Journal of Polymer Science Part A Polymer Chemistry · 2014 · 96 citations · 35 references
Natural SciencesMaterials EngineeringMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsEnergy Storage MaterialsHigh-performance PolymersOrganic Electronic MaterialsPolymer CharacterizationPolymer Thin FilmsCrystallinityCrystallinity AnalysisCrystallinity ChangesElectrical Insulation MaterialsPolar Aprotic SolventsPolyimide SynthesisPolyimidesPolymer Dielectrics
ABSTRACT Three new isomeric diamines containing three, oxy‐linked benzonitriles (3BCN), one of which is asymmetric (meta, para, or m, p), are synthesized in a 3‐step sequence. Polycondensation of these diamines and four common dianhydrides (6FDA, OPDA, BTDA, and PMDA) in N,N ‐dimethylacetamide via poly(amic acid) precursors and thermal curing at temperatures up to 300 °C lead to three series of tough, creasable polyimide (PI) films (tensile moduli = 1.63 − 2.86 GPa). Among these PIs, two PMDA‐based PIs possess relatively high crystallinity and two OPDA‐based PIs, low crystallinity, whereas all 6FDA‐ and BTDA‐based PIs, and m,m ‐3BCN‐OPDA‐PI are amorphous, readily soluble in common polar aprotic solvents. Thermally stable and having high T g (216 − 341 °C), these PIs lose 5% weight around 493–503 °C in air and 463–492 °C in nitrogen. Dielectric properties have been evaluated by broadband dielectric spectroscopy (BDS) and electric displacement‐electric‐field (D‐E) loop measurements. D‐E loop results show an increase in high temperature permittivity (at 190 °C/1 kHz) from 2.9 (for parent PI CP2 with no nitrile group) to as high as 4.9 for these PIs, while keeping their dielectric loss relatively low. Thus, an increase in dipole moment density by the presence of three neighboring CN per repeat unit can increase the overall permittivity, which could be further enhanced by sub‐ T g mobility of para‐phenylene linkages (BDS results). Published 2014. J. Polym. Sci., Part A: Polym. Chem. 2014 J. Polym. Sci., Part A: Polym. Chem. 2015 , 53 , 422–436
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