Acetylene is an important industrial gas for the production of
vinyl chloride and 1,4-butynediol, but its storage remains a major
challenge because it is highly explosive. Flexible metal–organic
frameworks (FMOFs) are always at the forefront of porous materials
due to the transformation of the structure under the external stimuli.
In this work, divalent metal ions and multifunctional aromatic N,O-donor
ligands were chosen, and three FMOFs [M(DTTA)2]·guest
[M = Mn (1), Cd (2), and Cu (3)] (H2DTTA = 2,5-bis(1H-1,2,4-trazol-1-yl)
terephthalic acid) have been successfully constructed. Single-crystal
X-ray diffractions show that these compounds are isostructural and
feature a three-dimensional framework. Topological analysis shows
a (4, 6)-connected network with a Schläfli symbol of {44.610.8}{44.62}. All three
compounds exhibit breathing behavior on N2 adsorption at
77 K, and due to the difference of ligand torsion angles, compounds 2 and 3 exhibit extraordinary adsorptions for
C2H2 of 101 and 122 cm3 g–1 at 273 K under 1 bar, respectively. Compared with previous work,
successfully obtaining compound 3 with an innovative
structure can be attributed to the solvent-induced effect in the process
of crystal synthesis, leading to the structure transformation promoting
the significantly increased C2H2 adsorption
performance. This study provides a platform for improvement of synthetic
structures, which can effectively boost gas adsorption performance.