INORGANICA CHIMICA ACTA
·
2021
·
IF 2.545
Dan Zheng,Ting-Hong Huang,Cheng Luo,Jing Tang
Three dinuclear Cu(I) complexes, [Cu 2 (pnd)(PPh 3 ) 4 ](BF 4 ) 2 (1) , [Cu 2 (pnd)(dppp) 2 ] (BF 4 ) 2 (2) , and [Cu 2 (pnd)(DPEphos) 2 ](BF 4 ) 2 (3) (PPh 3 = triphenylphosphine , dppp = 1, 3-bis (diphenylphosphino)propane, DPEphos = bis(2-diphenylphosphinophenyl)ether, pnd = N , N ’-bis (pyridin-2-ylmethylene)naphthyl-1, 5-diimine), have been prepared and characterized by IR, 1 H NMR, 31 P NMR, 13 C NMR, XRD , elemental analysis and X-ray crystal structure analysis. The structural analysis reveals that the flexible pnd in 1 – 3 acts in a trans bridging coordination mode to connect two Cu + ions, forming a S-shape conformation, while each of Cu (I) ion is four-coordinate N2P2, adopting a distorted-tetrahedral geometry. DFT calculations show that the HOMOs of complexes 1 – 3 are primarily located on the copper d -orbital and the phosphine ligand, together with a specific contribution of pnd, while LUMOs are mostly composed of pnd with admixed Cu(I) d-orbital character. Corresponding calculations of atomic charges indicate that the charge of the copper atom in complexes 1 – 3 is below + 1, while the total charges of the coordinated atoms are 0.743–0.786. Moreover, the solid-state emission spectra of complexes 1 – 3 show the existence of broad emission bands at 350–550 nm.
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JOURNAL OF STRUCTURAL CHEMISTRY
·
2018
·Vol. 59
·期 3
·744-747
·
IF 0.521
Sun S.-W.,Wang G.-F.
The synthesis of a novel Cu(I) complex with V-shaped bidentate ligands {[Cu(BIPMO)]×[CuBr 2 ]} n where BIPMO = bis(4-(1 H -imidazol-1-yl)phenyl)methanone is reported. It is characterized by IR spectroscopy, elemental analysis, and single crystal X-ray diffraction. Copper(I) ions in the complex are in a distorted environment in which donor atoms are provided by the bromide anion and nitrogen atoms of BIPMO ligands, respectively. Infinite anion chains formed by CuX 4 (X = Br or N) polyhedra are linked by BIPMO ligands to give rise to layers. Furthermore, the layers are linked into 3D networks through weak intermolecular interactions.
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FOOD CONTROL
·
2022
·
IF 6.652
Xuanyu Sha,Siqingaowa Han,Guoqiang Fang,Nan Li,Dianyang Lin,Wuliji Hasi
In this work, a facile and effective method for assembly and transfer nanoparticles on thin layer chromatography (TLC) plate was proposed and used to combined with layer chromatography-surface-enhanced Raman spectroscopy (TLC-SERS) strategy for detection of Rhodamine B and Sudan I. First, Monodispersed Ag NCs with broadly tunable diameters (from 41 to 67 nm) and 7.25 × 10 5 maximum actual enhancement factor (AEF) were successfully prepared and systematically investigated for its optic performance use in TLC-SERS. Au@Ag NCs were monitored by TEM, SEM and UV–Vis spectrometer. The optical properties of Ag NCs were simulated and the experimental results showed good consistency with simulation results of absorption spectra. Through three phases interfacial technique and a simple transfer method, nanostructures were assembled on the TLC plate. Moreover, the semi-quantitative analysis of Rhodamine B and Sudan I in the range of 1–200 ppm was performed based on the assembled TLC plate with the limit of detection as low as 1 ppm. In addition, the practical feasibility of this strategy was verified by the detection of Sudan I and Rhodamine B in chili oil. In general, this assembled TLC-SERS strategy builds a connection for the application of nanomaterials with rich morphology in TLC-SERS, which has a great application prospect and practical application value.
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Journal of Physical Chemistry C
·
2013
·
IF 4.814
Lei Huang,Xiuli Wang,Jinhui Yang,Gang Liu,Jingfeng Han,Can Li
The photocatalytic activity and stability of nanocrystals (NCs) are two important issues for their application in photocatalysis. In this work, we report a combined method to promote the photocatalytic activity as well as the stability of CdS NCs for photocatalytic H2 evolution. ZnS shell was grown on CdS NCs forming type I core/shell CdS/ZnS nanocrystals (NCs) to restrain the photocorrosion and passivate the trap states on CdS NCs. Thereafter, dual cocatalysts were loaded to promote the separation and transfer of electrons and holes from the core to outer surface for photocatalytic reactions. It is found that Pt and Ni are effective reduction cocatalysts (RCs) while PdS and PbS are effective oxidation cocatalysts (OCs) for promoting the charge separation and transfer. This strategy was also proved to be effective for other type I core/shell NCs, such as CdTe/CdS/ZnS NCs.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2025
·
IF 4.6
Kai Wang,Yan-Ru Wang,Jun Zhao,Ren-Min Zhou,Xi-Feng Xu,Tong Wang,Zhong-Yuan Cheng
Hepatic ischemia-reperfusion (I/R) injury is a major clinical complication, and the precise monitoring of key inflammatory mediators like neutrophil elastase (NE) in vivo remains a significant challenge. To address this, we developed HDS-NE, a highly specific and activatable molecular probe based on a sulfur-substituted hemicyanine scaffold, engineered for the simultaneous detection of NE via fluorescence and photoacoustic imaging modalities. The probe demonstrated exceptional sensitivity and selectivity toward NE, enabling the real-time visualization of elevated NE activity in a murine model of hepatic I/R injury. Both in vivo and ex vivo imaging results confirmed a markedly enhanced signal in injured livers compared to controls, which was further validated by serum assays and histology. Crucially, this study represents the successful achievement of non-invasive, in vivo imaging of NE activity during hepatic I/R processes, offering a powerful tool for diagnosing and studying inflammatory liver diseases.
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PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Yifan Liu,Yiyu Yang,Minjie Peng,Wen Zang,Chaozhen Wang,Yuenan Zhang,Changyong Gao,Aiguo Wu,Yujie Zhang
Heparin, as a glycosaminoglycan with multiple physiological functions, performs important roles in clinical practice. The core function of heparin is its anticoagulant effect, which is commonly used to prevent and treat thrombotic diseases. However, when the heparin content in human blood exceeds the standard, it can result in thrombocytopenia, thereby posing threat to human health. Therefore, rapid, sensitive and accurate detection of heparin is of great practical importance in assessing the anticoagulant effect, prevention of thrombophilia, guidance on personalized medication, and avoiding side effects caused by excessive use. A new colorimetric sensor for detecting the anticoagulant heparin is introduced in this work. The sensor is low cost, fast, and simple. In the absence of heparin, protamine protects copper‑gold nanoparticles from the etching of iodide ions through electrostatic interaction, and the solution's color and spectral properties remain essentially the same as those of pure copper‑gold nanoparticles. When heparin is present, due to the strong electrostatic adsorption between heparin and protamine, protamine preferentially binds heparin and forms a complex. Cu-Au NPs are not protected and are etched into spherical Au NPs by iodide ions. The solution's color shifted from dark gray and purple to pink, thus colorimetric detection of heparin is realized rapidly based on the etching mechanism. The detection time is 15 min, and the detection limit is as low as 1 ng/mL. Compared with HPLC detection method, the colorimetric detection of heparin in serum samples has the recovery rate of 98.8–108.8 %, which has good prospects for application.
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产品关联
DOI
高影响因子
BIOMATERIALS
·
2025
·
IF 12.9
Yuchao Sun,Jian He,Weiyu Chen,Yongfang Wang,Kai Wang,Min Zhou,Yichun Zheng
High-dose radiation therapy is a widely used clinical strategy to inhibit tumor growth. However, the rapid generation of excessive reactive oxygen species (ROS) triggers the formation of neutrophil extracellular traps (NETs), which capture free tumor cells in the bloodstream, promoting metastasis. In this study, we developed a hybrid nanoparticle composed of DNase I and gold (DNase I@Au) to enhance radiotherapy efficacy while mitigating metastasis by precisely eliminating NETs. The DNase I@Au nanoparticles, administered via aerosol inhalation, are efficiently delivered to lung tumor tissue, improving radiosensitization and reducing tumor size. Crucially, the nanoparticles could gradually release DNase I, effectively degrading ROS-induced NETs and preventing the interaction of free malignant cells with tumor sites or vasculature, thereby inhibiting metastasis. Therefore, we provide an enzyme and sensitizer co-loaded strategy that offers a promising approach to improve the therapeutic outcome of radiotherapy and reduce the risk of lung cancer metastasis under ROS stimulation.
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DOI
PubMed
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2017
·
IF 2.843
Ya-Wen Zhang,Guan Wu,Hui Dang,Kangzhe Ma,Su Chen
Organometal halide perovskites (such as CH3NH3PbX3, X = Cl, Br, I) have received enormous interest due to their strikingly photoelectric properties. Here we develop a facile ligand-assisted reprecipitation method to synthesize NH2CH═NH2PbX3 (NH2CH═NH2+, FA; X = Br and I) perovskite quantum dots (QDs) at room temperature. The FAPbX3 perovskite QDs with uniform monodispersity (sized 4–7 nm) display relatively high photoluminescence quantum yields (PLQYs) of 60–75%. Through manipulating the mixed-organic-cation reactions, we achieve a series of multicolored perovskite QDs with continuously controllable emission wavelengths from 460 to 565 nm. Furthermore, we discuss the influence of ligands (oleic acid and n-octylamine) on PL properties and stabilities of perovskite QDs. Finally, we have successfully designed a white LED via compositing perovskite QDs and poly(methyl methacrylate) (PMMA), which presents a high color rendering index. Considering those remarkable achievements, we believe our work will have great potential to meet various optoelectronic applications.
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Journal of Cleaner Production
·
2021
·
IF 9.297
Chuankun Yin,Siji Zhou,Keyi Zhang,Jiale Bai,Yangyang Lv,Xuewen Zhang,Xiaoxia Li,Aihua Xu
p-Nitrophenol (PNP) is one of the highly toxic and mutagenic pollutants existed in aquatic environment. In this work, the crednerite CuMnO 2 nanoflake was prepared and used to degrade PNP with peroxymonosulfate (PMS) as the oxidant. It was found that CuMnO 2 exhibited much higher activity than other Cu-based catalysts such as CuO, Cu 2 O, CuFe 2 O 4 and CuFeO 2 , with 90% of PNP degraded after 10 min under mild reaction conditions. The catalyst was also stable during five successive runs. Sulfate and hydroxyl radicals produced from PMS reduction by Cu(I) species, as well as superoxide ions and single oxygen, contribute to the degradation of PNP. More importantly, the interactions between Mn and Cu species in CuMnO 2 were identified by X-ray photoelectron spectroscopy (XPS), fourier transform infrared spectroscopy (FT-IR) and linear sweep voltammetry (LSV), and were further confirmed by the control experiment with the mixture of Cu 2 O + Mn 2 O 3 . The results implied that the high valent Mn(III) species acted as Lewis acids to withdraw electron from PMS, resulting that the Cu(I) species can be easier oxidized to Cu(II) by PMS with the formation of radicals. These findings provide an ideal bimetallic heterogeneous catalyst and a new mechanism for PMS-mediated reaction.
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JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2022
·
IF 3.119
Li Chen,Lingbin Shen,Yuhang Chen,Zhengyang Luo,Zexin Ren,Rongrong Li,Cunbin Du
The solubility data of nimesulide (form I) in different mono- and mixed solvents over the temperature range from 273.15 to 318.15 K are determined. In this work, it is further studied to improve the solubility data of nimesulide (form I) and analyze the intermolecular force. The solubility profiles in mono- and mixed solvents are correlated by some thermodynamic models. The results of statistical analysis show that all selected models could provide a good correlation of the dissolution profile for nimesulide in selected solvents at all investigated temperatures. At 318.15 K, the largest solubility in mole fraction is obtained in acetone (7.812 × 10–2), followed by 2-butanone (6.334 × 10–2), cyclohexanone (4.977 × 10–2), ethyl acetate (3.803 × 10–2), tetrahydrofuran (3.651 × 10–2), acetonitrile (2.975 × 10–2), ethanol (2.169 × 10–3), toluene (1.788 × 10–3), isobutanol (1.348 × 10–3), isopropanol (1.201 × 10–3), and propylene glycol (PG, 6.764 × 10–4). However, in mixtures of (ethyl acetate + isopropanol), the solubility data increase with the increase of the mass fraction of ethyl acetate at a given temperature. The effect of solute–solvent interactions on the solid–liquid phase equilibrium of the solute is discussed with the solvent properties. The calculation of preferential solvation parameters shows that solute molecules are preferentially solvated by isopropanol in isopropanol-rich regions and as the mass fraction of ethyl acetate increases, nimesulide is preferentially solvated by ethyl acetate. Studying the dissolution process of nimesulide is of great practical significance for its purification.
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LETTERS IN ORGANIC CHEMISTRY
·
2024
·Vol. 22
·期 1
·56-60
·
IF 0.7
Xin-Yu Lin,Guo-Jun Chen,Su-Zhe Wu,Ke-Xuan Xu,Xiao-Tian Zhang,Qi Feng
4-Hydroxyquinoline-2(1H)-ones exhibit multiple biological activities, and studying their synthetic methods is of great significance. In the presence of tetramethylguanidine and silver nitrate, 4-hydroxyquinoline-2(1H)-ones were efficiently synthesized from 2-ethynylanilines and carbon dioxide under atmospheric pressure. The reaction conditions, such as types of silver catalysts and reaction solvents, were optimized, and the applicability of the substrate was preliminarily investigated. This method provides an alternative pathway for the synthesis of 4-hydroxyquinoline-2(1H)-ones and the conversion and utilization of carbon dioxide.
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Desalination and Water Treatment
·
2024
·
IF 1
Song Deng,Jingrong Huang,Meng Guo,Xueni Sun,Xiuxiu Ren,Jing Zhong,Rong Xu
Novel p-phenylenediamine-bridged organosilica (PPDA-BOS-T) materials were synthesized via the co-condensation reaction assisted by tetraethyl orthosilicate (TEOS). These amino-functionalized organosilicas were characterized by Fourier transform infrared spectrometer, N 2 sorption, scanning electron microscopy, and transmission electron microscopy. The addition of TEOS played a positive role in the construction of the porous network structure of the bridged organosilicas. The saturation adsorption capacity for Ag(I) of the PPDA-BOS-T could reach 82.88 mg g –1 . The conformity to the Freundlich model indicated multilayer adsorption with active sites. Furthermore, the adsorption was followed well by the pseudo-second-order model, and the intraparticle diffusion was proved to be the rate-limiting step during the adsorption of Ag(I). Finally, the thermodynamic parameters including the change of free energy (ΔG), enthalpy (ΔH), and entropy (ΔS) of adsorption were calculated.
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