
AB - 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 homoand 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.
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M3 - Article
AN - SCOPUS:0033341501
SN - 0272-9172
VL - 561
SP - 189
EP - 194
JO - Materials Research Society Symposium - Proceedings
JF - Materials Research Society Symposium - Proceedings
ER -