Visible-Light-Responsive Polyoxometalate-Based Metal-Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulant.

Inorg Chem

Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences, Henan University, Kaifeng, Henan 475004, P. R. China.

Published: August 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Two [Ru(bpy)] derivative-incorporated polyoxometalate-based metal-organic frameworks (POM@MOFs), {Cd(HO)Mn(HO)[Ru(dcbpy)][PMoMoO]}·6HO () and {Cd(HO)Cu(HO)[Ru(dcbpy)][PMoMoO]}·6HO (), have been prepared through a conventional hydrothermal method. The introduction of Ru metalloligands enhanced the visible light absorption of POM@MOFs, and the photocatalytic detoxification reaction of mustard gas simulant 2-chloroethyl ethyl sulfide (CEES) confirmed their fascinating photocatalytic performances. Under visible light irradiation (λ > 400 nm), both and exhibited efficient photocatalytic properties for the detoxification of CEES into nontoxic CEESO in air, with a selectivity of 97% and a TOF of 26.6 min. Besides, also exhibited commendable reusability and stability after three reaction cycles. In addition, EPR measurements and radical scavenging experiments were carried out to verify the generation of O and O, presenting reliable evidence for the detoxification mechanism.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.inorgchem.5c03166DOI Listing

Publication Analysis

Top Keywords

polyoxometalate-based metal-organic
8
metal-organic frameworks
8
photocatalytic detoxification
8
mustard gas
8
gas simulant
8
visible light
8
visible-light-responsive polyoxometalate-based
4
photocatalytic
4
frameworks photocatalytic
4
detoxification
4

Similar Publications

Visible-Light-Responsive Polyoxometalate-Based Metal-Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulant.

Inorg Chem

August 2025

Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences, Henan University, Kaifeng, Henan 475004, P. R. China.

Two [Ru(bpy)] derivative-incorporated polyoxometalate-based metal-organic frameworks (POM@MOFs), {Cd(HO)Mn(HO)[Ru(dcbpy)][PMoMoO]}·6HO () and {Cd(HO)Cu(HO)[Ru(dcbpy)][PMoMoO]}·6HO (), have been prepared through a conventional hydrothermal method. The introduction of Ru metalloligands enhanced the visible light absorption of POM@MOFs, and the photocatalytic detoxification reaction of mustard gas simulant 2-chloroethyl ethyl sulfide (CEES) confirmed their fascinating photocatalytic performances. Under visible light irradiation (λ > 400 nm), both and exhibited efficient photocatalytic properties for the detoxification of CEES into nontoxic CEESO in air, with a selectivity of 97% and a TOF of 26.

View Article and Find Full Text PDF

The selective oxidation of benzylic C-H bonds to C═O bonds is an economical strategy to produce aromatic ketones and aldehydes directly. However, the activation of C-H bonds is challenging due to their high bond energy. In this work, two isostructural three-dimensional (3D) Wells-Dawson-type polyoxometalate (POM)-based metal-organic complexes (POMOCs), [Cu(L)(PMoO)(HO)]·16HO () and [Cu(L)(PWO)(HO)]·14HO () (L = ,'-(ethane-1,2-diyl)bis(pyrazine-2-carboxamide)) were synthesized through the self-assembly of Wells-Dawson-type POMs with Cu and a flexible dipyrazine-dicarboxamide ligand L under hydrothermal conditions, which were structurally characterized by infrared spectroscopy (IR) and powder X-ray diffraction (PXRD).

View Article and Find Full Text PDF

The critical role of chirality in biological and chemical systems has driven the demand for advanced nanocatalytic platforms capable of achieving efficient chiral selective recognition and conversion. The present study details the design of chiral polyoxometalate metal-organic frameworks (POMOFs) based on polyoxometalates, which mimic enzyme-catalyzed multiphase catalysis by combining the redox activity of Keggin-type polyoxometalates with the stereoselectivity of chiral MOFs. This design strategy precludes the aggregation of catalytic sites through uniformly dispersed POM clusters.

View Article and Find Full Text PDF

Interlayer Confinement Strategy in Two-Dimensional Polyoxometalate-Based Metal-Organic Frameworks for Enhancing Proton Conduction.

ACS Appl Mater Interfaces

August 2025

School of Chemistry and Environmental Engineering; Jilin Provincial Science and Technology Innovation Center of Optical Materials and Chemistry; Jilin Provincial International Joint Research Center of Photo-functional Materials and Chemistry, Changchun University of Science and Technology, Changchun

Proton exchange membranes are crucial components in electrochemical energy devices. Nevertheless, the development of high-performance proton-conducting materials remains a considerable challenge, primarily due to the inherent difficulty in constructing dense and continuous hydrogen-bonding networks under ambient conditions. To overcome this limitation, the intentional incorporation of short hydrogen bonds has been applied as a critical design strategy and plays a critical role in enabling efficient proton transport.

View Article and Find Full Text PDF

Releasing the Guest Molecules in 2D Polyoxometalate-Based Metal-Organic Frameworks for Enhancing Proton Conductivity and Iodine Capturing.

Inorg Chem

June 2025

Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education, College of Chemistry, Northeast Normal University, Changchun, Jilin 130024, China.

Crystalline 2D polyoxometalate-based metal-organic frameworks (PMOFs) provide platforms for discussing structure-property relationships. However, properties regulated by releasing guest molecules in 2D PMOFs have rarely been reported. Herein, we fabricated two 2D PMOFs, [TBA][-HPMoMoOZn(BTC)(IM)]·IM (, TBA = tetrabutylammonium ion, HBTC = 1,3,5-benzenetricarboxylic acid, IM = imidazole) and [TBA][-HPMoMoOZn(BTC)(BPE)] (, BPE = 1,2-bis(4-pyridyl) ethylene), where the interlayer regions were occupied by large-sized TBA guests and dangled IM/BPE ligands.

View Article and Find Full Text PDF