| dc.contributor.author | Moroni, Marco | |
| dc.contributor.author | Vismara, Rebecca | |
| dc.contributor.author | Navarro, Jorge A. R. | |
| dc.date.accessioned | 2023-05-23T08:49:07Z | |
| dc.date.available | 2023-05-23T08:49:07Z | |
| dc.date.issued | 2023-03-22 | |
| dc.identifier.citation | Chem. Mater. 2023, 35, 7, 2892–2903[https://doi.org/10.1021/acs.chemmater.2c03801] | es_ES |
| dc.identifier.uri | https://hdl.handle.net/10481/81739 | |
| dc.description.abstract | Mercury is one of the most toxic heavy metals. By virtue of its triple bond, the novel ligand 1,2-bis(1H-pyrazol-4- yl)ethyne (H2BPE) was expressly designed and synthesized to devise metal−organic frameworks (MOFs) exhibiting high chemical affinity for mercury. Two MOFs, Zn(BPE) and Zn(BPE)·nDMF [interpenetrated i-Zn and noninterpenetrated ni-Zn·S, respectively; DMF = dimethylformamide], were isolated as microcrystalline powders. While i-Zn is stable in water for at least 15 days, its suspension in HgCl2 aqueous solutions prompts its conversion into HgCl2@ni-Zn. A multitechnique approach allowed us to shed light onto the observed HgCl2-triggered i-Zn-to- HgCl2@ni-Zn transformation at the molecular level. Density functional theory calculations on model systems suggested that HgCl2 interacts via the mercury atom with the carbon−carbon triple bond exclusively in ni-Zn. Powder X-ray diffraction enabled us to quantify the extent of the i-Zn-to-HgCl2@ni-Zn transition in 100−5000 ppm HgCl2 (aq) solutions, while X-ray fluorescence and inductively coupled plasma-mass spectrometry allowed us to demonstrate that HgCl2 is quantitatively sequestered from the aqueous phase. Irradiating at 365 nm, an intense fluorescence is observed at 470 nm for ni-Zn·S, which is partially quenched for i-Zn. This spectral benchmark was exploited to monitor in real time the i-Zn-to-HgCl2@ni-Zn conversion kinetics at different HgCl2 (aq) concentrations. A sizeable fluorescence increase was observed, within a 1 h time lapse, even at a concentration of 5 ppb. Overall, this comprehensive investigation unraveled an intriguing molecular mechanism, featuring the disaggregation of a water-stable MOF in the presence of HgCl2 and the self-assembly of a different crystalline phase around the pollutant, which is sequestered and simultaneously quantified by means of a luminescence change. Such a case study might open the way to new-conception strategies to achieve real-time sensing of mercury-containing pollutants in wastewaters and, eventually, pursue their straightforward and costeffective purification. | es_ES |
| dc.description.sponsorship | University of Insubria for
partial funding | es_ES |
| dc.description.sponsorship | Programa Juan de la Cierva
Formación (FJC2020-045043-I) | es_ES |
| dc.description.sponsorship | MCIN/AEI/10.13039/501100011033 | es_ES |
| dc.description.sponsorship | European
Union NextGenerationEU/PRTR (Grants PID2020-
113608RB-I00 and TED2021-129886B-C41) | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | ACS Publications | es_ES |
| dc.rights | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.title | Mercury Clathration-Driven Phase Transition in a Luminescent Bipyrazolate Metal−Organic Framework: A Multitechnique Investigation | es_ES |
| dc.type | journal article | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/European Union NextGenerationEU/PID2020- 113608RB-I00 and TED2021-129886B-C41 | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.identifier.doi | 10.1021/acs.chemmater.2c03801 | |
| dc.type.hasVersion | VoR | es_ES |