We
report the construction of frustrated Lewis pairs (FLPs) in
a metal–organic framework (MOF), where both Lewis acid (LA)
and Lewis base (LB) are fixed to the backbone. The anchoring of a
tritopic organoboron linker as LA and a monotopic linker as LB to
separate metal oxide clusters in a tetrahedron geometry allows for
the precise control of distance between them. As the type of monotopic
LB linker varies, pyridine, phenol, aniline, and benzyl alcohol, a
series of 11 FLPs were constructed to give fixed distances of 7.1,
5.5, 5.4, and 4.8 Å, respectively, revealed by 11B–1H solid-state nuclear magnetic resonance spectroscopy. Keeping
LA and LB apart by a fixed distance makes it possible to investigate
the electrostatic effect by changing the functional groups in the
monotopic LB linker, while the LA counterpart remains unaffected.
This approach offers new chemical environments of the active site
for FLP-induced catalysis