A hydrostable Cucoordination network prepared hydrothermally as a "turn-on" fluorescent sensor for Sand a selective adsorbent for methylene blue
Dalton Transactions, ISSN: 1477-9234, Vol: 51, Issue: 7, Page: 2962-2974
2022
- 8Citations
- 6Captures
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef8
- Captures6
- Readers6
Article Description
The effective monitoring of water pollution and further purification are pressing yet challenging issues for guaranteeing the health of human beings and the stabilization of ecological systems. For this purpose, the development of efficient sensing and adsorption materials as a result of supramolecular interactions, including coordination and H-bonding etc., have been attracting increasing attention. With the aid of a coordination-driven self-assembly strategy, a new nonporous 2D CuII coordination network, [Cu2L(H2O)2]n (donated as CuCP), based on H4L, where H4L = 4-(4-(3,5-di-carboxy-pyridin-4-yl)phenyl)pyridine-2,6-dicarboxylic acid, was afforded hydrothermally. Structural analysis indicated that CuCP featured a wrinkled network similar to the ancient Chinese folding screens and constructed by the fully deprotonated ligand L4- with the coordination mode of bis(μ2-η1:η1:η2) and penta-coordinated Cu2+, which could be further upgraded to a supramolecular 3D framework as a result of the synergism of multiple C-H⋯O hydrogen bonds. The hydrostability of CuCP could be maintained within a wide pH range from 2 to 12 as verified by PXRD determination, endowing it with potential environmental applications. Thanks to the combination of the soft Lewis acidity of Cu2+ and its large conjugated structure, CuCP could be used as a turn-on fluorescence sensor for S2- and exhibited a different fluorescence response when Na2S, (NH4)2S or H2S were incorporated, even in actual water samples. The sensing mechanisms were disclosed in detail by the combination of experiments and density functional theory (DFT) calculations. Furthermore, CuCP was shown to be a selective and recoverable adsorbent with a maximum adsorption capacity of 379 mg g-1 in 60 minutes for methylene blue (MB). The adsorption mechanism could be a combination of π⋯π stacking, n⋯π interaction, aggregation effects and Soft and Hard Acid-Base theory (HSAB). The results presented herein open up new perspectives for CuII species in environmental applications.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85124636400&origin=inward; http://dx.doi.org/10.1039/d1dt04283a; http://www.ncbi.nlm.nih.gov/pubmed/35108721; https://xlink.rsc.org/?DOI=D1DT04283A; https://dx.doi.org/10.1039/d1dt04283a; https://pubs.rsc.org/en/content/articlelanding/2022/dt/d1dt04283a
Royal Society of Chemistry (RSC)
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