Synthesis, structure, spectroscopic properties, and electrochemistry of (1,8,15,22-tetrasubstituted phthalocyaninato)lead complexes

Three (1,8,15,22-tetrasubstituted phthalocyaninato)lead complexes Pb[Pc(alpha-OR)(4)] [H(2)Pc(alpha-OC(5)H(11))(4) = 1,8,15,22-tetrakis(3-pentyloxy)phthalocyanine; H(2)Pc(alpha-OC(7)H(15))(4) = 1,8,15,22-tetrakis(2,4-dimethyl-3-pentyloxy)phthalocyanine; H(2)Pc(alpha-OC(10)H(7))(4) = 1,8,15,22-tetrakis(2-naphthyloxy)phthalocyanine] (1-3) have been prepared as racemic mixtures by treating the corresponding metal-free phthalocyanines H(2)Pc(alpha-OR)(4) (4-6) with Pb(OAc)(2).3H(2)O in refluxing n-pentanol. The molecular structure of Pb[Pc(alpha-OC(5)H(11))(4)] (1) in the solid state has been determined by single-crystal X-ray diffraction analysis. This compound, having a nonplanar structure, crystallizes in the monoclinic system with a P2(1)/c space group. Each unit cell contains two pairs of enantiomeric molecules, which are linked by weak coordination of the Pb atom of one molecule with an aza nitrogen atom and its neighboring oxygen atom from the alkoxy substituent of another molecule, forming a pseudo-double-decker supramolecular structure in the crystals with a short ring-to-ring separation, 2.726 A, and thus a strong ring-ring pi-pi interaction. The decreased molecular symmetry for these complexes has also been revealed by the NMR spectra of 1 and 2. The methyl protons of the 3-pentyloxy and 2,4-dimethyl-3-pentyloxy side chains of 1 and 2, respectively, are chemically inequivalent. In addition to the elemental analysis and various spectroscopic characterizations, these compounds have also been electrochemically studied. Two one-electron oxidations and up to five one-electron reductions have been revealed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods.     

EPR studies on H-abstraction from methylbenzenes by “magic blue” reagent

After mixing a methylbenzene 4 with “magic blue” solution in F113 (CClF₂CCl₂F) containing bis{perfluoro[1-(2-fluorosulfonyl)ethoxy]ethyl}nitroxide 2 and perfluoro-1-nitroso-1-[1-(2-fluorosulfonyl)ethoxy]ethane 3 at room temperature, benzylic H-atom of 4 could be selectively abstracted by 2, and benzyl radical 5 thus generated was immediately trapped by 3. Based on hyper-fine splitting constants (hfsc), the structure of the spin adducts perfluoro[1-(2-fluorosulfonyl)ethoxy]ethyl benzyl nitroxides 6 derived from seven methylbenzenes have been identified. The mechanism of the H-abstraction/spin trapping process is also discussed.     

Synthesis of oligo(p-phenylene vinylene)-porphyrin-oligo(p-phenylene vinylene) triads as antenna molecules for energy transfer

The oligo(p-phenylene vinylene)-porphyrin-oligo(p-phenylene vinylene) (P-OPVn, n=2, 4, where n is the number of phenyl rings) and the complex with Zn²⁺ based on P-OPVn were synthesized for investigating their photophysical properties via UV-vis, voltammetry, steady-state and time-resolved fluorescence spectra. In these molecules two OPV moieties as energy donors were linked to porphyrin center by virtue of Wittig reaction. The detailed studies of photophysical properties indicate that OPV group can act as an antenna unit for effective intramolecular energy transfer.     

Quantitative Determination of Three Protoberberine Alkaloids in Jin-Guo-Lan by HPLC-DAD

An accurate and simple HPLC method for the simultaneous determination of three protoberberine alkaloids (columbamine, jatrorrhizine, and palmatine) contained in Chinese medicine Jin-Guo-Lan (Tinospora sagittata Oliv. and Tinospora capillipes Gagnep) is presented in this study. The herb samples from six main origins and three herb markets were investigated. The separation was performed on a YMC-C₁₈ ODS column at 30°C with a gradient elution program. Acetonitrile and phosphate buffer (0.02 mol L⁻¹ sodium dihydrogen phosphate and 0.01 mol L⁻¹ triethylamine, pH 3) were used as mobile phases and the flow rate was set at 1 mL min⁻¹. The recovery of the method was in the range of 99.43–100.96%, and all the alkaloids showed good linearity (r ² > 0.9997) in the relatively wide concentration ranges. The developed method was applied to the determination of these alkaloids in the collected herb samples, and the results showed that the contents of these components in Jin-Guo-Lan varied greatly from habitat to habitat. It was demonstrated that the proposed method was helpful for the quality evaluation of Chinese medicine Jin-Guo-Lan.     

A combination chemical and enzymatic approach for the preparation of azole carboxamide nucleoside triphosphate

Alternative substrates for DNA and RNA polymerases offer an important set of biochemical tools. Many of the standard methods for nucleoside triphosphate synthesis fail in the cases of nonpurine and nonpyrimidine nucleosides. An efficient preparation of the 5'-O-tosylates for both the deoxy- and ribonucleosides enabled preparation of the diphosphate esters by displacement with tris(tetra-n-butylammonium) pyrophosphate. Enzymatic synthesis of the azole carboxamide deoxyribonucleoside triphosphate was based on ATP as the phosphate donor, nucleoside diphosphate kinase as the catalyst, coupled with phosphoenol pyruvate (PEP) and pyruvate kinase as an ATP regeneration system. Ribonucleoside triphosphate synthesis required PEP as the phosphate donor and pyruvate kinase as the catalyst. An optimized purification procedure based upon boronate affinity gel was developed to yield highly purified nucleoside triphosphates. The strategy outlined here provides a new and efficient method for preparation of nucleoside 5'-triphosphate and is likely applicable to a broad variety of base and sugar modified nucleoside analogues.     

Combined investigation of experimental characterization and theoretic calculation on the structure of dextran-Fe3O4 clusters

Dextran-Fe₃O₄ hybrid clusters were fabricated by coprecipitating ferric and ferrous ions in the presence of dextran, and after characterization of these clusters combined with calculation based on classical nucleation theory, a structure model of these hybrid clusters was proposed. The hybrid cluster was believed including small Fe₃O₄ nanoparticles and dextran which acted as both nucleating agent and stabilizer, so that exist in both the inside of magnetite nanoparticles and the periphery of the hybrid clusters. Besides, the effects of W_CD (weight_{iron cation}:weight_dextran) and molecular weight of dextran on the size, morphology and magnetic property of clusters were also investigated in this paper. It was found that the variation of W_CD and molecular weight of dextran have great effect on the size of the hybrid clusters, but have almost no effect on the size of the Fe₃O₄ nanoparticles. The characterization of magnetic property demonstrated that the Fe₃O₄ nanoparticles are of a single domain and the saturation magnetization was affected by the size of dextran-Fe₃O₄ hybrid clusters.     

土壤和沉积物石油污染现状

针对全球石油污染的现状从原油的组成、分类与对环境的潜在影响、原油中有毒有害物质的成分、石油的工业工艺流程等方面进行了论述,并着重分析了中国土壤和沉积物原油污染,对松辽盆地、济阳坳陷、塔里木盆地、渤海油区等区域污染现状作了详细介绍,对石油勘探开发中重要污染源之一——化学助剂造成的污染也作了总括.     

不同进风型式下气体冷却服中空气流动与换热的研究

根据气体冷却服的特点,对不同进风型式下气体冷却服中空气流动与换热进行研究。建立了进气口加设挡板层、进气口带均流器型和直吹型3种型式气体冷却服(服装夹层)中冷却空气流动过程的数学模型。对气体的流动过程进行分析,结果表明:不同的进风型式对气体冷却服空气层的温度分布状况、平均气流流速、平均温度、对流散热量影响较大;其中进气口加设挡板层的服装空气夹层温度分布最均匀,进气直吹型的平均气流流速最大,对流散热效果最好。研究结果为气体冷却服进一步的布风优化设计提供了理论和应用依据。     

基于反向传播神经网络的阻抗断层图像重建新方法

电阻抗成像是通过对物体表面电压、电流的测量来重建物体内部阻抗分布或变化图像的一种新颖计算机断层成像技术。阻抗断层图像重建是一种病态的、非线性的逆问题。提出了一种全新的阻抗断层图像重建方法，它利用反向传播神经网络来表征物体内部阻抗变化位置与物体表面电压变化大小的非线性映射关系，从而可以根据对物体表面测量电压的变化先准确定位阻抗变化区域，再用线性近似方法重建阻抗变化图像，这种方法不仅具有一定的抗噪能力，而且成像精度和空间分辨率都大大好于逆投影方法。     

激光烧蚀脉冲放电激发的土壤等离子体电子数密度和温度的研究

以激光烧蚀快脉冲放电激发土壤为例,研究了激光烧蚀快脉冲放电等离子体技术产生的土壤等离子体的电子数密度和温度。根据实验测得的Si原子和离子谱线的强度和萨哈玻尔兹曼方程,计算了等离子体的电子温度,并从分析Si I 250.69nm谱线的斯塔克展宽中导出了等离子体的电子数密度。与使用同样激光能量激发的激光等离子体相比,激光烧蚀快脉冲放电激发等离子体的电子数密度和温度都明显增加,与观察到的光谱信号强度是一致的。