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SOLID STATE SCIENCES · 2023 · IF 3.5

Synthesis, structure and characterization of new compounds HA5M6(OH)4F4(HPO4)8 (A = K, Rb; M = Fe, Ga)

Ningxia Li,Qi Luo,Meiyan Cui,Zhiying Zhao,Zhangzhen He

New fluorophosphate compounds H A 5 M 6 (OH) 4 F 4 (HPO 4 ) 8 ( A  = K, Rb; M  = Fe, Ga) were synthesized by a fluorine-rich hydrothermal method . These compounds crystallize in the monoclinic system with a P2 1 /n space group, exhibiting an open framework structure built by [PO 3 (OH)] groups, [MO 4 (OH)F], and [MO 4 F 2 ] octahedra, where ten-membered-ring channels, eight-membered-ring channels, six-membered-ring channels, and the linear M 3+ trimers are seen. The characterizations were carried out by powder XRD , EDS , FT-IR spectra, and magnetic measurements. The results confirmed that H A 5 Fe 6 (OH) 4 F 4 (HPO 4 ) 8 ( A  = K, Rb) show a quite similar magnetic behavior, possessing an antiferromagnetic ordering at 14.7 K and 15.6 K, respectively. The changes of the magnetic entropy for such antiferromagnetic orderings can be estimated as ∼10.7 J mol −1  K −1 and ∼13.4 J mol −1  K −1 .

✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Photocatalytic conversion of nitrogen to ammonia with water on triphase interfaces of hydrophilic-hydrophobic composite Bi4O5Br2/ZIF-8

Jianxin Liu,Rui Li,Xiang Zu,Xiaochao Zhang,Yunfang Wang,Yawen Wang,Caimei Fan

Photocatalysis can produce NH 3 using N 2 and H 2 O at room temperature and atmospheric pressure, which has been considering as a safe, clean, and sustainable NH 3 synthesis. However, the poor solubility and slow diffusion rate of N 2 in water severely limited the nitrogen activation efficiency. Herein, we solve this problem by developing a hydrophilic-hydrophobic structure photocatalyst with gas-liquid-solid triphase reaction interface, where hydrophilic Bi 4 O 5 Br 2 is deposited on the surface of hydrophobic ZIF-8 to form a novel Bi 4 O 5 Br 2 /ZIF-8 composite photocatalyst. Such triphase interface architecture allows the direct delivery of N 2 from gas phase to the photocatalytic reaction interface replaced the diffusion of N 2 through the liquid phase. This rapid supply of N 2 can efficiently capture photoinduced electrons, thereby promoting the utilization efficiency of photo-induced electrons and the nitrogen fixation activation. This novel Bi 4 O 5 Br 2 /ZIF-8(30%) composite photocatalyst with good triphase contact performance shows obviously improved photocatalytic   nitrogen   fixation activity 327.338 μmol·L −1 ·h −1 ·g −1 (3.6 times than that of Bi 4 O 5 Br 2 ). Furthermore, efficient molecular nitrogen activation by Bi 4 O 5 Br 2 /ZIF-8 further brings out an attractive potential to improve other gas-consumption reactions, such as CO 2 reduction, according to this concept of triphase direct contact.

✓ 已验证 DOI 高影响因子
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Nanoscale · 2018 ·Vol. 10 ·期 45 ·21284-21291 · IF 7.233

Facile synthesis of Ni11(HPO3)8(OH)6/rGO nanorods with enhanced electrochemical performance for aluminum-ion batteries

Jiguo Tu,Haiping Lei,Mingyong Wang,Zhijing Yu,Shuqiang Jiao

The electrochemical behaviors of the ultrashort nickel phosphite nanorods supported on reduced graphene oxide (Ni11(HPO3)8(OH)6/rGO nanorods), as a candidate for cathodic applications in aluminum-ion batteries, are firstly investigated. Ni11(HPO3)8(OH)6/rGO nanorods are synthesized by a facile solvothermal process. Ni11(HPO3)8(OH)6 and Ni11(HPO3)8(OH)6/rGO cathodes both possess very high initial discharge capacities of 132.4 and 182.0 mA h g−1 at a current density of 200 mA g−1, respectively. In addition, the long-term cycling stability of the Ni11(HPO3)8(OH)6/rGO cathode is further evaluated, exhibiting a discharge capacity of 49.2 mA h g−1 even over 1500 cycles. More importantly, the redox reaction mechanism of the Ni11(HPO3)8(OH)6 cathode for aluminum-ion batteries revealed that Ni11(HPO3)8(OH)6 is partially substituted with Al3+ to form AlmNin(HPO3)8(OH)6 and metallic Ni in the nanorod-like Ni11(HPO3)8(OH)6 cathodes during the discharge process. These findings are of great significance for the further development of novel materials for aluminum-ion batteries.

✓ 已验证 DOI 高影响因子
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Journal of Water Process Engineering · 2022 · IF 7.34

Enhanced visible-light photocatalytic performance of ZIF-8-derived ZnO/TiO2 nano-burst-tube by solvothermal system adjustment

Qiushi Jiang,Zhaolian Han,Yinjie Qian,Yafeng Yuan,Yating Ren,Mingyu Wang,Zhiqiang Cheng

A novel strategy for the preparation of heterojunction derivants by regulating the loading of precursors was proposed and applied for the first time to effectively remove dyes and antibiotics. Zeolite imidazole framework-8 (ZIF-8)-derived ZnO/TiO 2 nano-burst-tube (NBT) was prepared by calcination of ZIF-8 as precursor grown in a solvothermal system adjusted by NH 4 OH or NaOH , TiO 2 NBT as solvothermal substrate. Through a reasonable selection of solvothermal system, ZIF-8-derived ZnO/TiO 2 NBT not only provides enhanced specific surface area (1012.3 m 2 /g), but also enhances the visible light response and charge separation of TiO 2 NBT, whose instantaneous photocurrent density is up to 53 mA cm −2 , which is three times that of TiO 2 NBT. Under visible light irradiation, ZnO/TiO 2 NBT achieved rapid degradation of Rhodamine B(RhB), tetracycline hydrochloride (TCH) and chlortetracycline hydrochloride (CTC) with complete removal within 20 min, outperforming ZnO, ZIF-8, TiO 2 NBT and ZIF-8/TiO 2 NBT, with excellent cyclic photocatalytic performance. The results show that the degradation pathways of RhB, TCH and CTC are different. The work provides a promising strategy for multifunctional derivative photocatalytic materials preparation.

✓ 已验证 DOI 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2015 · IF 3.091

Highly hydrogen-permselective zeolitic imidazolate framework ZIF-8 membranes prepared on coarse and macroporous tubes through repeated synthesis

Yaqiong Zhu,Qian Liu,Jürgen Caro,Aisheng Huang

Highly hydrogen-permselective zeolitic imidazolate framework ZIF-8 membranes are prepared on coarse and macroporous Al 2 O 3 tubes through a repeated synthesis strategy for the separation of H 2 /CO 2, H 2 /CH 4 , and H 2 /C 3 H 8 mixtures. Since the amino-groups of 3-aminopropyltriethoxysilane (APTES) can coordinate to the free Zn 2+ centers and thus bind the growing nano-crystals directly, the nucleation and growth of well intergrown ZIF-8 membranes could be promoted through a repeated synthesis of the ZIF-8 layer on APTES-modified macroporous Al 2 O 3 tubes. The SEM and XRD characterizations indicate that a dense and phase-pure ZIF-8 membrane with a thickness of about 25.0   μm can be formed on the alumina tubes by microwave synthesis at 105   °C for 3   h, and no cracks, pinholes or other defects were observed in the membrane layer. The ZIF-8 membranes were evaluated in single gas permeation and mixed gas separation. Attributed to the preferential adsorption affinity and capacity as well as a highly porous structure with nano-sized channels, the ZIF-8 membrane displays a high hydrogen permselectivity. For the separation of equimolar H 2 /CO 2 , H 2 /CH 4 , H 2 /C 3 H 8 mixtures at 100   °C and 2   bar, the mixture separation factors of H 2 /CO 2 , H 2 /CH 4 , and H 2 /C 3 H 8 are 5.6, 44.0, 328.6, with a H 2 permeance of about 1.1   ×   10 −7   mol   m −2   s −1   Pa −1 , which is promising for potential applications in hydrogen purification and separation.

✓ 已验证 DOI 高影响因子
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JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS · 2025 · IF 6.2

Utilizing the self-stabilizing stage of ZIF-8 for highly efficient in situ Cl capture during PVC pyrolysis

Chenhao Li,Yi Niu,Linlin Yi,Yaoqiang Li,Jia Fu,Fang Tang,Kaiyuan Li,Yanyan Zou

This paper explores the application of zeolitic imidazolate framework-8 (ZIF-8) in pyrolytic disposal of poly(vinyl chloride) (PVC), with the goal of assessing the in situ catalytic removal and capture effect of ZIF-8 on Cl, elucidating the migration pattern of Cl, revealing the mechanism of in situ Cl capture by ZIF-8. The results demonstrate that excellent catalytic and Cl trapping properties are exhibited by ZIF-8, and an additional 311.1 mg/g of organic Cl from PVC is facilitated to be removed at 250 ºC. The catalytic effect enhances Cl trapping at low temperatures. The solid-solid reaction between PVC and ZIF-8 during in situ pyrolysis significantly improves Cl capture compared to ex situ pyrolysis. During in situ pyrolysis, ZIF-8 shows excellent Cl capture between 250 and 350 ºC, where Cl is primarily captured in the solid phase as inorganic Cl. ZIF-8 achieves optimal Cl capture at 300 ºC, reaching a peak HCl removal rate of 89.5 %. At this temperature, the content of solid-phase inorganic Cl reaches a maximum of 442.0 mg/g, accounting for 78.7 wt% of the total Cl content. The key to Cl capture lies in the chemical adsorption sites of Zn²⁺ and organic ligands in the ZIF-8 structure, which can react with Cl in both solid-solid and gas-solid reactions. Additionally, crystals formed during pyrolysis create an adsorption barrier, ultimately enabling efficient Cl capture.

✓ 已验证 DOI 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Insight into the molecular mechanism of organic pollutants’ adsorption on magnetic ZIF-8 synthesized via a transformational route

Zhang Liu,C. Marquina,Wei Han,Joseph K.C. Kwan,M. Ricardo Ibarra,King Lun Yeung

This study presents the synthesis of Fe 3 O 4 @Zeolite Imidazolate Framework-8 (Fe 3 O 4 @ZIF-8), a novel magnetic core–shell adsorbent engineered for enhance adsorption of organic pollutants. The process begins with the formation of spherical magnetite aggregates (i.e., Fe 3 O 4 ) via a solvothermal method, using polyacrylic acid for stabilization and capping. A ZIF-8 shell is then grown through a sol gel process followed by reaction with 2-methylimidazole, resulting in a crystalline shell approximately 60 nm thick. Characterization techniques, including energy dispersive X-ray analysis and X-ray diffraction, confirm the successful preparation of Fe 3 O 4 @ZIF-8. The adsorption capabilities were evaluated using methylene blue (MB) and diclofenac sodium (DCF) as model pollutants. Fe 3 O 4 @ZIF-8 demonstrated rapid removal efficiencies, with 98 % removal of MB (6.01 × 10 -4 mg·g −1 ·min −1 ) and DCF (4.43 × 10 -4 g·mg −1 .min −1 ) within 15 and 30 min, respectively, significantly outperforming conventional activated carbon. Thermodynamic studies indicate that the adsorption processes are spontaneous; enthalpic changes drive MB adsorption, while DCF is influenced by entropic factors. Molecular modeling reveals preferential adsorption behaviors on different ZIF-8 facets, with stronger interactions for MB due to π-π stacking and hydrogen bonding. These findings underscore the potential of Fe 3 O 4 @ZIF-8 as an effective adsorbent for water purification, highlighting its substantial adsorption capacity (73.2 mg·g −1 for MB and 53.8 mg·g −1 for DCF), stability, and reusability.

✓ 已验证 DOI 高影响因子
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2025 · IF 6.2

Crystal Structure of Autophagy-Associated Protein 8 at 1.36 Å Resolution and Its Inhibitory Interactions with Indole Analogs

Shanqi Zhang,Xin Luo,Xiu Yuan,Danxia Wu,Jing Liu,Kunhong Zhao,Youwei Xu,Jingjiang Zhou,Xiangyang Li,Qing X. Li

Autophagy-associated protein 8 (ATG8) is essential for autophagy and organismal growth and development. In this study, we successfully resolved the crystal structure of Drosophila melanogaster (D. melanogaster) ATG8a (DmATG8a) at 1.36 Å resolution. Being distinct from previously characterized ATG8 homologues, DmATG8a (121 residues) adopts a unique fold comprising five α-helices and four β-folding strands, in contrast to the canonical four α-helices and four β-folding strands observed in other ATG8 proteins. DmATG8a features two active cavities: hydrophobic pocket 1 (HP1) and hydrophobic pocket 2 (HP2), which are essential for the normal physiological function of ATG8. Indole and its analogs can bind specifically with HP1. Microscale thermophoresis results demonstrated a strong affinity of 6-fluoroindole with DmATG8a (3.54 μmol/L), but no affinity with the DmATG8aK48A mutant, suggesting that Lys48 is critical in binding 6-fluoroindole probably via a hydrogen bond interaction. The half-maximum lethal concentration (LC50) of 6-fluoroindole against D. melanogaster adult flies was 169 μg/mL. Our findings establish DmATG8a as a promising target for developing indole-based insecticides.

✓ 已验证 DOI PubMed 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Multifunctional Ac@ZIF-8/AgNPs nanoplatform with pH-responsive and ROS scavenging antibacterial properties promotes infected wound healing

Yipeng Pang,Maofang Zhao,Yuhan Xie,Yanping Wang,Yuxin You,Yongding Ke,Chaoyi Zhang,Xiaohan Chen,Yijia Yang,Chunlei Zhang,Xi Chen,Yi Liu,Xingtang Fang

The development of non-antibiotic strategies for combating bacterial infections, particularly through reactive oxygen species (ROS) accumulation accompanying inflammation, has attracted much attention. Despite Allicin (Ac) emerges as a promising antimicrobial agent with wide and remarkable bioactivity, it still displays quite limited ROS scavenging and anti-inflammation capacity due to uncontrolled and poor bioavailability. Herein, a multifunctional nanoplatform with pH-dependent and ROS-scavenging antibacterial, anti-inflammatory and proangiogenic properties is introduced to promote infected wound healing by integrating Ac into silver nanoparticles (AgNPs)-loaded zeolite imidazole framework (ZIF-8), namely Ac@ZIF-8/AgNPs. Primarily, the nanoplatform is activated and controlled release in the infection microenvironment, with disrupting biofilms, scavenging ROS and antibacterial capacitys, outperforming conventional Ac. Moreover, in the mouse models induced by bacterial infection, Ac@ZIF-8/AgNPs can alleviate the inflammatory condition, scavenge ROS, facilitate the regeneration of collagen fiber and enhance vascular formation, collectively accelerating wound healing. Overall, this biocompatible nanoplatform is provided as a reliable approach to solve the long-standing problem of infected wound healing.

✓ 已验证 DOI 高影响因子
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BIOORGANIC & MEDICINAL CHEMISTRY · 2025 · IF 3

Design, synthesis and biological activity of 8-hydroxy modified urolithin A derivatives as phosphodiesterase type II (PDE2) inhibitors

Feng Zhou,Xiaoqing Feng,Zhongqiu Xu,Fen Yan,Guoqiang Song,Long Tang

Urolithin A (UA) is a naturally occurring polyphenolic compound.Due to its remarkable efficacy in safeguarding the central nervous system, UA has emerged as a promising candidate for drug development targeting neurodegenerative diseases such as Alzheimer’s. However, the source of UA is limited and the activity of UA to inhibit PDE2 needs to be further improved. Therefore, this study will be optimized on the basis of UA to seek PDE2 inhibitors with better activity. In this study, we designed a series of UA derivatives based on 4HTX as the target protein and UA as the lead compound, utilizing the binding crystal structures of 4HTX and BAY60-7550 as references. After thorough screening, we successfully identified the 8-hydroxyl group as the precise site of modification. Utilizing 2-bromo-5-hydroxybenzoic acid as our primary raw material, we synthesized a series of the 8-hydroxyl modified UA. Subsequently, we evaluated the inhibitory activity of these synthesized UA derivatives using a phosphodiesterase assay kit. Ultimately, we screened a total of 34 derivatives; among them, compounds 1f, 1q, 2d, and 2j exhibited significant inhibitory activity against PDE2 with half-maximal inhibitory concentrations of 3.05 μM,0.67 μM, 0.57 μM, and 4.96 μM, respectively.

CAS / MDL: 630-93-3
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Carbon Letters · 2025 · IF 5.8

MnMgFe-LDHs/ZIF-8/B, N-WMCNTs nanocomposites for efficient electrochemical detection of nitrite and heavy metal ions

Du Xue,Han Tong,Jin Biao,Meng Long-Yue,Han Lian-Hua

Contamination of food with heavy metal ions and nitrites poses a serious threat to human health. Consequently, the development of fast and sensitive platforms for detecting these contaminants is urgently required. In this paper, a novel MnMgFe-LDHs/DC sensor is constructed based on a simple strategy, in which MnMgFe layered double hydroxide (LDHs) is used as a metal precursor, and a unique "island bridge" carbon network structure is generated by its pyrolysis with ZIF-8@B, N-WMCNTs. The electrical conductivity was enhanced, and a large electroactive surface area was provided for the MnMgFe-LDHs/DC. The electrochemical properties of Pb 2+ , Cd 2+ and nitrite were investigated using this electrode as a working electrode. Under optimized conditions, the sensing platform exhibited a wide linear range with the Pb 2+ , Cd 2+ , and NO 2 − limits of detection of 46.16 nM, 59.25 nM, and 0.083 μM, respectively. Of particular note is that this sensing platform exhibits outstanding anti-interference capabilities. It can precisely and efficiently conduct the detection of nitrite and heavy metal ions in pickled foods.

✓ 已验证 DOI 高影响因子
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JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY · 2025 · IF 4.9

Formulation of pH-sensitive ZIF-8 (MOF) impregnated amino-chitosan biocomposite beads for sustained release of 5-fluorouracil

Ahmed M. Omer,Eman M. Abd El-Monaem,Heba S. Hassan,Mahmoud A. Elmeligy,Angela Kleinová,Abdelazeem S. Eltaweil,Abolfazl Heydari

pH-sensitive carriers have emerged as an optimal choice for the oral administration of anticancer drugs, exhibiting the desired release performance. This study aims to develop biocomposite beads for the sustained release of the anticancer drug 5-fluorouracil (5-FU). Here, 5-FU was encapsulated within a ZIF-8 metal-organic framework (MOF), which was subsequently impregnated into amino-chitosan beads. The resulting Am-CS@ZIF-8 biocomposite beads were characterized for their chemical structure, surface morphology, elemental composition, crystallinity, surface charges, and mechanical properties utilizing Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), zeta potential analysis, and a texture analyzer, respectively. The developed beads exhibited a textured surface, denser composition, and a positively charged surface with a maximum zeta potential of +12.4 at pH 7.4. In comparison to Am-CS beads, the Am-CS@ZIF-8 biocomposite beads demonstrated superior mechanical properties, achieving a maximum stress value of 5.668 MPa compared to the 1.874 MPa recorded for pure Am-CS beads. pH sensitivity was assessed through the investigation of water uptake behavior at pH 1.2 and pH 7.4. The Am-CS@ZIF-8 biocomposite beads demonstrated a high encapsulation efficiency of approximately 81.6 % for 5-FU. They exhibited pH-responsive release behavior, with only 17 % of the drug released at pH 1.2 after 2 h and a sustained release of 52 % at pH 7.4 over 24 h. The release mechanism was predominantly governed by Fickian diffusion, as closely fitted by the Peppas-Sahlin kinetic model. The formulated carrier confirmed its biodegradability under enzymatic physiological conditions, suggesting its potential applicability as an effective system for the oral delivery of anticancer drugs.

CAS / MDL: 10196-18-6 693-98-1
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