JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2025
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IF 9.7
Shihua Wang,Yiting Qiu,Lichao Yu,Kongqin Lu,Bing Du,Jin Zhang,Hangxin Gong,Aocheng Ren,Min Chen,Hongchen Zhang,Xu-Feng Zang,Xiaoxia Ye,Leyi Cai,Yun-Yun Quan,Zu-Sheng Huang
The precise distribution and subcellular localization of photosensitizers (PSs) play a crucial role in maximizing the utilization of reactive oxygen species (ROS) and enhancing photodynamic therapy (PDT). However, the therapeutic efficacy of PDT is significantly compromised by the hypoxic microenvironment, particularly in malignant tumors. To address these challenges, we designed and synthesized three donor–donor-π-bridge-acceptor (D-D-π-A) type aggregation-induced emission (AIE) PSs: TCM-OTs , TCM-OH , and TCPy-OH . By fine-tuning the acceptor and donor substituents, we successfully modulated organelle-targeting specificity and ROS generation to mitigate hypoxia-related limitations. Among these compounds, TCM-OH emerged as a highly promising PS, exhibiting selective mitochondrial targeting and efficient type-I ROS generation. To further enhance its pharmacological properties, we encapsulated each PS into DSPE-PEG2k to form nanoparticles (NPs). Notably, TCM-OH NPs facilitated the production of superoxide (•O 2 − ) and hydroxyl radicals (•OH) within mitochondria, leading to mitochondrial dysfunction and subsequent cell death via a synergistic ferroptosis-apoptosis pathway under light irradiation. Both in vitro and in vivo experiments demonstrated the potent therapeutic efficacy of this strategy, with minimal toxicity, underscoring its potential for hypoxic cancer treatment. Overall, this study provides a rational design framework for developing potent type-I PSs with multimodal capabilities for biomedical applications.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Mingxian Duan,Yeshuang Wang,Huiling Fan,Zhelin Su,Chao Yang,Jiawei Kou,Ju Shangguan
Thiophene (C 4 H 4 S) removal from coke oven gas is critical to its subsequent high valuable utilization but remains a challenge. MOF-199 was considered as a promising candidate for C 4 H 4 S adsorption removal owing to its nature of enriched opened Cu sites. However, the presence of mixed valence of Cu(II) and Cu(I) in MOF-199 makes it puzzling to their respective contribution to the removal of C 4 H 4 S. Herein, a series of MOF-199 with different Cu(I) contents were synthesized using different methods, including hydrothermal, solution diffusion, and ultrasonic, and their C 4 H 4 S adsorption performance were investigated. The respective contributions of Cu(II) and Cu(I) to the C 4 H 4 S removal was systematically discussed. The collected results indicated that although the samples prepared with different methods present a remarkable difference in textural characters, the latter was found to have a negligible influence on the C 4 H 4 S removal owing to MOF-199(H) affording an inferior surface area and pore volumes but performing the best C 4 H 4 S removal capacity of 53.7 mg S/g. The co-adsorption results of CH 3 SCH 3 and C 4 H 4 S indicated that the excellent performance of MOF-199(H) mainly attributed to the presence of Cu(I), which provides active sites for C 4 H 4 S adsorption through π complex coordination. Cu(II) species was also found to the C 4 H 4 S adsorption via soft-acid-base coordinated interaction, but its contribution is 8.3 mg S/g, only accounting for 15.5 %. Additionally, the adsorption of C 4 H 4 S on MOF-199(H) was found to follow the intra-particle diffusion model and the Langmuir models. Moreover, MOF-199(H) also exhibited an excellent regeneration performance due to the weak interaction between C 4 H 4 S and their opened Cu sites, the C 4 H 4 S adsorption capacity still reaches 50.6 mg S/g after three regeneration cycles, about 94 % of its initial value. The results collected in this study will provide new insights for the manipulation of performance of C 4 H 4 S adsorption on the MOF-199.
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CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Bin Zhang,Ziwen Han,Yanjun Xin,Yanjie Zhang,Wenqian Li,Boda Li,An Ding,Jun Ma,Xu He
Herein, vacuum ultraviolet (VUV) was introduced to enhance the activation rate of peroxymonosulfate (PMS) by copper ions for the first time. Compared with ultraviolet (UV), the redox cycle rate of Cu(II)/Cu(I) was prominently enhanced by VUV due to the combined driving effect of UV, hydrated electron and active hydrogen atoms. The accelerated Cu(II)/Cu(I) cycle in VUV/PMS/Cu(II) system led to 2.89 times higher degradation efficiency of 2,4-dichlorophenol (2,4-DCP) than that by UV/PMS/Cu(II) system. More importantly, the initial Cu(II) concentration (5 μM) in VUV/PMS/Cu(II) system was only 1/5 of the guideline value in WHO standards for drinking water, and the initial PMS concentration was also 1 order of magnitude lower than that in most PMS based systems for water treatment. Furthermore, the reaction mechanism and possible degradation pathways of 2,4-DCP were also proposed. This study verified the possibility for the utilization of trace Cu(II) in water to decompose refractory micro-pollutants by PMS activation.
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ADVANCED FUNCTIONAL MATERIALS
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2025
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IF 19
Ying-Ying Zhao,Hai-Yian Sun,Chang Wei,Tian-Yu Pan,Lu Yang,Mei-Ling Feng,Xiao-Ying Huang
The highly selective capture of 137 Cs + from complex solutions is still challenging because of its high solubility, easy mobility, and the influence of interfering ions. Here, a reliable strategy is demonstrated for specific Cs + ion recognition and separation through constructing the confined space as an “ion lock” in the microporous framework. A new 3D microporous indium oxalatophosphate with the highly selective Cs + capture, namely [Me 2 NH 2 ] 1.5 [In 2 (PO 4 ) 0.5 (H 2 PO 4 )(HPO 4 ) 1.5 (C 2 O 4 )] (FJSM-NINPC) is prepared. FJSM-NINPC with excellent radiation resistance shows ultra-fast kinetics (high removal rate of 97.63% within 1 min) and high adsorption capacity of 268.12 mg g −1 for Cs + . It can highly selectively capture Cs + under excessive competitive ions and even in environmental water samples. Furthermore, the ion exchange column filled with FJSM-NINPC can quickly separate and recover Cs + from mixed Cs + and Sr 2+ solution (separation factor SF Cs/Sr = 249.17). Moreover, single crystal structure analysis combined with density functional theory calculations confirms that Cs + ions are “encapsulated” in channels of FJSM-NINPC by the suitable spatial confinement and with strong Cs···O interactions. This work not only provides an unprecedented microporous metal oxalatophosphate with high Cs + selectivity but clearly reveals the Cs + capture mechanism and structure-function relationship of microporous materials for radionuclides remediation.
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ACS Applied Materials & Interfaces
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2021
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IF 9.229
Jian Zhao,Zhuo-Hao Jiao,Sheng-Li Hou,Yue Ma,Bin Zhao
Carboxylative cyclization of propargylic alcohols with CO2 is significant in synthetic chemistry, but harsh conditions are often needed according to reported results. Herein, a new stable nitro-functionalized metal–organic framework (MOF) of {[Co3(L)2(bpy)4(H2O)2]·DMF·H2O·bpy}n (1) was fabricated through the solvothermal reaction, which exhibited excellent stability in acid and basic solutions. Owing to the porous structure, unsaturated metal sites, and uncoordinated 4,4′-bpy ligands, 1 can serve as an excellent platform for catalytic applications. Hence, Ag(I) ions were incorporated in 1 through a postsynthetic method, and the as-synthesized Ag-1 catalyst with low metal loading (0.64 mol %) displayed excellent catalytic performance in the chemical fixation of CO2 with alkynols under room temperature and atmospheric pressure. The results of 1H NMR analyses further confirmed that Ag-1 can efficiently activate hydroxyl groups and promote the reaction. Moreover, the turnover frequency (TOF) of the Ag-1 catalyst can reach 262 h–1 in a short period of time, which is a high TOF value among the state-of-the-art MOF-based catalysts for catalyzing cycloaddition of CO2 with propargylic alcohols.
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FOOD CHEMISTRY
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2019
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IF 5.399
Qiumin Ye,Xiaohui Chen,Jing Yang,Datong Wu,Jianfeng Ma,Yong Kong
In this study, a sensitive and selective electrochemical sensing platform for the detection of Sudan I was developed with CuO nanoparticles-decorated 3D N -doped porous carbon (CuO/3DNPC). 3D N -doped porous carbon (3DNPC) was first prepared by calcining the precursors of 3D integrated polysaccharides, and then it was decorated with CuO nanoparticles by hydrothermal method. The CuO/3DNPC modified electrode showed high sensitivity and wide linear range for the detection of Sudan I due to the excellent electrocatalytic activity of CuO and the accelerated electron transfer by 3DNPC. In addition, the proposed CuO/3DNPC also exhibited high selectivity, high reproducibility and stability in the detection of Sudan I. Finally, the CuO/3DNPC based Sudan I sensor was applied in the detection of Sudan I in ketchup and chilli sauces, and the results demonstrated the potential of the developed CuO/3DNPC as a promising electrode material for accurate assay of Sudan I in food samples.
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ACS Biomaterials Science & Engineering
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2022
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IF 5.395
Wenyi Xia,Tao Yan,Lianlei Wen,Shijie Zhu,Wang Yin,Miao Zhu,Meidong Lang,Chunsheng Wang,Changfa Guo
Despite the fact that heart transplantation (HTx) is a relatively mature procedure, heart ischemic and reperfusion (I/R) injury during HTx remains a challenge. Even after a successful operation, the heart will be at risk of primary graft failure and mortality during the first year. In this study, temperature-sensitive polymer poly(N-n-propylacrylamide-co-N-tert-butyl acrylamide) (PNNTBA) was coated on diallyl trisulfide (DATS)-loaded mesoporous silica nanoparticles (DATS-MSN) to synthesize hypothermia-triggered hydrogen sulfide (H2S) releasing particles (HT-MSN). Because the PNNTBA shell dissolves in phosphate-buffered saline at 4 °C, the loaded DATS could continuously release H2S within 6 h when activated by glutathione (GSH). Furthermore, after co-culturing biocompatible HT-MSN with cardiomyocytes, H2S released from HT-MSN at 4 °C was found to protect cardiomyocytes from ischemic and reperfusion (I/R) injury. In detail, the rate of cell apoptosis and lactate dehydrogenase activity was decreased, as manifested by increased BCL-2 expression and decreased BAX expression. More importantly, in an isolated heart preservation experiment, HT-MSN demonstrated potent protection against cardiac I/R injury and reduced expression of inflammatory factors TNF-α and IL-1β. This study provided a new method for the controlled release of H2S by the donor and myocardial protection from I/R injury.
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ANALYTICAL CHEMISTRY
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2017
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IF 6.32
Jinyang Chen,Xinghu Ji,Zhike He
On the basis of an interesting experimental phenomenon, a novel and smart composite reagent consisting of double-stranded DNA-templated copper nanoparticles (dsDNA–CuNPs) and DNA intercalator (SYBR Green I) was developed and exploited for hydrogen peroxide (H2O2) detection as well as oxidase-based biosensing. The study found that, within the composite reagent, the small molecule SYBR Green I was easily adsorbed on the surfaces of CuNPs, instead of intercalating into the dsDNA. So the composite reagent only exhibited the red fluorescence generated from dsDNA–CuNPs. However, when the solution of H2O2 was added into the composite reagent, the CuNPs were deconstructed and their fluorescence was quenched; meanwhile, the inhibition of SYBR Green I binding with dsDNA was eliminated. As a result, the mixed solution of the composite reagent with H2O2 exhibited green fluorescence generated from the intercalation of SYBR Green I into dsDNA. Since H2O2 is an important molecule and involved in various research fields, this developed composite reagent could be employed for many applications in biological analysis. As a proof-of-application demonstration, the sensitive detection of glucose was conducted. Moreover, the method was also extended to the detection of other biomolecules, such as cholesterol and horseradish peroxidase, which indicated the broad applications of the proposed sensing strategy in biomedical analysis.
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Advanced Optical Materials
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2025
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IF 7.2
Lin Shi,Junchun Li,Zengce Liu,Ping Chen,Yang Jiang
Rare-earth metal halides have emerged as a compelling class of luminescent materials, offering an environmentally benign alternative to toxic lead-based halides. This work reports the successful synthesis of Cs 3 CeX 6 (X = Cl, Br, I) with tunable emission and excellent photoluminescence quantum yield (PLQY) of Cs 3 CeCl 6 . Through controlled halogen substitution in the Cs 3 CeX 6 (X = Cl, Br, I) system, composition-dependent emission redshift (Cl→Br→I) is observed. Among them, Cs 3 CeCl 6 achieves a photoluminescence quantum yield (PLQY) of 99.89%, significantly surpassing the 92.57% PLQY of Cs 3 CeBr 6 and the 7.53% PLQY of Cs 3 CeI 6 , meanwhile surpassing that of most previously reported lead-free metal halides, highlighting its exceptional potential for efficient luminescent applications. Thermal stability analysis reveals that Cs 3 CeCl 6 maintains remarkable emission efficiency at elevated temperatures, retaining > 85% of its room-temperature luminescence intensity at 438 K, compared to only 60% for Cs 3 CeBr 6 and a mere 10% for Cs 3 CeI 6 . The exceptional thermal robustness originates from their characteristically high activation energies for thermal quenching, which effectively suppress non-radiative relaxation pathways. White light-emitting diodes (LEDs) based on Cs 3 CeI 6 exhibit a remarkable color rendering index (R a ) of 95.1, in contrast to those based on Cs 3 CeCl 6 (R a = 77.6) and Cs 3 CeBr 6 (R a = 79.6); all WLEDs based on Cs 3 CeX 6 (X = Cl, Br, I) demonstrate excellent atmospheric stability. With near-unity PLQY and remarkable thermal stability of Cs 3 CeCl 6 , coupled with the outstanding white LEDs performance of Cs 3 CeI 6 , Cs 3 CeX 6 (X = Cl, Br, I) compounds emerge as promising candidates for next-generation environmentally friendly optoelectronic applications, particularly in advanced display technologies and solid-state lighting systems. This work contributes to the advancement of eco-friendly emitters with both high efficiency and practical utility in next-generation optical technologies.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2025
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IF 8.5
Bangfeng Fu,Ruilei Yang,Liang Zhang,Weijie Gong,Ximei Han,Bingzhi Li,Qianjin Liu,Jianlong Wang
With the escalating focus on sustainable food packaging, the concurrent demands for outstanding mechanical robustness and effective photodynamic antibacterial activity in materials designed for fruit preservation have yet to be adequately fulfilled. This study first engineered an innovative food packaging nanocomposite (CPBI) through strategic integration of BiOBr/I heterojunction within a polyvinyl alcohol/carboxymethyl cellulose (PVA/CMC) matrix, integrating photodynamic antibacterial functionality and ultra-high mechanical strength for perishable fruit preservation. The incorporation of BiOBr/I into the natural-polymer network achieved remarkable pathogen inactivation efficiencies of 97.4 % against Staphylococcus aureus and 93.8 % against Escherichia coli O157:H7 via ROS-mediated membrane peroxidation. Simultaneously, the CPBI film displayed superior mechanical properties (tensile strength: 240.1 MPa, fracture strain: 260 %). In practical storage, this film successfully extended the shelf life of cherry tomatoes to 20 days, demonstrating its highly effective fruit preservation capability. This strategy advances the evolution of intelligent packaging solutions, simultaneously addressing the tripartite challenges of material sustainability, postharvest preservation, and foodborne pathogen mitigation.
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JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
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2014
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IF 3.679
Sheng-Jie Chen,Yong-Qi Li,Yong-Yong Wang,Xiao-Li Zhao,Ye Liu
The ionic hybrid P,N-ligands of 1 and 2 have been synthesized as one type of unconventional tertiary phosphines with the advantages of both the π-accepting ligands and the hemilabile ligands. The corresponding ionic Rh(I)-complexes of 1A and 2A proved to be more efficient catalysts for hydroformylation of 1-octene over isomerization than the traditional Rh I (acac)(CO)(PPh 3 ), due to the π-backdonation interaction in Rh → P linkage and the hemilabile ligation of N,P-coordinating sites to Rh-center. The in situ high-pressure FT-IR analysis indicated that: (1) the formation and lifetime of the active Rh H species (2047 cm −1 ) derived from 1A are facilitated by the presence of ligand 1 ; (2) the formation of the active Rh H species is depressed without the aid of the P,N-hemilabile ligation; and (3) the active Rh H species derived from Rh I (acac)(CO)(PPh 3 ) is unstable and susceptible to the formation of the inactive carbonyl-bridged Rh-dimer.
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JOURNAL OF ORGANIC CHEMISTRY
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2020
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IF 4.335
Lujia Mao,Chunlei Li,Libo Xiang,Dejun Fu,Wangyang Ma,Qing Ye
The synthesis of allenyl-Bdan has been realized via the Cu(I)-catalyzed borylation of propargylic alcohols. This methodology offers a facile and efficient pathway toward allenyboronates with diverse functional groups due to the simple access to the substrates. The substrates bearing ester groups are well-tolerated in the synthesis of allenyl-Bdan under the Lewis acidic conditions. The structures of two allenyl-Bdan were further confirmed via single-crystal X-ray diffraction.
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