Distinct solvent-dependent luminescence sensing property of a newly constructed Cu(ii)-organic framework

A novel luminescent Cu(ii)-organic framework, {[Cu(asba)(3bpmo)(0.5)(H2O)]center dot H2O}(n) (1), was obtained through the assembly between copper(ii) and 2-amino-5-sulfobenzoic acid (H(2)asba) in the presence of an auxiliary flexible ligand, N,N '-bis(3-pyridylmethyl)oxalamide (3bpmo). 1 is a 2D (6, 3) topological network, which further extends into a 3D supramolecular network via hydrogen and chalcogen bonds. An indirect bandgap exists in 1. 1 shows high framework stability in common solvents and reversible dehydration-rehydration behaviour. Remarkably, 1 is an especially rare example that exhibits novel solvent-dependent luminescence sensing properties. In DMF, 1 shows selective and sensitive fluorescence turn-off sensing of Fe3+ over a number of coexistent metal cations. 1 could also be used as a potential selective and sensitive probe for HCO3- among a variety of interfering anions. Furthermore, 1 shows discriminative sensing of HCO3- over CO32-. In water, 1 shows a quite different fluorescence sensing behaviour from that in DMF. 1 cannot sense Fe3+ and HCO3- in aqueous medium. It is fascinating that 1 shows selective and efficient fluorescence turn-on sensing of Al3+ accompanied by a bathochromic shift of the emission peak in water. The limit of detection (LOD) for Al3+ reaches the 0.80 mu M (0.02 ppm) level.

Automated summary

A novel luminescent Cu(II)-organic framework with unique solvent-dependent luminescence sensing properties has been synthesized, showing selective and sensitive fluorescence turn-off sensing of Fe3+ and HCO3- in DMF. Additionally, the framework exhibits discriminate sensing of HCO3- over CO32- and efficient fluorescence turn-on sensing of Al3+ in water with a low LOD of 0.80 μM.