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MICROCHIMICA ACTA · 2017 ·Vol. 184 ·期 4 ·1109-1116 · IF 4.58

Highly fluorescent carbon polymer dots prepared at room temperature, and their application as a fluorescent probe for determination and intracellular imaging of ferric ion

Xia Jie,Zhuang Yu-Ting,Yu Yong-Liang,Wang Jian-Hua

Carbon polymer dots (CPDs) were prepared by a one-pot aqueous synthetic route from ascorbic acid and diethylenetriamine at room-temperature. The CPDs under 350-nm excitation exhibit blue fluorescence peaking at 430 nm with a quantum yield of 47%. Other features include an average diameter of 5 nm, a fluorescence that is independent of the excitation wavelength, good water dispersibility and photostability, and excellent biocompatibility. The CPDs are shown to be viable fluorescent probes for ferric ion which acts as a strong quencher. The response to Fe(III) is linear in the 0.2 to 10 μM concentration range, and the detection limit is 0.1 μM. The probe was applied to the determination of Fe(III) in environmental waters and to intracellular imaging of ferric ions in HeLa cells. Carbon polymer dots (CPDs) are prepared from ascorbic acid and diethylenetriamine (DETA) at room-temperature (RT). The RT-CPDs exhibit excellent optical performance, biocompatibility and selectivity of quenching by ferric ions. This can be applied for determination and intracellular imaging of ferric ion.

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Journal of Analysis and Testing · 2017 ·Vol. 1 ·期 1 ·1-7 · IF 0

In Situ Growth of Flexible Polyphenylene-Conjugated Microporous Polymer Films for Fluorescence Detection of the Total Quantity of Developing Agents and Their Oxidation Products

Zhou Langjun,Peng Yi,Hu Yuling,Li Gongke

Conjugated microporous polymers (CMPs) are a kind of porous skeleton polymers, which are characterized by extended conjugated skeletons, large specific surface area and structure stability. In this work, a facile and versatile method was developed to fabricate flexible conjugated microporous polymer films for fast detecting the total quantity of developing agents and their oxidation products. Conjugated microporous polymer films were synthesized through in situ one-step approach by Suzuki coupling reaction. With such merits such as intense luminescence, easy synthesis and disposability, the polymer films were employed to detect developers based on fluorescence quenching in the printing wastewater. A linear response to p -benzoquinone, oxidation product of developers, was obtained in the range of 0.05–0.5 μmol·L −1 , with a detection limit of 0.015 μmol·L −1 . The strategy for in situ growth of flexible polyphenylene-conjugated microporous polymer (PP-CMP) films seems to be a very portable and general method for meeting different analytic purposes.

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Nanoscale Research Letters · 2017 ·Vol. 12 ·期 1 ·1-8 · IF 2.833

Effects of precursor solution composition on the performance and I-V hysteresis of perovskite solar cells based on CH3NH3PbI3-xClx

Zhang Z. L.,Men B. Q.,Liu Y. F.,Gao H. P.,Mao Y. L.

Precursor solution of CH 3 NH 3 PbI 3-x Cl x for perovskite solar cells was conventionally prepared by mixing PbCl 2 and CH 3 NH 3 I with a mole ratio of 1:3 (PbCl 2 :CH 3 NH 3 I). While in the present study, CH 3 NH 3 PbI 3-x Cl x -based solar cells were fabricated using the precursor solutions containing PbCl 2 and CH 3 NH 3 I with the mole ratios of 1:3, 1.05:3, 1.1:3, and 1.15:3, respectively. The results display that the solar cells with the mole ratio of 1.1:3 present higher power conversion efficiency and less I-V hysteresis than those with the mole ratio of 1:3. Based on some investigations, it is concluded that the higher efficiency could be due to the smooth and pinhole free film formation, high optical absorption, suitable energy band gap, and the large electron transfer efficiency, and the less I-V hysteresis may be attributed to the small low frequency capacitance of the device.

CAS / MDL: 546-68-9
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JOURNAL OF MATERIALS SCIENCE · 2016 ·Vol. 52 ·期 6 ·3321-3329 · IF 2.302

Transparent magnetic wood composites based on immobilizing Fe3O4 nanoparticles into a delignified wood template

Gan Wentao,Gao Likun,Xiao Shaoliang,Zhang Wenbo,Zhan Xianxu,Li Jian

Wood is one of the key renewable resources due to its excellent structure and physical properties. Functionalized wood and wood-based materials not only possess important engineering applications but also great potential in some new technology fields, such as electronics, optics, and energy. Endowing these functional wood-based materials with magnetic properties has an important significance for exploring lightweight building materials or electronic devices. In this study, we report the fabrication of a transparent magnetic wood (TMW) based on filling the index-matching methyl methacrylate and magnetic Fe 3 O 4 nanoparticles into the delignified wood template. The presence of the polymer and Fe 3 O 4 nanoparticles within the wood structure is monitored by scanning electron microscopy, energy-dispersive X-ray analysis, and Fourier transformation infrared spectroscopy. The resulting TMW possesses moderate transparency and magnetic properties combining with outstanding mechanical performance. Moreover, the influence of the concentration of Fe 3 O 4 nanoparticles on the final optical, magnetic, and mechanical properties of TMW is also discussed. This work provides a potential strategy to develop wood-based materials for magneto-optical application.

CAS / MDL: 1317-61-9 80-62-6
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Food Analytical Methods · 2016 ·Vol. 10 ·期 6 ·1653-1660 · IF 2.167

Selenium Speciation in Rice Samples by Magnetic Ionic Liquid-Based Up-and-Down-Shaker-Assisted Dispersive Liquid-Liquid Microextraction Coupled to Graphite Furnace Atomic Absorption Spectrometry

Wang Xiaojun,Chen Peng,Cao Liang,Xu Guoliang,Yang Siyu,Fang Ye,Wang Guozhen,Hong Xincheng

A novel and sensitive magnetic ionic liquid-based up-and-down-shaker-assisted dispersive liquid-liquid microextraction (MIL-UDSA-DLLME) was developed for the graphite furnace atomic absorption spectrometric measurement of inorganic selenium speciation from various rice matrixes. In the first microextraction step, the magnetic ionic liquid (1-butyl-3-methylimidazolium tetrachloroferrate, [C 4 mim][FeCl 4 ]) was selected to extract the complex of Se(IV) and 2,3-diaminonaphthalene from aqueous solution by the assistance of up-and-down-shaker vortex agitator. After the microextraction step, the magnetic ionic liquid containing target analytes was collected at the bottom of the tube by applying an external magnetic field around the test tube. Under the optimized conditions, the method present has low detection limit (0.018 μg L −1 ), wide linear dynamic range (0.03–10 μg L −1 ), and good repeatability (<3.0%, n  = 10) for Se(IV). The proposed methodology was applied for separation and preconcentration of inorganic selenium in standard reference materials including GBW10010 rice, GBW10043 Liaoning rice, and GBW10045 Hunan rice with satisfactory results. The developed methodology was also successfully used for the speciation of Se(IV) and Se(VI) in different rice samples with the relative recoveries within the acceptable range of 94.9–104.8% for the addition recovery tests.

CAS / MDL: 771-97-1
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2016 ·Vol. 28 ·期 5 ·4204-4210 · IF 1.798

Nb-doped BaTiO3–(Na1/4Bi3/4)(Mg1/4Ti3/4)O3 ceramics with X9R high-temperature stable dielectric properties

Huang Xuechen,Zhang Wenqin,Xie Juan,Xu Qi,Zhang Lin,Hao Hua,Liu Hanxing,Cao Minghe

Nb 2 O 5 doped 0.8BaTiO 3 –0.2(Na 1/4 Bi 3/4 )(Mg 1/4 Ti 3/4 )O 3 (0.8BT–0.2NBMT) polycrystalline ceramics were prepared by solid state reaction method. 0.8BT–0.2NBMT samples were observed to possess two dielectric peaks, which were attributed to the formation of core–shell structure (Huang et al. in J Eur Ceram Soc 36:533–540, 2015 ). Longer sintering induced uniform distributions of the additives. The introduction of Nb 2 O 5 into 0.8BT–0.2NBMT could obviously bring about the improvement of the dielectric temperature stability, the degradation of the dielectric loss at room temperature and the decrease of the sintering temperature. The 0.8BT–0.2NBMT ceramics doped with 2.0 at% Nb 2 O 5 could satisfy the temperature range of the X9R (−55 to 200 °C, △C/C 25°C  = ±15% or less) characteristics, with a moderate dielectric constant of 1130, low dielectric loss of 0.7%, low sintering temperature of 1050 °C and insulation resistivity of 5 × 10 12  Ω cm at room temperature, which might be promising for practical use in multilayer ceramic capacitors. The inhomogeneous distribution and the existence of the secondary phases were responsible for this excellent dielectric temperature characteristic. The complex impedance analysis was introduced to elaborate the conduction mechanism.

CAS / MDL: 497-19-8
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MICROCHIMICA ACTA · 2016 ·Vol. 183 ·期 9 ·2589-2595 · IF 4.831

Colorimetric determination of the activity of acetylcholinesterase and its inhibitors by exploiting the iodide-catalyzed oxidation of 3,3′,5,5′-tetramethylbenzidine by hydrogen peroxide

Ni Pengjuan,Sun Yujing,Dai Haichao,Jiang Shu,Lu Wangdong,Wang Yilin,Li Zhen,Li Zhuang

We describe a sensitive and selective colorimetric method for the determination of the activity of the enzyme acetylcholinesterase (AChE) and its inhibitors. Detection is based on the fact that acetylthiocholine iodide (ATCI) catalyzes the oxidation of the substrate 3,3′,5,5′-tetramethylbenzidine (TMB) by H 2 O 2 to form a blue product (ox-TMB) with an absorption peak at 652 nm, but that oxidation is suppressed if ACTI previously is hydrolyzed by AChE to form thiocholine which decolorizes ox-TMB. In the presence of inhibitor, the activity of AChE is inhibited, thereby inducing the recovery of the blue coloration. Based on these findings, a highly sensitive method is developed for the determination of AChE and its inhibitors. The assay only requires mixing of buffer, solutions of ATCI, TMB, H 2 O 2 and a sample containing AChE and photometric measurement. It works in the 0.05 to 5 mU•mL −1 enzyme activity range and has a detection limit as low as 30 μU•mL −1 . The inhibitor neostigmine causes 50 % enzyme inhibition in 14.5 nM concentration. This analytical system has a wide scope in that it may be applied to the determination of the activity of various other hydrolases with proper substrates. The blue product formed by the iodide-catalyzed oxidation of 3,3′5,5′-tetramethylbenzidine (TMB) by hydrogen peroxide is decolorized if acetylthiocholine iodide (ATCI) is hydrolyzed by acetylcholinesterase (AChE) to form thiocholine. If, however, AChE is inhibited, color formation will take place again.

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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2017 ·Vol. 409 ·期 17 ·4207-4213 · IF 3.431

Dual-mode immunoassay based on shape code and infrared absorption fingerprint signals of silica nanorods

Zhao Pengfei,Ni Ran,Wang Kexin,Hong Xia,Ding Yadan,Cong Tie,Liu Junping,Zhao Huiying

Silica nanorods were synthesized through a simple one-pot emulsion-droplet-based growth method, in which tetraethylorthosilicate (TEOS) was used as the silica source, ammonia as the catalyst, and polyvinylpyrrolidone (PVP) as the structure-directing agent and stabilizer. By controlling hydrolysis and condensation in the reaction process, we regulated the aspect ratios and the infrared (IR) absorption fingerprint signals (the transverse optical and the longitudinal optical phonon modes) of the silica nanorods. Based on this, a dual-mode immunoassay was performed for detecting model target analyte, human IgG. The shape code of the silica nanorods was used for simple, rapid qualitative, and sensitive semi-quantitative immunoassay by using a conventional optical microscope. The characteristic IR absorption fingerprint signals of the silica nanorods allowed for reliable quantitative immunoassay with good selectivity and high specificity. The detection limit and the linear range were found out to be 0.5 pM and 1 pM–10 nM, respectively. We expect that such dual-mode immunoassay could be applied for the detection of other analytes, such as protein, nucleic acids, bacteria, viruses, explosives, toxins, and so on. A simple dual-mode immunoassay was performed using the shape code and infrared absorption fingerprint signals of silica nanorods as detection signals.

CAS / MDL: 68-04-2 1077-28-7
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Nanoscale Research Letters · 2016 ·Vol. 11 ·期 1 ·1-9 · IF 2.584

Synthesis of Nitrogen and Sulfur Co-doped Carbon Dots from Garlic for Selective Detection of Fe3+

Sun Chun,Zhang Yu,Wang Peng,Yang Yue,Wang Yu,Xu Jian,Wang Yiding,Yu William W.

Garlic was used as a green source to synthesize carbon dots (CDs) with a systematic study of the optical and structure properties. Ethylenediamine was added into the synthesis to improve the photoluminescence quantum yield (PL QY) of the CDs. Detailed structural and composition studies demonstrated that the content of N and the formation of C–N and C=N were critical to improve the PL QY. The as-synthesized CDs exhibited excellent stability in a wide pH range and high NaCl concentrations, rendering them applicable in complicated and harsh conditions. Quenching the fluorescence of the CDs in the presence of Fe 3+ ion made these CDs a luminescent probe for selective detection of Fe 3+ ion.

CAS / MDL: 107-15-3
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2016 ·Vol. 408 ·期 10 ·2543-2555 · IF 3.125

Evaluation of synergistic enantioseparation systems with chiral spirocyclic ionic liquids as additives by capillary electrophoresis

Zhang Yanjie,Du Shuaijing,Feng Zijie,Du Yingxiang,Yan Zhi

In recent years, chiral ionic liquids (CILs) have attracted more and more attention in the field of enantioseparation. In this study, two novel spirocyclic chiral ionic liquids, 1-butyl-3-methylimidazolium(T-4)-bis[(2 S )-2-(hydroxy-κO)-3-methylbutanoato-κO]borate (BMIm + BLHvB − ) and 1-butyl-3-methylimidazolium (T-4)-bis[(α S )-α-(hydroxy-κO)-4-methylbenzeneacetato-κO]borate (BMIm + BSMB − ), were applied for the first time in capillary electrophoresis (CE) to establish synergistic systems for enantiomeric separation. Significantly improved separations of five tested analytes were observed in the CILs synergistic systems based on three β-cyclodextrin derivatives (CD), compared with conventional single CD separation systems. Several principal parameters such as CILs concentration, cyclodextrin concentration, buffer pH, and applied voltage were systematically investigated with BMIm + BLHvB − /hydroxypropyl-β-CD selected as a model system to optimize the enantioseparation. Molecular modeling was applied to further demonstrate the chiral recognition mechanism of the CILs/hydroxypropyl-β-CD synergistic system, which showed a good agreement with the experimental results.

CAS / MDL: 554-13-2 17199-29-0
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2016 ·Vol. 27 ·期 6 ·6188-6192 · IF 1.798

Synthesis and luminescence of spherical Y2O3:Eu3+ and Y2O3:Eu3+/Bi3+ particles

Wu Yeqiu,Jin Guangya,Liu Zhijian,He Tao

Y 2 O 3 :Eu 3+ and Y 2 O 3 :Eu 3+ /Bi 3+ particles with spherical morphology are synthesized by microwave-assistant hydrothermal process. The results show that cubic phase Y 2 O 3 :Eu 3+ and Y 2 O 3 :Eu 3+ /Bi 3+ particles with uniform size and spherical shape are obtained. The doping Eu 3+ and Bi 3+ ion have no influence on the phase and morphology of samples. In the hydrothermal process, the fast and homogeneous microwave heating benefits the formation of samples with uniform size and spherical shape. Both Y 2 O 3 :Eu 3+ and Y 2 O 3 :Eu 3+ /Bi 3+ show dominant red emission originating from the 5 D 0  →  7 F 2 transition of Eu 3+ . The codoping Bi 3+ can enhance the intensity of Eu 3+ emission.

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IONICS · 2016 ·Vol. 22 ·期 8 ·1377-1385 · IF 2.119

A novel nitroxide radical polymer-containing conductive polyaniline as molecular skeleton: its synthesis and electrochemical properties as organic cathode

Xu Lihuan,Ji Lvlv,Wang Guosheng,Zhang Cheng,Su Chang

A novel nitroxide radical-containing aniline, 4-(6-(2-amino-phenol-9 H -yl)hexanoyloxy)-2,2,6,6-tetramethylpiperidin-1-yloxy (AnT), was synthesized, and the copolymers of AnT and aniline (P (An-co-AnT)) were then prepared by chemical oxidative polymerization. The introduction of polyaniline (PAn) skeleton in copolymers improved the charge migration along polymer backbone, and the increased ratio of An/AnT monomer makes PAn’s anodic peak in copolymers shift to negative potential and the redox peaks for the nitroxide radical shift to the positive potential. Also, P (An-co-AnT) exhibited a gradually increased charged specific capacity from 120.1 to 141.0 mAh g −1 with increasing the feeding ratio of AnT/An, while the discharge specific capacity presented an opposite result. Specially, P (An-co-AnT) exhibited an obvious charge voltage platform and an even improved cycling stability than that of PAn in the high feeding ratio of AnT/An, and after 20 cycles, the discharge capacity of P (An-co-AnT) (1:1 ([An]/[AnT])) still maintained 82.7 % of the capacity obtained at the initial cycle.

CAS / MDL: 62-53-3 872-50-4 88-75-5
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