Porous liquids (PLs) are attractive materials because
of their
capability to combine the intrinsic porosity of microporous solids
and the processability of liquids. Most of the studies focus on the
synthesis of PLs with not only high porosity but also low viscosity
by considering their transportation in industrial plants. However,
a gap exists between PLs and solid adsorbents for some practical cases,
where the liquid characteristics and mechanical stability without
leakage are simultaneously required. Here, we fill in this gap by
demonstrating a new concept of pore-networked gels, in which the solvent
phase is trapped by molecular networks with accessible porosity. To
achieve this, we fabricate a linked metal–organic polyhedra
(MOPs) gel, followed by exchanging the solvent phase with a bulky
liquid such as ionic liquids (ILs); the dimethylformamide solvent
trapped inside the as-synthesized gel is replaced by the target IL,
1-butyl-3-methylimidazolium tetrafluoroborate, which in turn cannot
enter MOP pores due to their larger molecular size. The remaining
volatile solvents in the MOP cavities can then be removed by thermal
activation, endowing the obtained IL gel (Gel_IL) with
accessible microporosity. The CO2 capacities of the gels
are greatly enhanced compared to the neat IL. The exchange with the
IL also exerts a positive influence on the final gel performances
such as mechanical properties and low volatility. Besides ILs, various
functional liquids are shown to be amenable to this strategy to fabricate
pore-networked gels with accessible porosity, demonstrating their
potential use in the field of gas adsorption or separation.