Six isostructural stable lanthanide
metal–organic Frameworks
(Ln-OFs), namely, [Ln(ADBA)(HCOO)(DMF)] (Ln = Sm(1),
Tb(2), Dy(3), Ho(4), Er(5), Eu(6), H2ADBA = 4,4′-(anthracene-9,10-diyl)dibenzoate,
DMF = N,N-dimethylformamide), have
been successfully obtained by the solvothermal method based on an
aromatic carboxylic acid ligand H2ADBA. 1–6 have a similar three dimensional (3D) network structure
with pts topology based on dinuclear metallic clusters
{Ln2}. 1–6 all have excellent
chemical and thermal stabilities, which is beneficial to carrying
out fluorescence sensing and achieving catalytic reactions. 1–6 show admirable fluorescent properties
in aqueous solution and can quickly and efficiently detect Fe3+, Cr2O7
2–, and nitrofurazone
(NZF) with high selectivity and excellent sensitivity. Remarkably,
upon completion of detection, the Cr2O7
2– ion in wastewater can be reduced into Cr3+ by photocatalyst 1, which is ascribed to its broad-range
visible-light absorption and recyclable stability. During the reduction
process, ethanol is an optimal hole scavenger; 1 shows
an excellent convert efficiency (99%), a high rate constant (k) of 0.066 min–1, and a high Cr(VI) reduction
rate of 0.158 mgCr(VI)·g–1
cata·min–1 at pH = 2. Furthermore, photocatalyst 1 can be reused for three cycles without significant loss
of catalytic activity. Until now, it is the first example to report
that the photocatalytic reduction of Cr(VI) is achieved only by using
3D rare earth MOFs without additional photosensitizers and cocatalysts.
The reasonable mechanisms of luminescence sensing and photocatalytic
reaction were also investigated systematically via indispensable testing
technologies and theoretical simulated calculation.