The microporosity of two microporous polymer networks is investigated in detail. Both networks are based on a central spirobifluorene motif but have different linker groups, namely, imide and thiophene units. The microporosity of the networks is based on the polymers of intrinsic microporosity (PIM) design strategy. Nitrogen, argon, and carbon dioxide were used as sorbates in order to analyze the microporosity in greater detail. The gas sorption data was analyzed with respect to important parameters such as specific surface area, pore volume, and pore size (distribution). Ins shown that the results can be strongly model dependent and swelling effects have to be regarded. Xe-129 NMR was used as an independent technique for the estimation of the average pore size of the polymernetworks. The results indicate that both networks are mainly ultramicroporous (pore sizes < 0.8 rim) in the dry state, which was not expected based on the molecular design. Phase separation and network defects might influence the overall network morphology strongly. Finally, the observed swelling indicates that this soft microporous matter might have a different micropore size in the solvent swollen/filled state that in the dry state.
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