Transient Absorption Spectral Characterization of Electron Transfer between Fullerenes (C_(60)/C_(70)) and N,N,N′,N′-Tetra(p-methylphenyl)-4,4′-diamino-1,1′-diphenyl Sulphide (TPDAS)

Ｏｎｅｏｆｔｈｅｍｏｓｔｉｍｐｏｒｔａｎｔａｉｍｓｏｆｐｈｏｔｏｃｈｅｍｉｓｔｒｙｉｓｔｈｅｄｅｓｉｇｎａｎｄｃｏｎｓｔｒｕｃｔｉｏｎｏｆｍｏｌｅｃｕｌａｒｄｅｖｉｃｅｓｆｏｒｅｎｅｒ ｇｙｃｏｎｖｅｒｓｉｏｎａｎｄｉｎｆｏｒｍａｔｉｏｎｐｒｏｃｅｓｓｉｎｇ .Ｔｈｅｐｈｏｔｏａｃｔｉｖｅｍｏｌｅｃｕｌａｒｄｅｖｉｃｅｓａｒｅｂａｓｅｄｏｎｔｈｅｐｈｏｔｏｉｎｄｕｃｅｄｅｌｅｃｔｒｏｎｔｒａｎｓｆｅｒｂｅｔｗｅｅｎｄｏｎｏｒ ａｃｃｅｐｔｏｒｔｙｐｅｏｒｇａｎｉｃｃｏｍｐｏｕｎｄｓａｎｄａｃｃｅｐｔ…     

Quantitative analysis of nicotinic acid, nicotinamide and 3-cyanopyridine in industrial effluent by high performance liquid chromatography

A rapid and reliable high performance liquid chromatographic (HPLC) method for the simultaneous determination of heterocyclic compounds, namely nicotinic acid, nicotinamide, and 3-cyanopyridine, in industrial effluent is described. A Φ4.6 mm × 150 mm, 5 μm C-18 reversed phase stationery phase, and a methanol-acetonitrile-water tertiary mobile phase (20:20:60 v/v) were used for separation. The detection wavelength of a diode array (DAD) was set at 216 nm with a bandwidth of 16 nm. Phenol was used as an internal standard. The regression equations revealed a linear relationship between the concentration of the analytes injected and the peak area detected by DAD. The limits of detection (S/N = 3) ranged from 0.70 to 1.18 mg L⁻¹, the recoveries ranged from 87% to 102% and the precision expressed as % RSD intra-day and inter-day varied from 0.9 to 3.9 and 1.2 to 5.6, respectively. This method is rapid, sensitive and suitable for the monitoring of nicotinic acid, nicotinamide, and 3-cyanopyridine in effluent of related pharmaceutical manufacturing plants.     

A Novel Octahedral Hexasilver(I) Cluster: Ag_6[SSCN(n-C_4H_9)_2]_6

ＣｏｍｐｏｕｎｄｓｆｏｒｍｅｄｆｒｏｍＣｕ ,ＡｇａｎｄＡｕｗｉｔｈｄｉｔｈｉｏ ｌａｔｅｌｉｇａｎｄｓ ,ｓｕｃｈａｓｔｈｅｄｉａｌｋｙｌｄｉｔｈｉｏｃａｒｂａｍａｔｅ (ＤＴＣ) ,ｍｅｒｃａｐｔｏｔｈｉａｚｏｌｉｎｅ (ＨＭＴ)ａｎｄｄｉａｌｋｙｌｄｉｔｈｉｏｐｈｏｓｐｈａｔｅｓ(ＤＤＰ) ,ｈａｖｅｐｌａｙｅｄａｎｉｍｐｏｒｔａｎｔｒｏｌｅｉｎｔｅｃｈｎｏｌｏｇｙ .1Ｃｕ(Ｉ) Ｓｃｌｕｓｔｅｒｓａｌｓｏｈａｖｅｂｅｅｎｉｍｐｌｉｃａｔｅｄｉｎｂｉｏｌｏｇｙａｓａｎ ｔｉ ｏｘｉｄａｎｔｓ .2Ｔｈｅｃｕｂａｎ…     

Multiplicity of Solutions of the Weighted p-Laplacian with Isolated Singularity and Diffusion Suppressed by Convection

In this paper, the authors study the multiplicity of solutions to the weighted p-Laplacian with isolated singularity and di?usion suppressed by convection ?div(|x|^α|?u|^p?2?u) + λ 1/|x|^β |?u|^p?2?u · x = |x|^γg(|x|) in B \ {0} subject to nonlinear Robin boundary value condition |x|^α|?u|^p?2?u · ?n = A ? ρu on ?B,where λ > 0, B ? R^N(N ≥ 2) is the unit ball centered at the origin, α > 0, p > 1, β ∈ R, γ > ?N, g ∈ C([0,1]) with g(0) > 0, A ∈ R, ρ > 0 and ?n is the unit outward normal. The same problem with di?usion promoted by convection, namely λ ≤ 0, has already been discussed by the last two authors (Song-Yin (2012)), where the existence, nonexistence and classi?cation of singularities for solutions are presented. Completely di?erent from [Song, H. J. and Yin, J. X., Removable isolated singularities of solutions to the weighted p-Laplacian with singular convection, Math. Meth. Appl. Sci., 35, 2012, 1089–1100], in the present case λ > 0, namely the di?usion is suppressed by the convection, non-singular solutions are not only existent but also may be in?nite which vary according only to the values of solutions at the isolated singular point. At the same time, the singular solutions may exist only if the di?usion dominates the convection.     

6元素集合上T0拓扑总数的计算

文中证明了有限预序集与有限偏序集的一些性质,并基于有限集上的拓扑和其上预序的一一对应关系,利用这些性质通过对极小元和极大元个数进行分类讨论,以一种有别于计算机算法而又容易理解的计算方法得出6元素集合上的T₀拓扑总数为130023.     

Qualitative properties of pulsating fronts for reaction–advection–diffusion equations in periodic excitable media

In this paper, we study the pulsating fronts of reaction–advection-diffusion equations with two types of nonlinear term in periodic excitable media. Firstly, for the case with combustion nonlinearity, the unique front is proved to decay exponentially when it approaches the unstable limiting state. Secondly, for the degenerate monostable type nonlinearity, it is shown that the front with critical speed is unique, monotone and decays exponentially at negative end, while the fronts of noncritical speeds decay to zero non-exponentially.     

CONDUCTIVITY METHOD APPLIED TO THE STUDY OF INTERACTION BETWEEN ADSORBENT AND ADSORBATE I．ADSORPTION OF LOW CONCENYRATION OF FREE ACID BY REGENERABLE CHITIN

The adsorption of low concentration of free acid by regenerable chitin is followed by electric conductance determination.The effect of acid concentratioin,content of functioinal amino groups,and ionic strength on adsorption was discussed.Experimental results indicate that the active centre of regenerable chitin is the free amino groups on ist surface ,and that the rate of adsorption of free acid was found to be affected by two factors:the interaction between the adsorbent and the adsorbate in solution and that between the adsorbate molecules or ions in solution.     

二苯并噻吩亚砜的单晶结构及其π-π堆积作用理论研究

采用X射线衍射法测定二苯并噻吩亚砜单晶结构,发现晶体中二苯并噻吩亚砜分子以反平行三明治式的结构Ⅲ和反平行位移式的结构Ⅳ两种堆砌方式交替堆砌形成有序π-π堆积晶体。二苯并噻吩亚砜单晶结构属于三斜型,空间群为P1,晶体参数为:a=0.84712nm,b=0.94137nm,c=1.20380nm,α=97.866°,β=106.2630°,γ=96.437°,V=0.9014nm3,R1(全部数据)=0.0348和ωR2(全部数据)=0.0814。利用BHandH/6-31 G**方法计算了二苯并噻吩亚砜分子间的π-π堆积作用,Ⅲ和Ⅳ堆砌模式的π-π堆积效应作用能相当大,其计算值分别为-36.06kJ/mol和-39.83kJ/mol,电荷分布表明正负电荷匹配是稳定晶体π-π堆积体系的重要因素。     

Supramolecular isomerism in the hydrogen-bonded network of (5<Emphasis Type="Italic">R</Emphasis>,10<Emphasis Type="Italic">R</Emphasis>)-3,8-dihydroxy-5,10-diethoxy-5,10-dihydrochromeno[5,4,3-<Emphasis Type="Italic">cde</Emphasis>]chromene monohydrate

A new compound (5R, 10R)-3,8-dihydroxy-5,10-diethoxy-5,10-dihydrochromeno[5,4,3-cde]chromene monohydrate was obtained from 3,4-dihydroxybenzaldehyde in aerobic basic aqueous ethanol solution in the presence of manganese chloride and triethylamine and crystallized in orthorhombic P2₁2₁2₁ space group (denoted as 1). When 1 was recrystallized from aqueous methanol, it was transformed to another crystal (2) with the same composition but in P2₁/n space group. The drastic difference in the extensive hydrogen bond network makes 1 a 3D and 2 a 2D infinite supramolecular structure, respectively.     

Eu3+在Ba2TiSi2O8中的发光

The barium titano-silicate phosphors doped with Eu³⁺ were synthesized by high temperature solid state reaction. The structures of as-synthesized samples were characterized by powder XRD. The maximum peaks of emission spectra of Ba₂TiSi₂O₈ and Ba₂TiSi₂O₈∶Eu³⁺ were respectively located at 450 and 618 nm, coming from the transitions of charge-transfer bands of Ti⁴⁺-O^2- and forced electric-dipole transition ⁵D₀-⁷F₂ of Eu³⁺. The luminous mechanisms of Ba₂TiSi₂O₈ and Ba₂TiSi₂O₈∶Eu³⁺ were suggested. The effects of concentration of Eu³⁺ on the luminous performance of Ba₂TiSi₂O₈∶Eu³⁺ were also studied and the results showed that the optimum concentration of Eu³⁺ was 0.12 mol per mole of matrix.