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231.
Guangping Wan Hongjun Xia Jun Wang Jiawei Liu Botao Song Ying Yang Quan Bai 《中国化学快报》2018,29(1):213-216
The monodisperse superficially porous core-shell silica microspheres (CSSMs) with controllable shell thickness and pore size were synthesized by an improved polymerization-induced colloid aggregation (PICA) approach for fast separation of small solutes and proteins. 相似文献
232.
Hongbiao Du Guoyi Duan Nan Wang Jia Liu Yang Tang Ran Pang Yongmei Chen Pingyu Wan 《Journal of Solid State Electrochemistry》2018,22(12):3799-3806
Owing to its high oxygen evolution potential, PbO2 electrode is one of the candidates for electrochemical advanced oxidation processes (EAOPs). To further improve its performance as EAOP electrode, a Ga2O3-doped PbO2 electrode (Ga2O3–PbO2 electrode) was fabricated by the composite plating method. SEM and XRD results showed that the crystalline in the coating of Ga2O3–PbO2 electrode is more uniform and in smaller size than that in the undoped PbO2 electrode, which provided a higher specific surface area. The electrochemical studies showed that the Ga2O3–PbO2 electrode had higher oxygen evolution potential (OEP) and smaller electrode surface impedance, which is a benefit for the formation of hydroxyl radicals (·OH). The electrochemically degradation test using bromocresol green sodium (BG) solution and glucose solution as the simulated wastewater showed that the kinetics of electrochemical catalytic degradation is a pseudo-first-order reaction, and the reaction rate constant on Ga2O3–PbO2 electrode was 2 times accelerated. 相似文献
233.
Efficient Synthesis of Five Types of Heterocyclic Compounds via Intramolecular Elimination Using Ultrasound‐Static Heating Technique 下载免费PDF全文
Dr. Hongfei Jiang Xueyang Dong Xin Jin Danyang Zhu Dr. Ruijuan Yin Dr. Rilei Yu Prof. Shengbiao Wan Prof. Lijuan Zhang Prof. Tao Jiang 《化学:亚洲杂志》2018,13(16):2009-2013
An experimental technique, ultrasound‐static heating, has been developed for the efficient synthesis of heterocyclic compounds. The technique involves ultrasonic irradiation and static heating processes. First, the ultrasonic irradiation process is performed to form an intermediate of the heterocyclic compound under mild conditions and the subsequent static heating process (heating the intermediate under solvent‐free conditions without stirring) produces the target heterocyclic compounds via intramolecular elimination. 相似文献
234.
From Metal–Organic Frameworks to Single‐Atom Fe Implanted N‐doped Porous Carbons: Efficient Oxygen Reduction in Both Alkaline and Acidic Media 下载免费PDF全文
Long Jiao Gang Wan Rui Zhang Dr. Hua Zhou Prof. Dr. Shu‐Hong Yu Prof. Dr. Hai‐Long Jiang 《Angewandte Chemie (International ed. in English)》2018,57(28):8525-8529
It remains highly desired but a great challenge to achieve atomically dispersed metals in high loadings for efficient catalysis. Now porphyrinic metal–organic frameworks (MOFs) have been synthesized based on a novel mixed‐ligand strategy to afford high‐content (1.76 wt %) single‐atom (SA) iron‐implanted N‐doped porous carbon (FeSA‐N‐C) via pyrolysis. Thanks to the single‐atom Fe sites, hierarchical pores, oriented mesochannels and high conductivity, the optimized FeSA‐N‐C exhibits excellent oxygen reduction activity and stability, surpassing almost all non‐noble‐metal catalysts and state‐of‐the‐art Pt/C, in both alkaline and more challenging acidic media. More far‐reaching, this MOF‐based mixed‐ligand strategy opens a novel avenue to the precise fabrication of efficient single‐atom catalysts. 相似文献
235.
Two water‐soluble 6‐(pyrazin‐2‐yl)‐1,3,5‐triazine‐2,4‐diamino (pzta)‐based Cu(II) complexes, namely [Cu(l ‐Val)(pzta)(H2O)]ClO4 ( 1 ) and [Cu(l ‐Thr)(pzta)(H2O)]ClO4 ( 2 ) (l ‐Val: l ‐valinate; l ‐Thr: l ‐threoninate), were synthesized and characterized using elemental analyses, molar conductance measurements, spectroscopic methods and single‐crystal X‐ray diffraction. The results indicated that the molecular structures of the complexes are five‐coordinated and show a distorted square‐pyramidal geometry, in which the central copper ions are coordinated to N,N atoms of pzta and N,O atoms of amino acids. The interactions of the complexes with DNA were investigated using electronic absorption, competitive fluorescence titration, circular dichroism and viscosity measurements. These studies confirmed that the complexes bind to DNA through a groove binding mode with certain affinities (Kb = 4.71 × 103 and 1.98 × 103 M?1 for 1 and 2 , respectively). The human serum albumin (HSA) binding properties of the complexes were also evaluated using fluorescence and synchronous fluorescence spectroscopies, indicating that the complexes could quench the intrinsic fluorescence of HSA in a static quenching process. The relevant thermodynamic parameters revealed the involvement of van der Waals forces and hydrogen bonds in the formation of complex–HSA systems. Finally, molecular docking technology was also used to further verify the interactions of the complexes with DNA/HSA. 相似文献
236.
This article reports another step in an ongoing effort to understand the fragmentation of T-rich oligodeoxynucleotides. We extended an earlier investigation of T-rich 4-mers to T-rich 6-mers, 8-mers and 10-mers by using four different tandem mass spectrometric methods. The methods include low-energy collisionally activated decomposition (CAD) of electrospray ionization (ESI)-produced ions, source-CAD of ESI-produced ions, post-source decay (PSD), and CAD of matrix assisted laser desorption ionization (MALDI)-generated ions. The most abundant fragment ions produced from [M - 2H]2- precursors upon low-energy CAD in an ion trap are the [a - B]- and their complementary w ions. The predominant cleavage sites for T-rich oligodeoxynucleotides are always the 3' C-O bonds adjoining a non-T nucleobase (i.e., a base with a higher proton affinity (PA) than that of T). The relative abundance of [a - B]- correlates with the PAs of the nucleobases, underscoring the importance of proton transfer to the base. The propensity to form [a - B]- ions falls in the order of G > C approximately A > T. Structural isomers up to 10-mers can be readily sequenced and distinguished with each of the four tandem mass spectrometric methods applied. The fragmentation of oligodeoxynucleotides in which various phosphates were replaced with methylphosphonate is a measure of the participation of the phosphate proton in the formation of [a - B] ions. For 4 and 5-mers, transfer of an acidic proton from the 5'-phosphate to the departing base is the initiating step in the formation of [a - B]- ions. 相似文献
237.
Fe-Al-Mg-MMH/钠质蒙脱土分散体系触变性研究 总被引:3,自引:0,他引:3
研究了Fe-Al-Mg型混合金属氢氧化物(简称MMH)/钠质蒙脱土(简称MT)分散体系的触变性,发现在不同MMH/MT质量比(R)条件下,分散体系可分别呈现正触变性和负触变性.在所研究的R范围(0~0.091)内,随R增大,体系的触变性发生正触变性-复合触变性-负触变性的转化.考察了高速剪切分散后,测定粘度变化前的静置时间(ts)和测定粘度时的剪切速率(DL)对触变性的影响.探讨了各种触变性产生的原因,提出了“分散粒子-空间连续网络结构-密实聚集体”和“分散粒子-密实聚集体-密实聚集体簇”机理,较合理地解释了观察到的复合触变现象. 相似文献
238.
239.
The separation of the basic drug lidocaine and six of its metabolites has been investigated both by using volatile aqueous electrolyte system, at low pH and by employing non-aqueous electrolyte systems. In aqueous systems, the best separation of the compounds under the investigated conditions was achieved by using the electrolyte 60 mM trifluoroacetic acid (TFA)/triethylamine (TEA) at pH 2.5 containing 15% methanol. With this electrolyte, all seven compounds were well separated with high efficiency and migration time repeatability. The separations with bare fused-silica capillaries and polyacrylamide-coated capillaries were compared with higher separation efficiency with the latter. On the other hand, near baseline separation of all the seven compounds was also obtained by employing the non-aqueous electrolyte, 40 mM ammonium acetate in methanol and TFA (99:1, v/v), with comparable migration time repeatability but lower separation efficiency relative to the aqueous system. 相似文献
240.
A method for coating capillaries for capillary electrophoresis with chemically bonded polydimethylacrylamide has been developed, and the properties of the capillaries have been evaluated. The coated capillaries provided high separation efficiency, 12 x 10(5) theoretical plates/m was obtained for cytochrome c. The electroosmotic flow at pH 8.0 was 10 x 10(-10) to 6 x 10(-10) m2 V(-1) s(-1). The coated capillaries were quite stable at high pH. At least 150 runs could be done at pH 10 without appreciable performance deterioration. The excellent performance of the coated capillaries was illustrated by separation of basic proteins, acidic proteins, 9-fluorenylmethyl chloroformate-derivatized neurotransmitter amino acids, peptide reference mixtures and peptides digested from a bacteria protein. 相似文献