Hybrid ultramicroporous materials (HUMs) are porous coordination
networks composed of combinations of organic and inorganic linker
ligands with a pore diameter of <7 Å. Despite their benchmark
gas sorption selectivity for several industrially relevant gas separations
and their inherent modularity, the structural and compositional diversity
of HUMs remains underexplored. In this contribution, we report a family
of six HUMs (
SIFSIX-22-Zn
,
TIFSIX-6-Zn
,
SNFSIX-2-Zn
,
GEFSIX-4-Zn
,
ZRFSIX-3-Zn
, and
TAFSEVEN-1-Zn
) based on Zn metal centers and the
tetratopic N-donor organic ligand tetra(4-pyridyl)benzene (
tepb
). The incorporation of fluorinated inorganic pillars (SiF
6
2–
, TiF
6
2–
, SnF
6
2–
, GeF
6
2–
,
ZrF
6
2–
, and TaF
7
2–
, respectively) resulted in (4,6)-connected
fsc
topology
as verified using single-crystal X-ray diffraction. Pure-component
gas sorption studies with N
2
, CO
2
, C
2
H
2
, C
2
H
4
, and C
2
H
6
revealed that the large voids and narrow pore windows common
to all six HUMs can be leveraged to afford high C
2
H
2
uptakes while retaining high ideal adsorbed solution theory
(IAST) selectivities for industrially relevant gas mixtures: >10
for
1:99 C
2
H
2
/C
2
H
4
and >5
for 1:1 C
2
H
2
/CO
2
. The approach taken,
systematic variation of pillars with retention of structure, enables
differences in selectivity to be attributed directly to the choice
of the inorganic pillar. This study introduces
fsc
topology
HUMs as a modular platform that is amenable to fine-tuning of structure
and properties.