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Chemistry of Heterocyclic Compounds · 2018 ·Vol. 54 ·期 2 ·125-129 · IF 1.201

A 3-hydroxyflavone derivative as fluorescence chemosensor for copper and zinc ions

Gao Huiqin,Wu Xiangwen

A 3-hydroxyflavone derivative as fluorescence chemosensor for copper and zinc ions has been synthesized. Its recognition properties for copper and zinc ions in aqueous solution were investigated based on UV-vis absorption and fluorescence spectra change. The compound exhibits color change from colorless to yellow and quenching of green fluorescence in the presence of copper ions in aqueous solution due to coordination reaction. In turn, the addition of zinc ions induces the color change from colorless to green and fluorescence enhancement of the compound. The complex ratios between the sensor molecule and copper(zinc) ions are 1:1 and 1:2, respectively, based on the Job's plots and in situ mass spectra. Thus, this compound can selectively recognize copper and zinc ions, and the recognition also can be observed by naked eye.

CAS / MDL: 582-24-1 7570-45-8
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ACS Applied Materials & Interfaces · 2018 · IF 8.097

Porous NaTi2(PO4)3/C Hierarchical Nanofibers for Ultrafast Electrochemical Energy Storage

Peng Wei,Yanxiang Liu,Zhihao Wang,Yangyang Huang,Yu Jin,Yi Liu,Shixiong Sun,Yuegang Qiu,Jian Peng,Yue Xu,Xueping Sun,Chun Fang,Jiantao Han,Yunhui Huang

NaTi2(PO4)3 (NTP) with a sodium superionic conductor three-dimensional (3D) framework is a promising anode material for sodium-ion batteries (SIBs) because of its suitable potential and stable structure. Although its 3D structure enables high Na-ion diffusivity, low electronic conductivity severely limits NTP’s practical application in SIBs. Herein, we report porous NTP/C nanofibers (NTP/C-NFs) obtained via an electrospinning method. The NTP/C-NFs exhibit a high reversible capacity (120 mA h g–1 at 0.2 C) and a long cycling stability (a capacity retention of ∼93% after 700 cycles at 2 C). Furthermore, sodium-ion full cells and hybrid sodium-ion capacitors have also been successfully assembled, both of which exhibit high-rate capabilities and remarkable cycling stabilities because of the high electronic/ionic conductivity and impressive structural stability of NTP/C-NFs. The results show that the nanoscale-tailored NTP/C-NFs could deliver new insights into the design of high-performing and highly stable anode materials for room-temperature SIBs.

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Chemistry-An Asian Journal · 2018 ·Vol. 13 ·期 21 ·3246-3253 · IF 3.692

Optimizing the Thermoelectric Performance of Poly(3-hexylthiophene) through Molecular-Weight Engineering

Sanyin Qu,Qin Yao,Bingxue Yu,Kaiyang Zeng,Wei Shi,Yanling Chen,Lidong Chen

Graphical Weight problem : Poly(3-hexylthiophene) (P3HT) films with various molecular weights are successfully prepared, and both their molecular structures and thermoelectric (TE) properties are investigated. The molecular weight of P3HT is found to have an important effect on the carrier-transport properties by affecting the molecular structure and, as a result, also has an effect on the TE performance. Poly(3-hexylthiophene) (P3HT) films with various molecular weights (MWs) were successfully prepared, and both their molecular structures and thermoelectric (TE) properties were investigated. It was found that the molecular weight of P3HT had an important effect on the carrier-transport properties by affecting the molecular structure and, as a result, also had an effect on the TE performance. The electrical conductivity of the P3HT films first increased upon increasing the molecular weight and then decreased at high molecular weights, whereas the Seebeck coefficient remained at the same level. As a result, the P3HT-M 50k (MW≈50 000 g mol −1 ) film reached an electrical conductivity of (103.8±1.2) S cm, which is more than 20 times higher than the electrical conductivity of P3HT-M 10k (MW≈10 000 g mol −1 ) and almost 30 % higher than the electrical conductivity of P3HT-M 100k (MW≈100 000 g mol −1 ). Consequently, the maximum TE power factor of P3HT-M 50k at room temperature was as high as (22.6±0.6) μW mK −2 , which is much higher than that of either P3HT-M 10k or P3HT-M 100k . Microstructure analysis combined with C-AFM suggested that carrier transport between most of the ordered and amorphous regions was unconnected in films with low molecular weights, and this resulted in a high migration barrier and poor carrier mobility. Upon increasing the molecular weight, the long molecular chain provided enough connectivity for the charge to move through the ordered regions, which decreased the carrier barrier and increased carrier mobility. Therefore, both the conductivity and Seebeck coefficient were significantly improved. However, a too-high molecular weight could cause more folding of the polymer chain, which would deteriorate the electrical-transport properties. The experimental results not only reveal the intrinsic effect of molecular weight on the electric transporting properties of conducting polymers but also suggest that molecular-weight engineering is an effective way to design and screen high-performance polymer TE materials.

CAS / MDL: 82113-65-3
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JOURNAL OF MOLECULAR LIQUIDS · 2024 · IF 5.3

CO2-triggered (3-aminopropyl)triethoxysilane-functionalized M-MOF-74 stabilized Pickering emulsions

Xiaoyan Pei,Wangyue Song,Yunlei Shi,Yang Zhao,Zhiyong Li

Pickering emulsions with a stimulus response have been paid extensive concern due to their long-term stability and demulsification on-command. Metal-organic frameworks (MOFs) are expectable emulsifying agents to build Pickering emulsions based on their excellent properties such as high specific surface area, adjustable porosity and pore size. Herein, a novel kind of CO 2 -triggered Pickering emulsions formed by (3-aminopropyl)triethoxysilane (APTES)-functionalized M-MOF-74 (M-MOF-74-APTES, M = Zn, Cu or Mg) has been developed for the first time. It was found that even at the M-MOF-74-APTES amount of 0.5 wt%, the functionalized MOFs could still stabilize the n-hexane-water   mixture to construct Pickering emulsions. The as-generated Pickering emulsions could be efficiently demulsified upon bubbling of CO 2 , resulting in complete separation of oil and water phases, but could be restored by subsequent N 2 bubbling under homogenization. Mechanism study indicated that the acid-base reaction of CO 2 with the amino group of M-MOF-74-APTES resulted in the creation of hydrophilic salts, which led to the lowering of particle wettability and broke the stability of the emulsion, causing demulsification of the Pickering emulsion. After removing CO 2 , the emulsion can be reconstructed by the reversible reaction. As an applied example, the Pickering emulsion has been availed as a micro-reaction system and M-MOF-74-APTES as a carrier of Pd(OAc) 2 catalyst to realize the efficient combination of Suzuki-Miyaura reaction, product isolation and reuse of catalysts via alternate bubbling or removing of CO 2 .

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Small Methods · 2024 ·Vol. 8 ·期 12 ·2400143 · IF 10.7

AuBr3 Induces CsPb(Br/I)3 QDs to Self-Assemble into Nanowires

Shouying Mu,Ye He,YueLi Wang,Wei Chen,Chunyan Lv,Xiaojuan Liang,Weidong Xiang,Zhaopin Chen

Perovskite quantum dots can form various forms such as nanowires, nanorods, and nanosheets through self-assembly. Nanoscale self-assembly can be used to fabricate materials with excellent device properties. This study introduces AuBr 3 into CsPb(Br/I) 3 quantum dots, causing them to assemble into nanowires. The nanowires form because part of Au 3+ is surface-doped to replace Pb 2+ , and the [PbX6] 4− octahedral structure is distorted. The symmetry of the structural surface is broken, and a dipole-moment-induced field is generated, thus promoting self-assembly. Moreover, the presence of Au nanoparticles (NPs) causes a localized surface plasmon resonance and generates strong van der Waals forces that promote self-assembly. Finally, to test other applications of perovskite nanowires, the solution method is used to prepare films by compounding the sample solution and polystyrene (PS) for backlighted displays.

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TETRAHEDRON · 2017 · IF 2.651

Metal-free visible-light-promoted intermolecular [2+2]-cycloaddition of 3-ylideneoxindoles

Ling-Ling Wu,Gao H. Yang,Zhi Guan,Yan-Hong He

The Rose Bengal sensitized intermolecular [2 + 2]-cycloaddition of 3-ylideneoxindoles for the synthesis of spirocyclic oxindoles was developed successfully under visible light irradiation conditions. The cycloaddition products were obtained in good yields (up to 93%) with excellent diastereoselectivity and regioselectivity by using a low loading of Rose Bengal (0.125 mol%) as a triplet sensitizer. This work demonstrates the potential benefits of Rose Bengal in visible light catalysis.

CAS / MDL: 632-69-9
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JOURNAL OF MOLECULAR LIQUIDS · 2015 · IF 2.515

Densities and conductivities of seven 1-allyl-3-methylimidazolium carboxylate ionic liquids

Airong Xu,Yajuan Zhang,Zhiyong Li,Jianji Wang

In the present work, seven 1-allyl-3-methylimizodalium carboxylate ionic liquids (ILs), including 1-allyl-3-methylimizodalium formate [Amim][HCOO], acetate [Amim][CH 3 COO], propionate [Amim][CH 3 CH 2 COO], butyrate [Amim][CH 3 (CH 2 ) 2 COO], glycollate [Amim][HOCH 2 COO], lactate [Amim][CH 3 CHOHCOO]) and benzoate [Amim][C 6 H 5 COO], have been synthesized and characterized. Density ( ρ ) and conductivity ( σ ) have been determined experimentally for these ILs at 298.15   K and atmospheric pressure. Then molar volume ( V m ), standard entropy ( S °), lattice energy ( U POT ) and molar conductivity ( Λ ) of the ILs have been derived from the density and conductivity data. Ionicity of the ILs has been estimated using the Walden plot. Meanwhile, how anionic structure of the ILs affects the volumetric and conductivity properties of 1-allyl-3-methylimidazolium carboxylate ILs has been discussed from the analysis of structure–property relationship.

CAS / MDL: 107-05-1 107-92-6
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RSC Advances · 2016 ·Vol. 6 ·期 101 ·98761-98767 · IF 3.289

Synthesis, thermodynamic analysis and application of novel (3-(tert-butylperoxy)propyl)trimethoxysilane

Liqun Ma,Shaobo Dong,Zijian He,Yulin Yang,Hongge Jia,Yutao Di,Yanan Tang,Yazhen Wang

In order to develop a new silane coupling agent that can be used as coupling agent and initiator, (3-(tert-butylperoxy)propyl)trimethoxysilane was synthesized by using tert-butyl hydroperoxide and (3-chloropropyl) trimethoxysilane. The new reagent was characterized by 1H-NMR, FT-IR and mass spectroscopy. The thermokinetics of the new reagent was investigated, including thermal stability, decomposition constants (Kd), activation energy (Ea), the heat of decomposition (ΔH) and pre-exponential factor (Ad). In addition, the application of (3-(tert-butylperoxy)propyl)trimethoxysilane on modificating nano-TiO2 and initiating polymerization was studied. The structures of the products of modificating nano-TiO2 and initiating polymerization were verified by XPS, FT-IR. The results indicated that the new reagent had the characteristics of a coupling agent and initiator.

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ELECTROCHIMICA ACTA · 2017 · IF 4.798

Preparation of polypyrrole-coated Bi2O3@CMK-3 nanocomposite for electrochemical lithium storage

Wei Fang,Naiqing Zhang,Lishuang Fan,Kening Sun

Polypyrrole-coated Bi 2 O 3 @CMK-3 nanocomposite is prepared by nanocasting technique and chemical polymerization method. Bi 2 O 3 nanoparticles are dispersed into CMK-3 matrix, and polypyrrole is coated onto the surface of Bi 2 O 3 @CMK-3. Polypyrrole-coated Bi 2 O 3 @CMK-3 nanocomposite as an anode material for lithium-ion batteries has an outstanding power capability (321   mAh   g −1 at a current rate of 6   A   g −1 ) and a significantly improved cycling ability (380   mAh   g −1 after 1000 cycles at a current rate of 5   A   g −1 ). The greatly enhanced electrochemical performance of polypyrrole-coated Bi 2 O 3 @CMK-3 nanocomposite is associated with the synergistic effect of highly conductive CMK-3, polypyrrole layer and Bi 2 O 3 nanoparticles. Such a configuration inhibits the aggregation of Bi 2 O 3 nanoparticles and preserves the structure integrity of electrode material, in addition to highly improving the electrical conductivity and maintaining the stable structure of solid electrolyte interface film.

CAS / MDL: 109-97-7 657-84-1
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2016 ·Vol. 100 ·期 1 ·265-275 · IF 2.787

Ferroelectric to Relaxor Transition in BaTiO3–Bi(Zn2/3Nb1/3)O3 Ceramics

Longwen Wu,Xiaohui Wang,Zhengbo Shen,Longtu Li

The (1− x )BaTiO 3 – x Bi(Zn 2/3 Nb 1/3 )O 3 ( x = 0.01–0.30) ceramics were synthesized by solid-state reactions. The solubility limit was determined to be x = 0.20. A systematic structural transition from a tetragonal phase ( x ≤ 0.034), to a mixture of tetragonal and rhombohedral phases (0.038 ≤ x ≤ 0.20), and finally to a pseudocubic phase ( x ≥ 0.22) at room temperature was identified. Dielectric measurement revealed a ferroelectric ( x ≤ 0.04) to relaxor ( x ≥ 0.06) transition with permittivity peak broadening and flattening, which was further verified by Raman spectroscopy and differential scanning calorimetry (DSC). Activation energies obtained from the Vogel–Fulcher model displayed an increasing trend from ~0.03 eV for x ~ 0.05, to unusually high values (>0.20 eV) for the compositions with x ≥ 0.15. With the increase in Bi(Zn 2/3 Nb 1/3 )O 3 content, the polarization hysteresis demonstrated a tendency from high nonlinearity to sublinearity coupled with the reduction in remnant polarization and coervice field. The deconvolution of the irreversible/reversible polarization contribution was enabled by first-order reversal curve distributions, which indicates that the decreasing polarization nonlinearity with the increase in Bi(Zn 2/3 Nb 1/3 )O 3 concentration could be related with the change from the ferroelectric domain and domain wall contributions to the weakly coupled relaxor behaviors.

CAS / MDL: 513-77-9 13463-67-7
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RSC Advances · 2014 ·Vol. 4 ·期 81 ·42991-42995 · IF 3.708

Fe4[Fe(CN)6]3: a cathode material for sodium-ion batteries

He Sun,Haobo Sun,Wei Wang,Handong Jiao,Shuqiang Jiao

Insoluble Prussian blue (IPB), Fe4[Fe(CN)6]3, is synthesized at room temperature and found to achieve a relatively high storage capacity of 146 mA h g−1 (at a 20 mA g−1 rate) as the cathode material for Na-ion batteries with high potential plateaus. XRD, SEM and TEM are employed to characterize the morphology and microstructure of the as-synthesized IPB. First-principles calculation is introduced to study the electrochemical mechanism. Generally, the environmental friendliness and low cost of the material make it possible to be used for large-scale electric storage applications.

CAS / MDL: 7705-08-0 14434-22-1
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ELECTROCHIMICA ACTA · 2013 · IF 3.777

Electrochemical immunoassay platform for high sensitivity detection of indole-3-acetic acid

Yunlei Zhou,Zhenning Xu,Mo Wang,Xiaomeng Meng,Huanshun Yin

A label-free electrochemical immunosensor for sensitive detection of indole-3-acetic acid (IAA) was developed using gold nanoparticles (AuNPs) functionalized with horseradish peroxidase labeled immunoglobulins G (AuNPs-HRP-IgG) as signal amplification probe and rat monoclonal antibody against IAA as capture probe. AuNPs-HRP-IgG could be immobilized and through the interaction between 4-aminophenylboronic acid and a single N-glycosylation site, which exist in the CH2 domain of IgG. The electrochemical immunosensor was characterized by differential pulse voltammetry (DPV) in 0.1   M PBS (pH 7.4) containing Fe(CN) 6 3−/4− as redox probe. The decreased oxidation peak current of Fe(CN) 6 3−/4− was used to monitor the antibody–antigen interaction. The electrochemical immunosensor exhibited a linear range from 1   ×   10 −9 to 5   ×   10 −6 M with a limit of detection of 5.5   ×   10 −10   M (S/N   =   3). The proposed electrochemical immunosensor could well discriminate IAA from other phytohormones, such as gibberellin, abscisic acid and salicylic acid. In addition, IAA extracted from leaf of mung bean sprouts was detected using the developed immunosensor for evaluating its applicability, and the recovery was from 93.5% to 106.75%.

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