Soluble High Molecular Weight Poly(p-phenylene) as a Charge-Transfer Complex
Soluble high molecular weight poly(p-phenylene) (PPP), in the form of a charge-transfer complex, was synthesized by complete dehydrogenation of poly(1,3-cyclohexadiene) (PCHD) with excess tetrachloro-1,2-(o)-benzoquinone (TOQ). The yield of the PPP-TOQ complex increased as the molecular weight of th...
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Published in | Macromolecules Vol. 42; no. 6; pp. 1964 - 1969 |
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Format | Journal Article |
Language | English |
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American Chemical Society
24.03.2009
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Abstract | Soluble high molecular weight poly(p-phenylene) (PPP), in the form of a charge-transfer complex, was synthesized by complete dehydrogenation of poly(1,3-cyclohexadiene) (PCHD) with excess tetrachloro-1,2-(o)-benzoquinone (TOQ). The yield of the PPP-TOQ complex increased as the molecular weight of the original PCHD increased. The addition of TOQ to the PPP polymer chain occurred mainly at the 1,4-phenylene (Ph) units. The PPP-TOQ complex showed good solubility in tetrahydrofuran; the solubility was not limited by the length of the 1,4-Ph sequence. The formation of the PPP-TOQ complex effectively suppressed crystallization of PPP due to the decrease in π−π intermolecular interactions in the PPP molecules, and had a significant effect on π-orbital conjugation in PPP. |
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AbstractList | Soluble high molecular weight poly(p-phenylene) (PPP), in the form of a charge-transfer complex, was synthesized by complete dehydrogenation of poly(1,3-cyclohexadiene) (PCHD) with excess tetrachloro-1,2-(o)-benzoquinone (TOQ). The yield of the PPP-TOQ complex increased as the molecular weight of the original PCHD increased. The addition of TOQ to the PPP polymer chain occurred mainly at the 1,4-phenylene (Ph) units. The PPP-TOQ complex showed good solubility in tetrahydrofuran; the solubility was not limited by the length of the 1,4-Ph sequence. The formation of the PPP-TOQ complex effectively suppressed crystallization of PPP due to the decrease in π−π intermolecular interactions in the PPP molecules, and had a significant effect on π-orbital conjugation in PPP. |
Author | Natori, Shizue Ogino, Kenji Natori, Itaru |
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Cites_doi | 10.1002/(SICI)1099-0518(199805)36:7<1043::AID-POLA2>3.0.CO;2-3 10.1016/0379-6779(93)90565-E 10.1063/1.438420 10.1002/marc.1988.030090607 10.1002/pi.2214 10.1016/0014-3057(81)90098-7 10.1246/bcsj.43.345 10.1295/polymj.12.771 10.1002/polb.20798 10.1016/j.physb.2006.10.029 10.1016/0379-6779(92)90293-R 10.1002/pola.22668 10.1002/adma.19920040107 10.1002/anie.196808351 10.1002/macp.1991.021921008 10.1021/ma0603478 10.1016/j.polymer.2006.07.069 10.1016/0014-3057(91)90079-4 10.1016/0032-3861(79)90150-2 10.1016/0379-6779(91)91534-H 10.1002/macp.200390048 10.1016/S0379-6779(98)01376-9 10.1016/S0379-6779(96)04100-8 10.1016/0379-6779(89)90272-5 10.1002/pola.22970 10.1021/cr00078a005 10.1002/pola.22851 10.1002/mrc.1270090911 |
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Keywords | Benzoquinone derivatives Photoluminescence Phenylene polymer Experimental study Organic solution Cyclodiene polymer Conjugated polymer Chemical modification Chlorine Organic compounds Preparation Soluble compound Charge transfer compound Aromatic dehydrogenation |
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StartPage | 1964 |
SubjectTerms | Applied sciences Chemical modifications Chemical reactions and properties Exact sciences and technology Organic polymers Physicochemistry of polymers |
Title | Soluble High Molecular Weight Poly(p-phenylene) as a Charge-Transfer Complex |
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