A Novel Approach to Synthesis of Tricyclic Diterpenoid

A novel approach has been found and the first total synthesis of (±)-Salvirecognine was accomplished by using it. In which intramolecular cyclization and Friedel-Crafts alkylation took place simultaneously to afford key intermediates for synthesis of aromatic tricyclic diterpenoids OMe PPA O O O OMe 1 2 Scheme 1 As shown in Scheme 1 intramolecular cyclization and Friedel-Crafts alkylation took place simultaneously when compound 1 was treated by PPA at 125 ℃. In which the i-pr…     

Moisture absorption and absorption kinetics in polyelectrolyte films: influence of film thickness

Specular X-ray reflectivity (XR) and quartz crystal microbalance (QCM) measurements were used to determine the absorption of water into thin poly(4-ammonium styrenesulfonic acid) films from saturated vapor at 25 degrees C. The effect of film thickness on the absorption kinetics and overall absorption was investigated in the range of thickness from (3 to 200) nm. The equilibrium swelling of all the films irrespective of film thickness was (0.57+/-0.03) volume fraction. Although the equilibrium absorption is independent ofthickness, the absorption rate substantially decreases for film thickness < 100 nm. For the thinnest film (3 nm), there is a 5 orders of magnitude decrease in the diffusion coefficient for water.     

混合配体、希土三元配合物的研究 Ⅳ.3,5二硝基水扬酸(H2DNSA)、邻菲咯啉(phen)、希土(RE)三元固体配合物的合成及性质

本文报道了十种希土元素与3,5-二硝基水扬酸、邻菲咯啉三元配合物的制备方法。通过元素和化学分析测定了化合物的化学组成,并用红外光谱、紫外光谱、差热分析、磁化率、X射线粉天衍射等对所合成的化合物进行了结构和性质的研究。     

FeZSM－5沸石上乙苯的吸附态及氧化脱氢

ＦｅＺＳＭ－５吸附乙苯前后的ＩＲ、ＸＰＳ、ＥＳＲ及Ｍｏｓｓｂａｕｅｒ谱表明，乙苯分子的侧链和苯环与ＦｅＺＳＭ－５的活性位（以Ｆｅ为中心的结构单元）同时发生配位络合作用，减弱了乙苯分子侧链的α和β位Ｃ－Ｈ键，使其活化，在氧存在下易发生氧化脱氢反应生成苯乙烯．Ｆｅ（Ⅲ）是乙苯氧化脱氢的活性中心，尤其是骨架不饱和配位的Ｆｅ（Ⅲ）对活化乙苯分子起到了关键作用，碱金属平衡阳离子起到了助催化剂的作用．骨架Ｆｅ（Ⅲ）比非骨架Ｆｅ（Ⅲ）具有更高的氧化脱氢活性     

QSPR-based prediction of adsorption of halogenated aromatics on yellow-brown soil

Halogenated aromatic compounds exist widely in soil and aqueous environment. The study of their transport and distribution is quite important for pollution control and risk assessment. In the present work the adsorption coefficients of 28 halogenated benzenes, anilines and phenols on yellow-brown soil were measured with batch equilibrium method, and a prediction model was developed through the quantitative structure-property relationship (QSPR) technique. Then the obtained model was tested with Monte Carlo simulation and Jacknife methods. The results indicated that it was robust enough to estimate soil adsorption behaviors for the tested compounds. Based on the obtained model it could be deduced that the adsorption of halogenated aromatics on yellow-brown soil was not a simple partitioning process but involved complicated interactions.     

均匀棒状过氧化氢合碳酸钠制备及非等温热分解动力学

本文制备了均匀棒状过氧化氢合碳酸钠，化学分析确定其组成为Na₂CO₃·1.5H₂O₂，用DTA-TG-DTG技术并辅以X-ray分析研究了它在静态空气、流动氧气和流动氮气气氛中的非等温热分解过程及动力学。     

Enhancement of three-photon absorption cross-sections in a novel class of symmetrical charge transfer fluorene-based molecules

The three-photon absorption effect (3PA) of two novel symmetrical charge transfer fluorene-based molecules (abbreviated as BASF and BMOSF) has been determined by using a Q-switched Nd:YAG laser pumped with 38 ps pulses at 1064 nm in DMF. The measured 3PA cross-sections are 84 × 10⁻⁷⁸ and 114 × 10⁻⁷⁸ cm⁶ s², respectively. The geometries and electronic excitations of these two molecules are systematically studied by PM3 and ZINDO/S methods. The relationships between 3PA cross-sections and intramolecular charge transfer are discussed micromechanically. The experimental and theoretical results have shown that the larger intramolecular charge transfer, which was characterized by the charge density difference between the ground state (S₀) and the first excited state (S₁), the greater enhancement of the 3PA cross-sections.     

Surprising selectivity in the transformation of dimethoxy azaindoles

Transformation of 4,7-dimethoxy-6-azaindole into 4-hydroxy-7-methoxy-6-azaindole or 7-hydroxy-4-methoxy-6-azaindole can be readily controlled by careful selection of a reagent. Treatment with concentrated HCl results in hydrolysis at the 4-position exclusively, while TMS-I provides demethylation at the 7-position only. Products were unambiguously identified by single crystal X-ray crystallography.     

Sonochemical synthesis of mass single-crystal PbS nanobelts

Based on sonochemical technique, large-scale PbS nanobelts are successfully synthesized in the mixed solution of PbCl₂ and Na₂S₂O₃. These nanobelts are characterized using X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), selected area electronic diffraction, energy dispersive X-ray spectroscopy, and high-resolution TEM. The as-synthesized PbS nanobelts have width of about 80 nm, length up to several millimeters, and width-to-thickness ratio of about 5. In addition, the growth mechanism of PbS nanobelts is suggested.     

Selective effect of guest molecule length and hydrogen bonding on the supramolecular host structure

A host supramolecular structure consisting of bis-(2,2':6',2' '-terpyridine)-4'-oxyhexadecane (BT-O-C16) is shown to respond to guest molecules in dramatic ways, as observed by using scanning tunneling microscopy (STM) on a highly oriented pyrolytic graphite surface under ambient conditions. It is observed that small linear molecules can be encapsulated within the host supramolecular lattice. The characteristics of the host structure were nearly unaffected by the encapsulated guest molecules of terphthalic acid (TPA) dimers, whereas appreciable changes in cavity dimension can be observed with azobenzene-4,4'-dicarboxylic acid. The STM study and density functional theory (DFT) analysis reveal that intermolecular hydrogen bonding interaction plays an essential role in forming the assembling structures. The difference in guest molecule length is considered the important cause for the different guest-host complexes.