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101.
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A very sensitive electroanalytical method was employed to determine bergenin in phosphate buffer with a pH of 6.0, bergenin was accumulated at a 4-(2-pyridylazo)-resorcinol (PAR) polymer film modified glassy carbon electrode (GCE) surface under the condition of open-circuit. In the following anodic sweep from −0.4 to 0.8 V, bergenin adsorbed at the PAR polymer film modified electrode surface, was oxidized and yielded a sensitive oxidation peak at 0.595 V. Due to its unique structure and extraordinary properties, the PAR polymer film shows higher accumulation efficiency toward bergenin compared with a bare GCE. Hence, the amount of bergenin at the PAR polymer film modified GCE surface increases significantly, and finally the oxidation peak current improves greatly. The experimental conditions, such as supporting electrolyte, pH value, accumulation time and scan rate, were optimized for the measurement of bergenin, and a sensitive electroanalytical method was proposed for bergenin determination. The oxidation peak current varies linearly with the concentration of bergenin over the range of 2.0 × 10−7 to 1.2 × 10−5 mol/L, and the detection limit is 2.0 × 10−8 mol/L after 3 min open-circuit accumulation. The relative standard deviation of the same electrode in 10 successive scans is 1.8% for 1.0 × 10−6 mol/L bergenin and 2.1% for interelectrodes, indicating excellent reproducibility. This new method was successfully demonstrated with bergenin tablets and diluted urine. 相似文献
103.
Studyofthegrowthprocessofcolloidalparticlesofnonequilibriumandirreversibilityisanactiveareaofresearch.Therecognitionofcolloidalaggregatesasfractalobjectshasinspiredalargenumberofexperimentalandtheoreticalstudiesonthestructuralandkineticaspectsofaggregationprocesses"'.Morerecently,kineticsofhematiteaggregationbypolyacrylicacidhavebeenstudiedbyzhangandBume3.Theprimaryhematiteparticleswerequiteuniformandfairlyspherical.Inthispaper,wewillreportthesizeevolutionoffractalaggregatesofinitiallypolydis… 相似文献
104.
A simple method is developed to synthesize gram quantities of uniform Ge nanowires (GeNWs) by chemical vapor deposition on preformed, monodispersed seed particles loaded onto a high surface area silica support. Various chemical functionalization schemes are investigated to passivate the GeNW surfaces using alkanethiols and alkyl Grignard reactions. The stability of functionalization against oxidation of germanium for various alkyl chain lengths is elucidated by X-ray photoelectron spectroscopy. Among all schemes tested, long chain alkanethiols (> or = C12) are found to impart the most stable GeNW passivation against oxidation upon extended exposure to ambient air. Further, the chemically functionalized oxidation-resistant nanowires are soluble in organic solvents and can be readily assembled into close-packed Langmuir-Blodgett films potentially useful for future high performance electronic devices. 相似文献
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不同波长紫外光照下纳米TiO2薄膜的光致亲水性与循环伏安行为 总被引:6,自引:1,他引:6
通过溶胶-凝胶方法分别在ITO和玻璃表面制备了纳米TiO_2薄膜,研究了纳米 TiO_2薄膜在254及365nm的紫外光照射下的循环伏安行为和光致超亲水性。在紫外 光的照射下,TiO_2薄膜电极可表现出两个光电化学过程,纳米TiO_2薄膜的光致超 亲水性转变及两个光电化学过程的速率均取决于紫外光的波长,原因在于纳米 TiO_2薄膜对两种波长的光的吸收率和光子的能量不同。提出了光电化学过程的机 理,认为紫外光照射下纳米TiO_2薄膜的超亲水性变化与产生Ti~(3+)的过程引起的 表面微观结构变化存在的一定的内在联系。 相似文献
107.
以去离子水与乙二醇的混合液(体积分数分别为36.5%,48.7%,59.0%及71.2%,以下简称混合液)作为同轴传输线的绝缘介质,进行了μs级高电压负充电条件下的正电极击穿实验,研究了混合液的击穿电压、击穿时间、相对介电常数及电阻率与体积分数的关系。实验结果表明:在充电电压为20kV时,71.2%的混合液比36.5%的混合液的平均击穿电压提高25.1%,平均击穿时间延长10.49%,而相对介电常数减小868%。同时,随着充电时间的缩短,混合液的击穿电压提高。 相似文献
108.
109.
Inside Cover: High‐Nuclear Organometallic Copper(I)–Alkynide Clusters: Thermochromic Near‐Infrared Luminescence and Solution Stability (Chem. Eur. J. 49/2016) 下载免费PDF全文
110.
Dr. Xisen Hou Prof. Chenfeng Ke Dr. Yu Zhou Dr. Zhuang Xie Dr. Ahmed Alngadh Dr. Denis T. Keane Dr. Majed S. Nassar Dr. Youssry Y. Botros Prof. Chad A. Mirkin Prof. J. Fraser Stoddart 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(35):12301-12306
Covalent and supramolecular polymerizations, both of which offer their own unique advantages, have emerged as popular strategies for making artificial materials. Herein, we describe a concurrent covalent and supramolecular polymerization strategy—namely, one which utilizes 1) a bis‐azide‐functionalized diazaperopyrenium dication that undergoes polymeriation covalently with a bis‐alkyne‐functionalized biphenyl derivative in one dimension as a result of a rapid and efficient β‐cyclodextrin(CD)‐accelerated, cucurbit[6]uril(CB)‐templated azide–alkyne cycloaddition, while 2) the aromatic core of the dication is able to dimerize in a criss‐cross fashion by dint of π–π interactions, enabling simultaneous supramolecular assembly, resulting in an extended polymer network in an orthogonal dimension. 相似文献