BIOMACROMOLECULES
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2024
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IF 5.5
Danyu Lv,Wanjun He,Wei Liu,Yuqiang Cheng,Yan Cui,Xiujuan Zhou,Yanwen Xue,Siming Yu,Ningjin Zhang,Hecheng Meng,Yongguang Guan,Jian-He Sun,Xian-Ming Shi
The γ-cyclodextrin (γ-CD) metal–organic frameworks (CD-MOF-1) consist of γ-CD and potassium (K+) ions through coordinating an eight-coordinated K+ ion with two C5-linked oxygen and C6-linked hydroxyl (C5–O/C6–OH) groups in the primary faces of adjacent γ-CD units and two C2- and C3-linked hydroxyl (C2–OH/C3–OH) groups in the secondary faces. Herein, we found polysaccharide gels with only C2–OH/C3–OH or C5–O/C6–OH groups in pyranoid rings can form four-coordinated K+ ions and then coordinate γ-CD in a KOH solution for CD-MOF-1 growth. Exposure of C2–OH/C3–OH or C5–O/C6–OH groups in polysaccharide gels is important to form active four-coordinated K+ ions. Mechanism supporting this work is that four-coordinated K+ ion sites are first formed after coordinating C2–OH/C3–OH groups in pectin and then coordinating C5–O/C6–OH groups in the primary faces of γ-CD units. Alternatively, four-coordinated K+ ions with C5–O/C6–OH groups in chitosan can coordinate the C2–OH/C3–OH groups in the secondary faces of γ-CD units. Mechanism of CD-MOF-1 growing on pectin and chitosan gels through the proposed four-coordinated K+ ions is also universally applicable to other polysaccharide gels with similar C2–OH/C3–OH or C5–O/C6–OH groups such as alginate gel. Based on this mechanism, we developed pectin and chitosan gel-based CD-MOF-1 composites and exemplified applications of them in antibacterial and organic dye removal. To help future research and applications of this mechanism, we share our theoretical assumption for further investigations that any matrices with an ortho-hydroxyl carbon chain or ortho-hydroxyl ether structures may form four-coordinated K+ ions for CD-MOF-1 growth. The proposed mechanism will broaden the development of novel CD-MOF-1 composites in various fields.
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高影响因子
MICROCHEMICAL JOURNAL
·
2026
·
IF 5.2
Guoliang Zhang,Yaolong Zhang,Yu Zhang,Changshun Wang,Jin Tan,Ruxangul Jamal,Tursun Abdiryim,Ahmat Ali
Hydroxyl-functionalized MWCNs and PEDOT are better suited for loading MIP. • The sensor detects pefloxacin at the picomolar level. • Synthesis of ultra-thin tubular PEDOT-OH@Au/MWCNs-OH nanocomposites. • The excellent thin-layered structure offers an efficient electron transport pathway. To safeguard public health and prevent the increase of bacterial resistance, the creation of practical and accurate detection methods for the quantitative analysis of fluoroquinolone antibiotics is essential. In this study, a tubular PEDOT-OH@Au/MWCNTs-OH substrate material was prepared using a one-step in situ oxidation method, with chloroauric acid as the oxidant. Pyrrole (Py) was used as the functional monomer, and pefloxacin (PFX) as the template molecule, to ingeniously design a molecularly imprinted electrochemical sensor (MIP/PEDOT-OH@Au/MWCNT-OH) with sensitive sensing capabilities. As expected, the unique structure and properties of PEDOT-OH@Au/MWCNTs-OH provided the sensor more surface area and enhanced electrochemical activity, increasing the number of distinct recognition sites. Based on experimental results, the MIP/PEDOT-OH@Au/MWCNT-OH sensor showed good anti-interference and stability, a low detection limit of 0.149 nM, S/N = 3, and a broad linear range of 0.002–30 μM. Additionally, the sensor achieved a recovery rate of 97%–103% in detecting PFX in pefloxacin mesylate ointment. This sensor shows promise as a highly selective and sensitive portable detection method for the quantitative analysis of PFX in the environmental monitoring. Download: Download high-res image (239KB) Download: Download full-size image
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2018
·Vol. 102
·期 3
·1414-1424
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IF 2.956
Yaowu Wei,Tao Zhang,Qi Zhang,Bingqiang Han,Nan Li
Improving the hydration resistance of CaO aggregates is the key to successful application of lime-based refractories in metallurgical industry. Additive Zr(OH) 4 and Al(OH) 3 were introduced in the preparation of CaO granules using granulation equipment and calcination method in this study. The results showed that the hydration resistance of CaO granules was improved significantly, especially for granules with 0.6 wt.% Zr(OH) 4 and 0.9 wt.% Al(OH) 3 , respectively. The shell of CaO granules was relatively dense after calcination and the volume of open pores of CaO granules decreased from 3.56 × 10 −2 to 1.80 × 10 −2 cm 3 /g when additive was introduced. Zr(OH) 4 and Al(OH) 3 have the opposite effect on the closed porosity of CaO granules, the closed porosity of CaO granules was decreased with Zr(OH) 4 addition, but increased with Al(OH) 3 addition.
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INORGANIC CHEMISTRY
·
2024
·
IF 4.3
Ya-Lan Deng,Chun-Li Hu,Jiang-Gao Mao
The π-conjugated [C3H6+xN6]x+ (x = 0–3) cations are good functional groups, which are widely employed in the preparations of nonlinear optical (NLO) and birefringent materials due to their high hyperpolarizability and optical anisotropy. In this paper, the first melamine hydroxyborate [C3H7N6]3[B3O5(OH)2] (MelBO-I) was synthesized by the boric acid melting method under the molar ratio of H3BO3:C3H6N6 = 1:1. MelBO-I (P21/c) exhibits a two-dimensional (2D) {[C3H7N6]3[B3O5(OH)2]}∞ layer composed of [C3H7N6]+ cations and [B3O5(OH)2]3– anions interconnected via hydrogen bonds. MelBO-I exhibits significant birefringence (Δn = 0.286@546 nm). Under the molar ratio of H3BO3/C3H6N6 = 3:1, [C3H8N6]4[B12O19(OH)6] (MelBO-II) was isolated. In MelBO-II (P21), highly polymerized [B12O19(OH)6]8– groups form a 3D network through hydrogen bonding, featuring 1D tunnels of 8-membered and 16-membered rings filled by [C3H8N6]2+ cations. MelBO-II is the first noncentrosymmetric (NCS) bifunctional melamine borate with a moderate SHG response (0.4 × KDP) and large birefringence (Δn = 0.285@546 nm). The results indicate that incorporating [C3H6+xN6]x+ (x = 0–3) cations into borate can effectively induce birefringence. A high concentration of boric acid promotes the formation of large boric acid cluster anions and facilitates the transformation from the CS to NCS structure.
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ANALYTICAL LETTERS
·
2025
·
IF 1.8
Hongdan Wang,Xixi Song,Qianqian Wu,Tingting Yu,Ting Lin,Yiran Yu,Zhenxiao Dai,Hongyan Bai
Zeolitic imidazolate framework-67 (ZIF-67) was firstly synthesized using cobalt (II) chloride hexahydrate and 2-methylimidazole. Then, glucose molecules were adsorbed into the ZIF-67 microporous structure and ZIF-67 loaded with carbon quantum dots (CQDs-ZIF-67) were synthesized by low-temperature calcination. CQDs-ZIF-67 and nickel chloride hexahydrate (II) were dissolved in anhydrous ethanol and CQDs/Co2(OH)3Cl/NiCl(OH) nanocomposites were synthesized by a hydrothermal method. A nonenzymatic glucose electrochemical sensor based on a glassy carbon electrode (GCE) modified by CQDs/Co2(OH)3Cl/NiCl(OH) was constructed and exhibited a wider linear range and a lower detection limit for glucose detection due to the abundant pore structure and good electrocatalytic activity of CQDs/Co2(OH)3Cl/NiCl(OH).
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IONICS
·
2022
·Vol. 28
·期 8
·3945-3956
·
IF 2.961
Wei Xuedong,Chai Yudan,Chen Weifeng,Liu Nan,Qiao Shuangyan
In this paper, an amorphous composite electrocatalyst of Co(OH) 2 -Ni(OH) x S y was prepared by a simple and rapid electrochemical deposition method on nickel foam (NF). The electrochemical performance for oxygen evolution reaction (OER) was tested in 1 M KOH solution. The overpotential of Co(OH) 2 -Ni(OH) x S y (Co:Ni = 9:1) electrode was 423 mV at 50 mA cm −2 . The potential of the Co(OH) 2 -Ni(OH) x S y (Co:Ni = 9:1) sample remained essentially unchanged from the initial potential of 1.651 V after 12 h of stability test. In this catalyst, the strong synergistic effect between cobalt and nickel ions, the greatly increased amorphous defect sites and oxygen vacancies, and the abundant electrochemical specific surface area together lead to the increased electrocatalytic activity and high electrocatalyst stability. This amorphous CoNi-based composite electrocatalyst prepared by simple electrodeposition has certain significance for the preparation of hydrogen energy.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Kaitong Liu,Jian Han,Fuming Li,Congcong Jin,Zhihua Yang,Miriding Mutailipu,Shilie Pan
A case of hydrous borate with the formula of Ba 2 B 13 O 19 (OH) 5 ·5H 2 O was synthesized by the traditional hydrothermal method . It crystallizes in the chiral P 1 space group and has a unique two-dimensional 2 [B 13 O 19 (OH) 5 ] ∞ layer that is constructed by the hydrogen involved [B 13 O 22 (OH) 5 ] fundamental building blocks (FBBs). The Ba atoms and H 2 O molecules are filled in the three-dimensional pore constructed by the 2 [B 13 O 19 (OH) 5 ] ∞ layer. Interestingly, Ba 2 B 13 O 19 (OH) 5 ·5H 2 O is the first case of hydrous borates that has the above rare [B 13 O 22 (OH) 5 ] FBB and 2 [B 13 O 19 (OH) 5 ] ∞ layer, which enriching the structural chemistry of borate system. The diffuse reflection spectrum result shows that the ultraviolet (UV) cutoff edge of Ba 2 B 13 O 19 (OH) 5 ·5H 2 O is below 200 nm. Its second harmonic generation (SHG) response is approximately 1.0 times that of potassium dihydrogen phosphate at the 1064 nm fundamental wavelength and it is also phase-matchable. Both results indicate that the title compound is a nonlinear optical crystal for UV spectral region. Theoretical simulation calculation shows that the occupied VE states are mainly contributed by the O-2p orbitals, and therefore [B 13 O 22 (OH) 5 ] groups are the main sources of SHG effects.
研究领域:
无机化学
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材料科学
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晶体工程
·
光学材料
·
固体化学
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Chemistry-An Asian Journal
·
2024
·
IF 3.5
Xinxin Dai,Zhen Tang,Xinyuan Yan,Shiyi Tao,Shanshan Wang,Yi Liu,Jiafeng Cao,Xiaolong Deng,Xin Bo
The exploring and developing non-precious transition metal-based catalysts for practical water electrolysis with the low cost, high efficiency and easy macroscopic preparation was still a challenge. Herein, Ni 3 S 2 /Ni(OH) 2 heterojunction with different sulfuration time was proposed and hydrothermally synthesized using a simple two-step approach, which served as a bifunctional electrocatalyst for water splitting in alkaline solution at industrial temperature. Among these catalysts, Ni 3 S 2 /Ni(OH) 2 -5h displayed the smallest overpotentials (237 mV@100 mA cm −2 and 360 mV@100 mA cm −2 ) for OER and HER at room temperature, along with low Tafel slopes of 62.0 mV dec −1 and 80.8 mV dec −1 respectively. Furthermore, working at high temperature Ni 3 S 2 /Ni(OH) 2 -5h exhibited even lower overpotential of 82 mV@100 mA cm −2 at 70 °C for OER and 325 mV@100 mA cm −2 at 60 °C for HER. The excellent performance was ascribed to the heterojunction accelerating the charge transfer, hierarchical interconnected structure promoting the mass transfer and the synergistic effect between the components of Ni 3 S 2 and Ni(OH) 2 . This work could provide a promising route for promoting the electrocatalytic performance of Ni-based catalyst with a simple sulfuration method for industrial water splitting, which could expand to other non-noble metal-based materials for enhancing the electrocatalytic activities.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Qian Wang,Chensheng Lin,Guohong Zou,Mengjiao Liu,Daojiang Gao,Jian Bi,Ling Huang
A new noncentrosymmetric material, namely, K 2 [B 3 O 3 (OH) 5 ] has been obtained by conventional solution reaction. It crystallizes in the orthorhombic space group Ama 2 (no. 40). In the structure of K 2 [B 3 O 3 (OH) 5 ], the BO 2 (OH) triangles and BO 2 (OH) 2 tetrahedra are linked via sharing corners forming the isolated [B 3 O 3 (OH) 5 ] 2- anionic groups with no dangling bonds in oxygen atoms. And K 2 [B 3 O 3 (OH) 5 ] is the first synthetic noncentrosymmetric borates with [B 3 O 3 (OH) 5 ] 2- anionic groups. Powder second-harmonic generation (SHG) using the Kurtz−Perry technique showed that K 2 [B 3 O 3 (OH) 5 ] is type I phase-matchable, and the measured SHG coefficient is 0.32 times that of KH 2 PO 4 . The UV transmittance spectroscopy measurement indicated that the UV absorption edge was below 200 nm, suggesting that K 2 [B 3 O 3 (OH) 5 ] might be a promising deep-UV nonlinear optical material. Band structure and optical property calculations based on DFT methods were also performed.
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INORGANIC CHEMISTRY
·
2022
·
IF 5.436
Ru-Ling Tang,Mei Yan,Wen-Dong Yao,Wenlong Liu,Sheng-Ping Guo
Oxyhalides possessing the merits of oxides and halides have widely received attention for their comprehensive physical performances, especially as potential nonlinear optical (NLO) crystals. Here, based on conventional strategy for obtaining acentric compounds, a Te4+ lone-pair cation was introduced into oxyhalides, and one oxyfluoride, HgTeO2F(OH), was obtained via a hydrothermal reaction. Crystallized in the polar space group Pca21, the layered structure of HgTeO2F(OH) is composed of V-shaped [HgO2]2– groups and [TeO2F(OH)]2– pyramids, in which the [TeO2F(OH)]2– pyramid first served as the NLO functional motif. Its powder sample exhibits a phase-matchable SHG response of 1.1 × KH2PO4 at 1064 nm, and its birefringence (0.09@1064 nm) is sufficient for phase-matchable behavior, which manifests its comprehensive capacity as a promising NLO candidate. Theoretical calculations about electronic structure and optical properties are also carried out, revealing that the Te4+ lone-pair cation makes the predominant contribution to the SHG effect and synergizes with the [HgO2]2– groups.
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POLYMER TESTING
·
2022
·
IF 4.931
Yuezhou Liu,Yanjing Liu,Xiyue Li,Yongfang Qian,Lihua Lv,Ying Wang
In order to fabricate antibacterial nanofiber membranes for tissue engineering field, the oxidative damage of magnesium hydroxide nanoparticles (Mg(OH) 2 NPs) against the model system of Escherichia coli ( E. coli ) was researched by measuring the oxidative stress response, oxidative stress products and glucose metabolism. The toxicity of Mg(OH) 2 NPs to a normal biological system was evaluated in vivo through the acute oral toxicity, blood physiological and serum biochemical markers and acute skin irritation, indicating that the Mg(OH) 2 NPs exhibited great biosafety. The Mg(OH) 2 NPs with antibacterial property and biosafety were loaded on PCL/PVP nanofiber substrates through electrospinning technology to fabricate the Mg(OH) 2 /PCL/PVP nanofiber membranes. The results of characterization and antibacterial test showed that the Mg(OH) 2 /PCL/PVP nanofiber membranes with 8.0 wt% Mg(OH) 2 NPs present excellent antibacterial rate of 100% against E. coli that the Mg(OH) 2 NPs can be physically and evenly loaded on nanofiber substrates.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2020
·
IF 3.807
Fuling Zhou,Chao You,Qiang Wang,Yilin Chen,Zhipeng Wang,Zuoping Zeng,Xuping Sun,Ke Huang,Xiaoli Xiong
A novel highly sensitive non-enzymatic glucose sensor is constructed based on an ultrafast synthesized amorphous NiCu-OH film coated Cu(OH) 2 nanorod array grown on copper foam (NiCu-OH@Cu(OH) 2 NRA/CF). The synthesized (NiCu-OH@Cu(OH) 2 NRA/CF) has abundant catalytic activity and good catalytic performance for the electrochemical detection of glucose in alkaline conditions. Sensitive and selective voltammetric detection of glucose is demonstrated. The linear range extends from 100 nM to 1.5 mM, the detection limit is 32 nM, and the sensitivity is 6560.3 μA mM -1 cm -2 . The method is applied to the determination of nitrite in human blood serum.
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