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A 3D metal-organic framework with isophthalic acid linker for photocatalytic properties
The efficient removal of organic pollutants from wastewater is a hot research topic due to its ecological and environmental importance. Herein, by using the ligand-truncation and functionalization strategy, a Cu(II)-based 3D metal-organic framework (MOF), [Cu2(L1)∙5DMF]n (1) (H4L1 = 3,5-di(3,5-dicar...
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Published in: | Inorganic chemistry communications 2019-02, Vol.100, p.92-96 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The efficient removal of organic pollutants from wastewater is a hot research topic due to its ecological and environmental importance. Herein, by using the ligand-truncation and functionalization strategy, a Cu(II)-based 3D metal-organic framework (MOF), [Cu2(L1)∙5DMF]n (1) (H4L1 = 3,5-di(3,5-dicarboxyphenyl)nitrobenzene), has been designed, prepared and characterized. The single crystal X-ray diffraction results indicates that MOF 1 possess a 3D framework with 1D hexangular channels. The MOF 1 has been used as photocatalyst for the photodegradation of organic dyes viz. methyl violet (MV) and Rhodamine B (Rh B). The photocatalytic results indicated that 1 offered better photocatalysis towards the photodegradation of MV in comparison to Rh B. The probable mechanism for the photocatalytic activity of 1 has been addressed using density of states (DOS) and partial DOS calculations.
A Cu(II) based 3D MOF with 1D hexangular channels synthesized and its application as photocatalyst to degrade organic dyes explored. [Display omitted]
•The Cu(II)-based 3D MOF with 1D hexangular channels synthesized.•The MOF had been used as photocatalyst for the degradation of organic dyes.•MOF displays good recyclability to be used as a photocatalyst.•The DOS calculations have been used to assess the photocatalytic mechanism. |
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ISSN: | 1387-7003 1879-0259 |
DOI: | 10.1016/j.inoche.2018.12.025 |