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New polyimides incorporated with diphenylpyrenylamine unit as fluorophore and redox‐chromophore
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Citations
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References
2011
Year
High Thermal StabilityAromatic DianhydridesEngineeringResponsive PolymersOrganic ChemistryChemistryPolymersChemical EngineeringPolymer TechnologyNew PolyimidesHybrid MaterialsPolymer ChemistryFluorous SynthesisNovel PolyimidesBiomolecular EngineeringPolymer ScienceConjugated PolymerFunctional PolymerOrganic-inorganic Hybrid Material
Abstract A series of novel polyimides based on N,N ‐di(4‐aminophenyl)‐1‐aminopyrene and aromatic or alicyclic tetracarboxylic dianhydrides were synthesized. The polymers exhibited good solubility in many polar organic solvents and could afford robust films via solution casting. The polyimides derived from aromatic dianhydrides exhibited high thermal stability and high glass‐transition temperatures (333–364 °C). Cyclic voltammetry studies of the polymer films showed that these polyimides are both p and n dopable and have multicolored electrochromic states. For the polyimides derived from alicyclic dianhydrides, they revealed a strong blue‐light emission with high fluorescence quantum yields (ϕ PL > 45%) and a marked solvatochromic behavior. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011
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