Abstract
This study explores the structure-property relationships in colorless polyimides (CPIs) synthesized from stereoisomeric (exo- and endo-form) alicyclic dianhydrides, combined with various diamines. The structural configurations of 5,5’-(1,4-phenylene)bis[hexahydro-(3aR,4R,5R,7S,7aS)-rel-4,7-Methanoisobenzofuran-1,3-dione] (BzDA-exo) and 5,5-(1,4-phenylene)bis(hexahydro-4,7-methanoisobenzofuran-1,3-dione) (BzDA-endo) were confirmed as exo- and endo-forms, respectively, through 1H NMR and 2D NOESY NMR analyses. Wide-angle X-ray scattering (WAXS) data revealed that stereoisomeric structures influence polymer chain packing in synthesized CPIs. The investigation extended to the chemical and physical structure-dependent properties such as physical, thermal and optical properties of the PIs. Notably, structure-dependent physical and thermal properties were evident, with a particularly strong structure-property relationship manifesting in the coloration and yellow index (Y.I.) of PIs. These systematic characterizations offer profound insights into the design and optimization of chemical and physical structures in CPIs, highlighting the versatility of stereoisomeric monomers for various applications.
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