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Analysis of Molecular Aggregation Structures of Fully Aromatic and Semialiphatic Polyimide Films with Synchrotron Grazing Incidence Wide-Angle X-ray Scattering
174
Citations
59
References
2010
Year
Macromolecular ChemistryEngineeringChemistryPolymersMolecular Aggregation StructuresPolymer MaterialHybrid MaterialsPolymer ChemistryMaterials ScienceFully AromaticPolymer AnalysisAl-pi Thin FilmsOrganic Material ChemistryMacromolecular ScienceAggregation StructuresSemialiphatic Polyimide FilmsPolymer SolutionPolymer ScienceApplied PhysicsPolymer PropertyAromatic PolyimidesPolymer Hybrid
The intermolecular aggregation structures of fully aromatic polyimides (Ar-PIs) prepared from pyromillitic dianhydride (PMDA) and those of semialiphatic polyimides (Al-PIs) from 4,4′-diaminocyclohexylmethane (DCHM) were characterized by a grazing incidence wide-angle X-ray scattering (GIWAXS) technique. The aggregation structures of both Ar- and Al-PI thin films formed on Si substrates were identified as a mixture of a liquid-crystalline-like ordered domain and an amorphous matrix. For Ar-PIs whose glass transition temperatures (Tg) are higher than the imidization temperature (Ti), the aggregation structures are significantly influenced by the three-dimensional structures of the PI chain. Rodlike molecular structures with high planarity are prerequisites for the growth of ordered domains of Ar-PIs, whereas an Ar-PI having a bent and nonplanar structure displays the highest intensities of an amorphous halo. In addition, the bulky −CF3 groups in the diamine moiety increase the interchain distance in the ordered domains. On the other hand, for Al-PIs whose Tgs are lower than Ti, the degrees of interchain ordering in the ordered domains were higher than those of Ar-PIs, but the orientation of the ordered domains was decreased significantly by decreasing their Tgs. This is due to the vigorous motion of PI chains during thermal imidization.
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