四价锗与3, 4－二羟墓苯甲醛配合物的极谱研究

本文采用极谱法研究了Ge(Ⅳ)-3,4-二羟基苯甲醛(DHB)配合物的组成,条件稳定常数.并对该配合物的极谱波性质进行了研究.     

镉—溴化物—罗丹明B高灵敏显色反应的研究：离心光度法测定镉

本研究了一个高灵敏的测定镉的方法，离心光度法，该体系络合物λｍａｘ＝５６０ｎｍ，表观摩尔吸系数ε５６０＝５．０６×１０＾８Ｌ．ｍｏｌ＾－１．ｃｍ＾－１，Ｃｄ＾２＋浓度０．１０×１０＾－２－１．０×１０＾－２μｇ／１０ｍＬ呈线性关系，本法已用于血清和水中痕量镉的测定，探讨了高灵敏的显色反应机理。     

酞菁锰-表面活性剂薄膜电极的电化学表征及其对三氯乙酸的电化学催化作用的研究

将酞菁锰（ＭｎＰｃ）掺入阳离子表面活性剂双十二烷基二甲基溴化铵（ＤＤＡＢ）的氯仿溶液，并涂布于热解石墨电极表面，待氯仿挥发后即制得ＭｎＰｃ－ＤＤＡＢ薄膜电极。循环伏安实验表明，在ＫＢｒ溶液中，该薄膜电极有两对还原氧化峰，第一对峰的Ｅｐｃ１＝－０．２７Ｖ，Ｅｐａ１＝０．０１Ｖ；第二对峰的Ｅｐｃ２＝－０．７６Ｖ，Ｅｐａ２＝－０．６２Ｖ（ｖｓ．ＳＣＥ）。本文着重探讨了第二对峰的电化学行为，估计了该体系的电荷传递扩散系数Ｄｃｔ和表观非均相电极反应速率常数Ｋ０′等电化学参数，并可将该薄膜电极用于催化三氯乙酸的电化学还原。     

Carbon nanotube assisted synthesis of CeO2 nanotubes

CeO₂ nanotubes have been synthesized facilely using carbon nanotubes (CNTs) as templates by a liquid phase deposition method. The properties of the CeO₂ nanotubes were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectrum (XPS) as well as thermogravimetry and differential thermal analysis (TG-DTA). The obtained CeO₂ nanotubes with a polycrystalline face-centered cubic phase have a uniform diameter ranging from 40 to 50 nm. The CeO₂ nanotubes are composed of many tiny interconnected nanocrystallites of about 10 nm in size. The pretreatment of CNTs and calcination temperature were confirmed to be the crucial factors determining the formation of CeO₂ nanotubes. A possible formation mechanism has been suggested to explain the formation of CeO₂ nanotubes.     

A new C21-steroidal glycoside from Cynanchum stauntonii

A new C21-steroidal glycoside with two known compounds were isolated from the root of Cynanchum Stauntonii.Based on thespectral analysis,including MS,1H NMR,13C NMR,DEPT,1H-1H COSY,13C-1H COSY,HMQC and HMBC,their chemicalstructures were determinated as glaucogenin-C 3-O-a-L-cymaropyranosyl-(1→4)-b-D-digitoxopyranosyl-(1→4)-β-D-canaropyranoside(1),stigmasterol(2)and ursolic acid(3).     

24-亚甲基-胆甾-3β,5α,6β,19-四醇——一种罕见的含19-羟基的多羟基甾醇

从我国西沙群岛采集的软珊瑚Nephthea albida和南沙群岛采集的N.tixiexae uer seueldt的乙醇,抽提物中,通过硅胶层析分离出一种罕见的含19-羟基的多羟基甾醇——Nephalsterol-A(1),该物质为无色针状结晶,m.p.242～243℃,[a]_D~(20)=O(C 0.053,CH_3OH),为一新化合物。 (1)的ELMS显示分子离子峰m/z 448,结合~(13) NMR DEPT谱确定(1)的分子式为C_(28)H_(48)     

Highly efficient visible-light photocatalytic ethane oxidation into ethyl hydroperoxide as a radical reservoir

Photocatalytic ethane conversion into value-added chemicals is a great challenge especially under visible light irradiation. The production of ethyl hydroperoxide (CH₃CH₂OOH), which is a promising radical reservoir for regulating the oxidative stress in cells, is even more challenging due to its facile decomposition. Here, we demonstrated a design of a highly efficient visible-light-responsive photocatalyst, Au/WO₃, for ethane oxidation into CH₃CH₂OOH, achieving an impressive yield of 1887 μmol g_cat⁻¹ in two hours under visible light irradiation at room temperature for the first time. Furthermore, thermal energy was introduced into the photocatalytic system to increase the driving force for ethane oxidation, enhancing CH₃CH₂OOH production by six times to 11 233 μmol g_cat⁻¹ at 100 °C and achieving a significant apparent quantum efficiency of 17.9% at 450 nm. In addition, trapping active species and isotope-labeling reactants revealed the reaction pathway. These findings pave the way for scalable ethane conversion into CH₃CH₂OOH as a potential anticancer drug.

Highly efficient visible-light driven photocatalytic oxidation of ethane into ethyl hydroperoxide was realized for the first time over Au/WO₃.     

Geometries and properties of bimetallic phosphido-bridged complex Cp(CO)2W(μ-PPh2)W(CO)5 and Cp(CO)3W(μ-PPh2)W(CO)5

Complete geometry optimizations were carried out by HF and DFT methods to study the molecular structure of binuclear transition-metal compounds (Cp(CO)₃W(μ-PPh₂)W(CO)₅) (I) and (Cp(CO)₂W(μ-PPh₂)W(CO)₅) (II). A comparison of the experimental data and calculated structural parameters demonstrates that the most accurate geometry parameters are predicted by the MPW1PW91/LANL2DZ among the three DFT methods. Topological properties of molecular charge distributions were analyzed with the theory of atoms in molecules. (3, −1) critical points, namely bond critical point, were found between the two tungsten atoms, and between W1 and C10 in complex II, which confirms the existence of the metal–metal bond and a semi-bridging CO between the two tungsten atoms. The result provided a theoretical guidance of detailed study on the binuclear phosphido-bridged complex containing transition metal–metal bond, which could be useful in the further study of the heterobimetallic phosphido-bridged complexes.     

Hydrothermal Synthesis and Structural Characterization of a Tubular Arsenic-Vanadate: [CoII(2,2′-bpy)2]2[AsIII8VIV14O42(H2O)]·H2O

The hydrothermal reaction of VOSO₄, As₂O₃, CoC₂O₄·2H₂O and 2,2-bipy yields a novel arsenic-vanadate [Co^II(2,2-bpy)₂]₂[As^III₈V^IV ₁₄O₄₂(H₂O)]·H₂O (1), which is characterized by IR, elemental analysis, TGA, magnetic susceptibility and single crystal X-ray diffraction analysis. X-ray diffraction shows that compound 1 is the first example of tubular arsenic–vanadium cluster containing infinite {[Co(2,2-bpy)₂]₂[As₈V₁₄O₄₂(H₂O)]} chain constructed from [As₈V₁₄O₄₂(H₂O)] clusters interconnected through [Co(2,2-bpy)]²⁺ units. Crystal data: 1, orthorhombic, P 2₁2₁2₁, a=12.1401(2) Å, b=15.8722(1) Å, c=39.9533(5) Å, Z=4.Graphical Abstract: A novel polyoxoarsenicvanadate, [Co^II(2,2-bipy)₂]₂ [As^III₈V^IV ₁₄O₄₂(H₂O)]·H₂O, is depicted along with a tubular hybrid solid with a rhombic tube formed within the chain.     

米非司酮的吸附伏安特性

在ＰＨ７．０Ｂｒｉｔｔｏｎ－Ｒｏｂｉｎｓｏｎ缓冲溶液中，米非司酮（Ｍｉｆｅｐｒｉｓｔｏｎｅ，ＲＵ４８６）在汞电极上有２个不可逆的线性扫描还原峰，峰电位分别为－１．２３Ｖ和－１．６８Ｖ。本文探讨了第一峰的电化学行为。