8-aminoquinoline functionalized graphene oxide for simultaneous determination of guanine and adenine

The nanocomposite graphene oxide/8-aminoquinoline (GAQ) was prepared as modified electrode material for simultaneous determination of guanine and adenine. The prepared GAQ was characterized by SEM, TEM, FTIR, Raman, and UV-vis, which confirmed that the 8-aminoquinoline had been functionalized by covalent modification. The differential pulse voltammetry (DPV) proved the electrochemical properties of the GAQ, which exhibited good electrocatalytic activity and prominent synergistic effect for sensitive determination of guanine and adenine. The guanine and adenine both were detection by DPV showed good linearity with linear range covering 0.1–160 μM, and the detection limits (LOD) (S/N = 3) both were estimated to be 0.033 μM for guanine and adenine, respectively.     

Regulation of aggregation and morphology of cyanine dyes on monolayers via gemini amphiphiles

The aggregation of dyes is of considerable importance in relating to their functions and applications. In this paper, we have investigated the regulation on the aggregation and morphology of two cyanine dyes, 3,3'-disulfopropyl-4,5,4',5'-dibenzo-9-methylthiacarbocyanine triethylammonium salt (MTC) and 3,3'-disulfopropyl-4,5,4',5'-dibenzo-9-phenylthiacarbocyanine triethylammonium salt (PTC), using a series of gemini amphiphiles (bis(2'-heptadecyl-3'-ethylimidazolium)-1,n-alkane dibromide, abbreviated as Gn, n=2, 4, 6, 8, 10). It has been found that both of the dyes could be adsorbed onto the monolayers of the gemini amphiphiles through the electrostatic and pi-pi interaction and stacked into H- or J-aggregate. The spacer of the gemini amphiphile showed good control over the aggregation of MTC: H-aggregate was favored when gemini amphiphiles with short spacer were applied, while J-aggregation was preferred in the case of longer spacer. Only J-aggregate was observed for PTC on gemini monolayer, regardless of the structure of the gemini amphiphiles. Interesting morphologies were observed for all the gemini/dye complex monolayers. Network structure and nanofibers were formed for the gemini/MTC films transferred below the plateau surface pressure and close to the collapse pressure, respectively. The ability of the complex monolayers to form nanofibers strongly depended on the component amphiphiles, G2>G4>G6, and no nanofibers were observed for G8/MTC and G10/MTC after the collapse. Only squared domains were observed for gemini/PTC monolayers. When both G2 and G10 were mixed, an individual control of the gemini amphiphiles over the aggregation of MTC in the complex monolayers was observed. The relationship among the spacer, dye structure, and aggregation was revealed.     

Anderson型杂多酸作为催化剂在有机合成中的应用

Anderson型杂多酸（通式为[XM₆O₂₄]^n－）是一类具有特殊结构和性质的多金属-氧簇无机化合物,由于其分子结构易于化学修饰和可设计性以及其在材料、催化和医药等领域具有很高的应用价值,因此一直受到研究者们的广泛关注.近几年来,Anderson型杂多酸在催化有机氧化反应中的应用对于绿色催化过程的研究逐渐显露出非常重要的意义.本综述对Anderson型杂多酸在有机合成反应中的催化应用进行了相关的调研,根据Anderson型多金属氧酸盐的结构分类对这些工作进行了归纳概述与总结.这将为Anderson型杂多酸的催化应用以及为绿色催化的研究提供新的思路.     

Microstructured silicon created with a nanosecond neodymium-doped yttrium aluminum garnet laser

We produce microstructured silicon using frequency doubled, nanosecond Nd:YAG pulses in SF₆ gas. The micro-penitentes formed are up to 20 μm tall with a sulfur concentration of 0.5% near the surface. The infrared absorption is increased to near unity and extends well below the original bandgap far into the infrared. These data are similar to results reported by others using more complicated and less economical femtosecond titanium sapphire and picosecond and nanosecond excimer lasers.     

REGULARITY FOR NONLINEAR ELLIPTIC SYSTEMS WITH DINI COEFFICIENTS UNDER NATURAL GROWTH CONDITION FOR THE CASE：1〈m〈2

In this article,we consider interior regularity for weak solutions to nonlinear elliptic systems of divergence type with Dini continuous coefficients under natural growth condition for the case 1相似文献   

A friction contact stiffness model of fractal geometry in forced response analysis of a shrouded blade

To investigate the nonlinear vibration behavior of a shrouded blade with friction dynamic contact interface, a friction contact stiffness model is proposed to describe the friction force at different rough interfaces and different normal loads. In the proposed model, the friction contact interface is discretized to a series of friction contact pairs and each of them can experience stick, slip, or separate states. Fractal geometry is used to simulate the topography of contact surfaces. The contact stiffness is calculated using the Hertz contact theory and fractal geometry, which is related to contact interfaces parameters including normal load, roughness, Young??s modulus, and Poisson??s ratio. The trajectory tracking method is used to predict the friction force and it is not necessary to judge the transition condition among stick, slip, and separate states. It is suitable for complicated periodic motion of the contact interfaces. The forced response of a real shrouded blade is predicted using the proposed model and the multi-harmonic balance method. The effect of surface roughness, initial normal load, and contact area on the forced response of a shrouded blade is studied. It is shown that contact stiffness increases with normal load and fractal dimension. The resonant amplitude is sensitive to the initial normal load and contact surface roughness. The response can be influenced by the contact area, which is an important parameter for blade designers.     

5-芳基-2-呋喃甲酰基氨基硫脲类衍生物的合成及水溶液中 阴离子识别研究

合成了一系列未见文献报道的5-芳基-2-呋喃甲酰基氨基硫脲类衍生物, 通过1H NMR, IR, 元素分析确认了其结构. 并利用紫外-可见吸收光谱考查了它们在DMSO及DMSO/H2O溶液中与F－, Cl－, Br－, I－, CH3COO－, , 等阴离子的识别作用. 结果表明: 该类受体分子能较好地识别F－, CH3COO－, 三种阴离子, 当加入这三种阴离子后, 溶液的颜色由淡黄色转变为亮黄色. 通过改变含水量可有效地调控识别作用的选择性. 1H NMR滴定实验进一步证实了受体分子与阴离子通过氢键作用形成主客体配合物.     

Computing communities in complex networks using the Dirichlet processing Gaussian mixture model with spectral clustering

Community detection becomes a significant tool for the complex network analysis. The study of the community detection algorithms has received an enormous amount of attention. It is still an open question whether a highly accurate and efficient algorithm is found in most data sets. We propose the Dirichlet Processing Gaussian Mixture Model with Spectral Clustering algorithm for detecting the community structures. The combination of traditional spectral algorithm and new non-parametric Bayesian model provides high accuracy and quality. We compare the proposed algorithm with other existing community detecting algorithms using different real-world data sets and computer-generated synthetic data sets. We show that the proposed algorithm results in high modularity, and better accuracy in a wide range of networks. We find that the proposed algorithm works best for the large size of the data sets.     

X-ray crystal structures ofcis-bis(diphenylphosphinamide)tetracarbonylmolybdenum(0) andtrans-bis(N-methyl diphenylphosphinamide)tetracarbonylmolybdenum(0)

The X-ray crystal structures ofcis-Mo(CO)₄(Ph₂PNH₂)₂,I, andtrans-Mo(CO)₄(Ph₂PNHMe)₂,II, are presented. ComplexI crystallizes in the monoclinic space groupP2₁/c(a=13.433(1),b=12.2719(8),c=17.318(2)Å;=109.79(1)°;V=2686.1(8)ų;Z=4). ComplexII crystallizes in the triclinic space groupP¯1 (a=6.9986(8),b=10.328(1),c=11.241(2)Å,=107.58(1)°,=91.76(1)°, =101.28(1)°,V=756.1(4)ų,Z=1). The molybdenum coordination geometry in each complex is a slightly distorted octahedron. The molybdenum-carbon bond lengths for the carbonyls trans to phosphorus in complexI are shorter than those the carbonyls trans to other carbonyls. The average molybdenum-phosphorus distance inI (2.525(5)Å) is similar to those in other diphenylphosphinamide complexes and longer than the molybdenum-phosphorus distance inII in 2.4585(7)Å). The distance between two nitrogen atoms incis Mo(CO)₄(Ph₂PNH₂)₂ (3.74(3)Å) is significantly larger than the sum of their van der Waals radii (3.10 Å) indicating that the two nitrogens are not hydrogen bonded.     

浅谈全息照相实验教学

为了提高全息照相实验的成功率和学生学习的积极性,本文从实验原理入手,分析了影响实验的诸因素,并提出了具体的解决方法。