Being not prone to aging and possessing high C ₄ /C ₁ selectivity, new tricyclononene polymers bearing (AlkO) ₃ Si side groups are prospective materials for hydrocarbon mixture separation.

Polynorbornenes are ideal materials for systematic structure–property investigations designed to correlate gas-transport properties to polymer structure. The modular nature of norbornene-based systems provides a facile route towards the synthesis of diverse polymeric materials. Though many valuable correlations between gas-permeability and polynorbornene structure have been summarized in a prior review (2017), many of these efforts focused heavily on the design of materials with high permeabilities. More recently, the design of next-generation polynorbornene membranes has shifted toward the development of materials that are highly selective for multiple targeted gas separations. Since 2017, tremendous progress has been realized in the preparation of stable and highly selective polynorbornenes for membrane-based gas separations. Examples include polynorbornene derivatives that exhibit very high selectivity for CO₂/N₂ and light hydrocarbon (e.g., C₃₊/C₁) separations, some of which exhibit gas separation performances that approach or exceed the 2008 upper bound. Herein, we summarize prior findings, present recent developments in the field of advanced polynorbornene membrane materials for targeted gas separations, and provide an outlook for the future of this field of research.

In recent years, increased attention has been paid to environmental issues and, in connection with this, to the development of hydrogen energy. In turn, this requires the large-scale production of ultra pure hydrogen. Currently, most hydrogen is obtained by converting natural gas and coal. In this regard, the issue of the deep purification of hydrogen for use in fuel cells is very relevant. The deep purification of hydrogen is also necessary for some other areas, including microelectronics. Only palladium membranes can provide the required degree of purification. In addition, the use of membrane catalysis is very relevant for the widely demanded processes of hydrogenation and dehydrogenation, for which reactors with palladium membranes are used. This process is also successfully used for the single-stage production of high-purity hydrogen. Polymeric palladium-containing membranes are also used to purify hydrogen and to remove various pollutants from water, including organochlorine products, nitrates, and a number of other substances.

A simple one-step approach for the selective synthesis of exo-norbornenes with organosilicon substituents is suggested through the direct hydrosilylation of norbornadiene-2,5 with chlorine-free silanes. Using the example of norbornadiene-2,5 hydrosilylation with pentamethyldisiloxane and 1,1,1,3,5,5,5-heptamethyltrisiloxane, the possibility of obtaining exo-isomers of norbornenes with 100 exo-/endo-selectivity is shown. The investigation of Pt-, Rh-, and Pd-complexes in combination with various ligands as catalysts was performed. The hydrosilylation of norbornadiene-2,5 in the presence of Pt- or Rh-catalysts was not selective and led to a mixture consisting of three isomers (exo-/endo-norbornenes and substituted nortricyclane). In the case of the Pd-salt/ligand catalytic system, the formation of an endo-isomer was not observed at all and only two isomers were formed (exo-norbornene and nortricyclane). The selectivity of exo-norbornene/nortricyclane formation strongly depended on the nature of the ligand in the Pd-catalyst. The best selectivity was revealed when R-MOP was the ligand, while the highest catalytic activity was reached with a dioxalane-containing ligand.

New microporous homopolymers were readily prepared from norbornadiene-2,5, its dimer and trimer by addition (vinyl) polymerization of the corresponding monomers with 60–98% yields. As a catalyst Pd-N-heterocyclic carbene complex or Ni(II) 2-ethylhexanoate activated with Na⁺[B(3,5-(CF₃)₂C₆H₃)₄]⁻ or methylaluminoxane was used. The synthesized polynorbornenes are cross-linked and insoluble. They are glassy and amorphous polymers. Depending on the nature of the catalyst applied, BET surface areas were in the range of 420–970 m²/g. The polymers with the highest surface area were obtained in the presence of Pd-catalysts from the trimer of norbornadiene-2,5. The total pore volume of the polymers varies from 0.39 to 0.79 cm³/g, while the true volume of micropores was 0.14–0.16 cm³/g according to t-plot. These polymers gave CO₂ uptake from 1.2 to 1.9 mmol/g at 273 K and 1 atm. The porous structure of new polymers was also studied by means of wide-angle X-ray diffraction and positron annihilation lifetime spectroscopy.