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Effective personal protection is crucial for controlling infectious disease spread. However, commonly used personal protective materials such as disposable masks lack antibacterial/antiviral function and may lead to cross infection. Herein, a polyethylene glycol-assisted solvent-free strategy is proposed to rapidly synthesize a series of the donor-acceptor metal-covalent organic frameworks (MCOFs) (i.e., GZHMU-2, JNM-1, and JNM-2) under air atmosphere and henceforth extend it via in situ hot-pressing process to prepare MCOFs based films with photocatalytic disinfect ability. Best of them, the newly designed GZHMU-2 has a wide absorption spectrum (200 to 1500 nm) and can efficiently produce reactive oxygen species under sunlight irradiation, achieving excellent photocatalytic disinfection performance. After in situ hot-pressing as a film material, the obtained GZHMU-2/NMF can effectively kill E. coli (99.99%), S. aureus (99%), and H1N1 (92.5%), meanwhile possessing good reusability. Noteworthy, the long-term use of a GZHMU-2/NWF-based mask has verified no damage to the living body by measuring the expression of mouse blood routine, lung tissue, and inflammatory factors at the in-vivo level., (© 2023 Wiley‐VCH GmbH.)

Chemodynamic therapy (CDT) has emerged as a promising approach to cancer treatment, which can break the intracellular redox state balance and result in severe oxidative damage to biomolecules and organelles with the advantages of being less dependent on external stimulation, having deep tissue-healing abilities, and being resistant to drug resistance. There is considerable interest in developing CDT drugs with high efficiency and low toxicity. In this study, a new guanidinium-based biological metal covalent organic framework (Bio-MCOF), GZHMU-1@Mo, is rationally designed and synthesized as a multifunctional nanocatalyst in tumor cells for enhanced CDT. The DFT calculation and experimental results showed that due to the ability of MoO 4 2- ion to promote electron transfer and increase the redox active site, Cu 3 clusters and MoO 4 2- ions in GZHMU-1@Mo can synergistically catalyze the production of reactive oxygen species (ROS) from oxygen and H 2 O 2 in tumor cells, as well as degrade intracellular reducing substances, GSH and NADH, so as to disrupt the redox balance in tumor cells. Moreover, GZHMU-1@Mo exhibits a potent killing effect on tumor cells under both normal oxygen and anaerobic conditions. Further in vitro and in vivo antiproliferation studies revealed that the GZHMU-1@Mo nanoagent displays a remarkable antiproliferation effect and effectively inhibits tumor growth. Taken together, our study provides an insightful reference benchmark for the rational design of Bio-MCOF-based nanoagents with efficient CDT.

The anhydrous proton conductivity of Im@IEF-11 resulting from the integration of imidazole and porous IEF-11 has been investigated, and the highest proton conductive value can reach up to 7.64 × 10 -2 S cm -1 . Furthermore, IEF-11 is also developed to reduce CO 2 due to its reasonable structure and suitable energy band, and its CO formation rate is 31.86 μmol g -1 h -1 .

Due to the low vapor pressure of aniline, it is challenging to develop a specific rapid fluorescence detection material for low concentrations of aniline gas, which is suspected to result in carcinogenicity when people are exposed by ingestion, inhalation, and skin contact. Herein, the easy-preparing Schiff base ligands were employed to construct the binuclear cadmium(II) compounds featuring a good plane and fine luminescent property, and then, the end groups were changed, making the compounds metalloligands to further build the 3D metal-organic frameworks (MOFs), named MECS-2 . It is found that MECS-2 can achieve specific luminescent enhancement response for aniline gas. Furthermore, a large-scale MECS-2a film could be easily prepared by electrospinning nano MECS-2 , which presents the highly efficient and visual detection for aniline gas with the luminescent enhancement effect up to 20 times and good repeatability. Our work provides a good example for the efficient construction of MOF-based films with the fluorescence detection function for organic aromatic gases.

In this study, a novel polyoxometalates-based metal-organic frameworks (POMOFs) microsphere, that is [Ni(phen)H2O]·V2O6 (phen is o-phenanthroline), have been successfully fabricated by one-pot simple hydro(solvent)thermal reaction through regulating different solvent ratios (H2O/EtOH). The experimental results show that the solvent effect has a significant effect on the micro-morphology and the catalytic activity of the materials. The dual-function in electrocatalytic hydrogen evolution and catalytic reduction of Cr6+ of the as-prepared POMOFs microspheres have been also studied. The POMOF(V,Ni)_3 catalyst prepared in the medium of pure ethanol have the best catalytic activity, in which the overpotential of 159 mV for the electrode is comparable to that of MoS2-based electrode material, and the rate constant k reaches 0.14 in the process of catalytic reduction of Cr6+. In this study, a novel polyoxometalates-based metal-organic frameworks (POMOFs) microsphere [Ni(phen)H2O]·V2O6 have been successfully fabricated by one-pot simple hydro(solvent)thermal reaction through regulating different solvent ratios. The dual-function in electrocatalytic hydrogen evolution and catalytic reduction of Cr6+ of the as-prepared sample have been also studied. [ABSTRACT FROM AUTHOR]

The anhydrous proton conductivity of Im@IEF-11 resulting from the integration of imidazole and porous IEF-11 has been investigated, and the highest proton conductive value can reach up to 7.64 × 10−2 S cm−1. Furthermore, IEF-11 is also developed to reduce CO2 due to its reasonable structure and suitable energy band, and its CO formation rate is 31.86 μmol g−1 h−1. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) provide an ideal platform for loading various guests owing to their available space, and can be developed as a class of multifunctional materials. Herein, we cover the design and synthesis of two kinds of exchanged frameworks with multifunctional applications based on H3ImDC and In(NO3)3·2H2O through guest exchange inside the framework. The guest ammonium ion (NH4+) and [Ru(2,2′-bipyridine)3]2+ (Rubpy) are selected to exchange the dimethylammonium cation (Me2NH2+) encapsulated within In-MOF, giving birth to two kinds of new MOFs, named NH4+@In-MOF and Rubpy@In-MOF respectively. The proton conduction of NH4+@In-MOF and the CO2 photoreduction of Rubpy@In-MOF are investigated. Under different test conditions, the proton conductive behaviors of NH4+@In-MOF are evaluated and the best proton conductive value can reach up to 9.81 × 10−3 S cm−1. Compared to the original In-MOF, Rubpy@In-MOF exhibits a significantly enhanced CO2 photoreduction performance under a pure CO2 atmosphere. Furthermore, its photocatalytic activity is retained even under a 10% CO2 gas atmosphere, displaying a synergistic effect between Rubpy and In-MOF24 within Rubpy@In-MOF. [ABSTRACT FROM AUTHOR]

In this study, a novel polyoxometalates-based metal-organic frameworks (POMOFs) microsphere, that is [Ni(phen)H2O]·V2O6 (phen is o-phenanthroline), have been successfully fabricated by one-pot simple hydro(solvent)thermal reaction through regulating different solvent ratios (H2O/EtOH). The experimental results show that the solvent effect has a significant effect on the micro-morphology and the catalytic activity of the materials. The dual-function in electrocatalytic hydrogen evolution and catalytic reduction of Cr6+ of the as-prepared POMOFs microspheres have been also studied. The POMOF(V,Ni)_3 catalyst prepared in the medium of pure ethanol have the best catalytic activity, in which the overpotential of 159 mV for the electrode is comparable to that of MoS2-based electrode material, and the rate constant k reaches 0.14 in the process of catalytic reduction of Cr6+. In this study, a novel polyoxometalates-based metal-organic frameworks (POMOFs) microsphere [Ni(phen)H2O]·V2O6 have been successfully fabricated by one-pot simple hydro(solvent)thermal reaction through regulating different solvent ratios. The dual-function in electrocatalytic hydrogen evolution and catalytic reduction of Cr6+ of the as-prepared sample have been also studied. [ABSTRACT FROM AUTHOR]

[Display omitted] • ZIF-90 nanoparticles with different particle sizes were synthesized. • pH- and α-amylase-responsive nanocarriers were successfully prepared. • β-CD-NH 2 surface coating reduced the photodegradation of indoxacarb. • IDC@ZIF-90-CD was able to disrupt the intestinal cells of red imported fire ants. • IDC@ZIF-90-CD affected amino acid metabolic pathways in red imported fire ants. The invasion area of red imported fire ants (RIFAs) in China continues to expand due to factors such as ecological changes and human activities, and the resulting damage is becoming increasingly severe. The development of smart nanopesticides that respond to environmental stimuli response with precisely controlled release has great potential in improving insecticidal effects. In this work, a smart pH and α-amylase dual stimuli-responsive pesticide delivery system was constructed by combining mono-(6-amino-6-deoxy)-β-cyclodextrin (β-CD-NH 2) with zeolitic imidazole skeleton-90 (ZIF-90) nanoparticles (IDC@ZIF-90-CD) loaded with indoxacarb. The average particle size of the prepared IDC@ZIF-90-CD was 249 nm, and the loading efficiency was 18.43%. The β-CD-NH 2 coating on the surface of nanoparticles reduced the photodegradation of indoxacarb and prevented the premature release of the active ingredient. In vitro release kinetics showed that IDC@ZIF-90-CD rapidly released IDC under acidic and amylase conditions, consistent with the oral and intestinal environment of RIFAs. The results of bioactivity tests showed that IDC@ZIF-90-CD enhanced the toxicity of IDC toward RIFAs by increasing feeding and damaging intestinal cells. The mortality rate of the IDC@ZIF-90-CD-treated group was significantly higher than that of the IDC EC-treated group at 72 h. The nontargeted metabolomic results showed that IDC@ZIF-90-CD affected the metabolism of RIFAs by interfering with the metabolic pathways of six amino acids and one amino acid transport carrier, whereas IDC EC interfered with only two of these amino acid metabolic pathways. Overall, this work provides insight into the effective control of RIFA damage for sustainable pest management. [ABSTRACT FROM AUTHOR]