2020
DOI: 10.1021/acsomega.0c04526
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A Multifunctional Tb-MOF Detector for H2O2, Fe3+, Cr2O72–, and TPA Explosive Featuring Coexistence of Binuclear and Tetranuclear Clusters

Abstract: A novel three-dimensional microporous terbium-(III) metal−organic framework (Tb-MOF) named as [Tb 10 (DBA) 6 (OH) 4 (H 2 O) 5 ]•(H 3 O) 4 (1), was successfully obtained by a solvothermal method based on terbium nitrate and 5-di(2′,4′dicarboxylphenyl) benzoic acid (H 5 DBA). The Tb-MOF has been characterized by single crystal X-ray diffraction, elemental analysis, thermogravimetry, and fluorescence properties, and the purity was further confirmed by powder X-ray diffraction (PXRD) analysis. Structural analysis … Show more

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Cited by 38 publications
(16 citation statements)
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“…Tb(2) was coordinated with eight oxygen atoms (Tb-O ¼ 2.26-2.53 Å) from four di-monodentate carboxyl groups in different ligands, one bi-dentate carboxyl group, and two water molecules, which was similar to some other works of Tb-MOFs reported before. 27 Tb(1) and Tb(2) were linked through two dimonodentate carboxyl groups and on m 2 -oxygen atom of the didentate carboxy group. The two adjacent Tb(1) centers were bridged by four di-monodentate carboxyl groups, forming a paddle wheel dinuclear Tb(2) core by which the two Tb(1)-Tb(2) units were linked to form a zigzag tetra-nuclear unit.…”
Section: Resultsmentioning
confidence: 99%
“…Tb(2) was coordinated with eight oxygen atoms (Tb-O ¼ 2.26-2.53 Å) from four di-monodentate carboxyl groups in different ligands, one bi-dentate carboxyl group, and two water molecules, which was similar to some other works of Tb-MOFs reported before. 27 Tb(1) and Tb(2) were linked through two dimonodentate carboxyl groups and on m 2 -oxygen atom of the didentate carboxy group. The two adjacent Tb(1) centers were bridged by four di-monodentate carboxyl groups, forming a paddle wheel dinuclear Tb(2) core by which the two Tb(1)-Tb(2) units were linked to form a zigzag tetra-nuclear unit.…”
Section: Resultsmentioning
confidence: 99%
“…The peak detected at 510 nm is an overtone peak of the excitation wavelength (254 nm). The green luminescence band at 545 nm has the strongest intensity, originating from the metal–organic framework, which induces a hypersensitive electron transition from 5 D 4 to 7 F 5 . The H 4 btec ligand exhibits an emission peak at 330 nm, which is attributed to the π–π transition .…”
Section: Resultsmentioning
confidence: 99%
“…The green luminescence band at 545 nm has the strongest intensity, originating from the metal−organic framework, which induces a hypersensitive electron transition from 5 D 4 to 7 F 5 . 56 The H 4 btec ligand exhibits an emission peak at 330 nm, which is attributed to the π−π transition. 57 However, the emission of the ligand was not observed in the solid-state luminescence spectrum of Tb-MOF.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Therefore, the fluorescence quenching mechanism of this system might be due to the fact that H 2 O 2 of the nucleophile contained unstable O–O bonds, which made the nonbonding orbital and suboxygen atoms form an α effect and further led to the formation of hydrogen bonds between the organic ligands and H 2 O 2 . This weakened the energy transfer from the ligand to Gd 3+ . Subsequently, through analysis of the influence of the concentration of H 2 O 2 on the complex (Figure S7), it could be seen that the luminous intensity of Gd-MOF decayed exponentially with the concentration of H 2 O 2 , and the nonlinear equation was ( R 2 = 0.9986; Figure b).…”
Section: Results and Discussionmentioning
confidence: 99%