1991 Fiscal Year Final Research Report Summary
Control of Average pi-Conjugation Length in Main-Chain Conjugated Polymers Prepared via Soluble Precursor Route
Project/Area Number |
02650653
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Research Category |
Grant-in-Aid for General Scientific Research (C)
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Allocation Type | Single-year Grants |
Research Field |
高分子物性・高分子材料(含機械材料)
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Research Institution | Kyushu University |
Principal Investigator |
TSUTSUI Tetsuo Kyushu University, Graduate School of Engineering Sciences, Associate Professor, 総合理工学研究科, 助教授 (40037982)
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Project Period (FY) |
1990 – 1991
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Keywords | Soluble Precursor / Conjugated Polymer / Average Conjugation Length / Structural Defect / Polyarylenevinylene |
Research Abstract |
Polyarylenevinylene films with extended pi-conjugated structures were prepared via the organic solvent-soluble precursor route. The method to realize high-quality thin films with extended pi-conjugated structures were investigated. 1. The synthetic methodology to prepare four polyarylenevinylene films (poly (1, 4-phenylenevinylene), poly (2, 3--dimethoxy-1, 4-phenylenevinylene), poly (7, , 5-thienylenevinylene) and poly (2, 5-furyienevinylene)) with high optical qualities were established. 2. The success in both the preparation of precursor polymers with very small chemical defects and the control of conversion from precursor 'Polymer to conjugated polymers enabled the systematic preparation of samples with varied average conjugation lengths. Inspection of UV-visible spectra of polymer films gave the information concerning average conjugation lengths, and IR spectra gave the knowledge on the chemical defects which determined the average conjugation lengths. 3. Oligomer compounds which are the model compounds of poly (2, 5thienylenevinylene) were very useful for identifying structures of defects on conjugated chains. The cis-vinylene linkages were found to be one of the structural defects. 4. Importance of stretching of flexible random coil chains of precursor polymers, when they are converted to rigid linear conjugated chains were understood. The stretching-during-conversion technique was employed to obtain polymer samples with highly extended conjugated structures.
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