We report the synthesis and properties of network polymers of intrinsic microporosity (network−PIMs) derived from triptycene monomers that possess alkyl groups attached to their bridgehead positions. Gas adsorption can be controlled by the length and branching of the alkyl chains so that the apparent BET surface area of the materials can be tuned within the range 618−1760 m2 g−1. Shorter (e.g., methyl) or branched (e.g., isopropyl) alkyl chains provide the materials of greatest microporosity, whereas longer alkyl chains appear to block the microporosity created by the rigid organic framework. The enhanced microporosity, in comparison to other PIMs, originates from the macromolecular shape of the framework, as dictated by the triptycene units, which helps to reduce intermolecular contact between the extended planar struts of the rigid framework and thus reduces the efficiency of packing within the solid. The hydrogen adsorption capacities of the triptycene-based PIMs with either methyl or isopropyl substituents are among the highest for purely organic materials at low or moderate presures (1.83% by mass at 1 bar/77K; 3.4% by mass at 18 bar/77 K). The impressive hydrogen adsorption capacity of these materials is related to a high concentration of subnanometre micropores, as verified by Horvath−Kawazoe analysis of low-pressure nitrogen adsorption data.

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Quick on the uptake: Following its identification during a targeted search, the intriguing crystal structure of 3,3′,4,4′‐tetra(trimethylsilylethynyl)biphenyl was investigated. Simple removal of the included solvent provides an organic crystal with an open microporous structure that has a striking similarity to that of zeolite A (see picture). Reversible adsorption of nitrogen and hydrogen gases at 77 K confirms that the microporosity is permanent.

High free volume, film-forming copolymers were prepared in which a proportion of the spirounits of PIM-1 were replaced with units derived from 9,10-dimethyl-9,10-dihydro-9,10-ethanoanthracene-2,3,6,7-tetrol (CO1). A full investigation of free volume, utilizing N 2 sorption, positron annihilation lifetime spectroscopy (PALS), Xe sorption and 129 Xe NMR spectroscopy, was undertaken for copolymer PIM1-CO1-40 (spiro-units:CO1 = 60:40) and a comparison is made with PIM-1. All techniques indicate that the copolymer, like PIM-1, possesses free volume holes or pores on the nanometre length scale (i.e., microporosity as defined by IUPAC). For the batch of PIM-1 studied here, the sample as received showed anomalous N 2 sorption, Xe sorption and 129 Xe NMR behavior that could be interpreted in terms of reduced porosity in the size range 0.6-0.7 nm, as compared to the copolymer. The anomalous behavior was eliminated on conditioning or relaxation of the polymer, e.g., by Xe sorption at 100 °C and 3 bar. PALS for both PIM1-CO1-40 and PIM-1 indicates a maximum in the average free volume hole size, and in the width of the distribution of hole sizes, on increasing temperature. This maximum appears to be a feature of high free volume polymers and may be related to the onset of localized oscillations of backbone moieties.

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