Dramatic luminescence signal from a Co(ii)-based metal–organic compound due to the construction of charge-transfer bands with Al3+ and Fe3+ ions in water: steady-state and time-resolved spectroscopic studies. (27th February 2020)

• Record Type: Journal Article
• Authors: Daga, Pooja; Majee, Prakash; Singha, Debal Kanti; Manna, Priyanka; Hui, Sayani; Ghosh, Ananta Kumar; Mahata, Partha; Mondal, Sudip Kumar
• Is Part Of: New journal of chemistry. Volume 44:Number 11(2020)
• Page Start: 4376
• Page End: 4385
• Publication Date: 2020-02-27
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d0nj00295j
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : A Co(ii )-based metal–organic compound exhibits luminescence turn-on by Al 3+ and quenching by Fe 3+ due to the formation of charge-transfer complexes/adducts. Abstract : To study the photophysics and understand the mechanism of metal ion sensing, a luminescent cobalt-based metal–organic compound, [Co(bpds)(bdc)(H2 O)2 ]·bpds (1 ), was synthesized at room temperature from 4, 4′-bipyridyl disulphide (bpds) and 1, 4-benzene dicarboxylic acid (bdc) by layer diffusion. Structure determination based on single-crystal X-ray analysis revealed a parallel interpenetrated structure of two-dimensional layers along with a layer of uncoordinated bpds ligand. An aqueous suspension of 1 showed intense blue emission at 421 nm. In the presence of few micromolar of Al 3+ ions, a dramatic change in the luminescence spectrum around an isoemissive point was observed with the appearance of a new peak at 380 nm. A similar phenomenon was observed in the presence of Fe 3+ ions. For other metal ions, no significant changes in the luminescence spectrum of 1 were observed. Detailed lifetime decay analysis and Fourier-transform infrared spectroscopy revealed that Al 3+ ions form charge-transfer complexes (or adducts) with uncoordinated bpds ligands through pyridine nitrogen atoms, resulting in a new emission peak at 380 nm. Time-resolved study revealed that the quenching of luminescence was dynamic in nature and associated with an increase in the non-radiative rate constant. Moreover, the luminescence property of 1 was ultrasensitive to the presence of Al 3+ and Fe 3+ ions in water, even in a mixture of many other ions, with detection limits of 0.35 and 0.25 μM, respectively.