Zr(IV)-Based Metal-Organic Framework with T-Shaped Ligand: Unique Structure, High Stability, Selective Detection, and Rapid Adsorption of Cr2O72- in Water.
ACS Appl Mater Interfaces
; 10(19): 16650-16659, 2018 May 16.
Article
em En
| MEDLINE
| ID: mdl-29733570
ABSTRACT
Dichromate is known for severe health impairments to organisms. New and valid strategies have been developed to rapidly detect and efficiently remove this pollutant. Constructing stable luminescent metal-organic frameworks (MOFs) for dichromate recognition and removal from aqueous solution could provide a feasible resolution to this problem. Herein, a new luminescent Zr(IV)-MOF, Zr6O4(OH)7(H2O)3(BTBA)3 (BUT-39, BUT = Beijing University of Technology) was constructed through the reaction of a newly designed functionalized T-shaped ligand 4,4',4â³-(1 H-benzo[ d]imidazole-2,4,7-triyl)tribenzoic acid (H3BTBA) with zirconium salt. BUT-39 has a unique porous framework structure, in which Zr6 cluster acts as a rare low-symmetric 9-connected node and BTBA3- as a T-shaped 3-connected linker. As far as we know, this represents the first case of a (3,9)-connected Zr(IV)-MOF. BUT-39 could retain its framework integrity in boiling water, 2 M HCl aqueous solution, and pH 12 NaOH aqueous solution. Due to its good water stability and strong fluorescent emission, BUT-39 is then employed in fluorescence sensing for various ions in aqueous solution and shows good performance toward Cr2O72- selectively, at a low concentration and a short response time (<1 min). Simultaneously, it also exhibits excellent capacity to rapidly capture Cr2O72- (within 1 min) with a high uptake up to 1 mmol g-1. Taking advantage of its excellent stability, sensitive and selective sensing, as well as rapid and high adsorption, BUT-39 is expected to be useful in Cr2O72- detection in and removal from water.
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1
Coleções:
01-internacional
Base de dados:
MEDLINE
Tipo de estudo:
Diagnostic_studies
Idioma:
En
Revista:
ACS Appl Mater Interfaces
Assunto da revista:
BIOTECNOLOGIA
/
ENGENHARIA BIOMEDICA
Ano de publicação:
2018
Tipo de documento:
Article