When a multicarboxylate aromatic
ligand, 3,5-di(2′,4′-dicarboxylphenyl)benzoic
acid (H5L), was employed, five structurally similar lanthanide
metal–organic frameworks (Ln-MOFs), {[Pr10L6(OH)3Cl(H2O)6]·4C2H8N}
n
(1), {[Nd10L6(OH)4 (H2O)9]·4C2H8N}
n
(2), {[Gd10L6(OH)4(H2O)3]·4C2H8N}
n
(3), {[Ho10L6(OH)4 (H2O)3]·4C2H8N}
n
(4) and {[Er10L6(OH)4(H2O)6]·4C2H8N}
n
(5), were synthesized and characterized. Single-crystal
X-ray structural analyses disclosed that all five Ln-MOFs crystallize
in the trigonal R
3 space group. They have
three-dimensional mesoporous structure featuring the coexistence of
binuclear and tetranuclear species as inorganic building units. The
mesoporous structure of 3 was verified by the gas adsorption
experiment of N2. Fluorescence analysis showed that 3 can selectively detect Fe3+, Cr2O7
2–, and H2O2; furthermore,
it can be used for the electrochemical detection of trinitrophenol.
With the merit of an excellent highly sensitive detection performance, 3 has unpredictable application prospects in future research
fields.