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Enantiomers of 2, 6-diaminotriptycene (R, R-1 and S, S-1) are split by chiral-phase HPLC and their absolute configurations are identified by single-crystal X-ray diffraction technology. Using the enantiomers as monomers, a couple of chiral porous polyimides (R-FTPI and S-FTPI) are prepared by polycondensation reactions and display good heat stability, high BET surface area and good solubility in organic solvents. Moreover, both of R-FTPI and S-FTPI can be cast into robust, free-standing films suitable for enantioselective separation with symmetrical chiral selectivity.
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Zhang et al. (2021) studied this question.
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