关于meso—四苯基卟啉在冰醋酸中的存在形式

前言卟啉在生物化学、分析化学、药物化学等领域有着广泛研究和重要应用［１～３］。近年来虽然对卟啉类化合物的研究报道很多［４～６］，但对卟啉在酸性介质中的研究很少。较早期的研究工作认为卟啉类化合物在酸性介质中仅以其二酸形式存在［７］。本文实验结果显示ｍｅ...     

Nanosized cationic and anionic manganese porphyrins as mesoporous catalysts for the oxidation of olefins: Nano versus bulk aggregates

In this study, catalytic activity of bulk and nano‐sized meso‐tetrakis(4‐sulfonatophenyl)porphyrinatomanganese(III) acetate, MnTPPS₄(OAc), (ammonium salt) and meso‐tetrakis(3‐methylpyridyl)porphyrinatomanganese(III) acetate, MnT(3‐MePy)P(OAc) (tosylate salt) for the oxidation of olefins with tetra‐n‐butylammonium Oxone has been studied and compared with that of the bulk counterparts. The nanoparticles were prepared by mixing solvent techniques using water, (triethyleneglycol) monomethyl ether and dimethylsulfoxide or acetonitrile. The formation of nano‐sized catalysts was confirmed by UV‐Vis spectroscopy, DLS and AFM. Nitrogen porosimetry measurements indicated the homogeneous pore size distribution in the bulk and nano‐sized manganese porphyrins. In spite of the high oxidizability of Oxone, the heterogenized manganese porphyrins showed a significantly higher oxidative stability relative to their homogeneous counterparts within a reaction time of 6 h. The increase in the catalytic activity induced by the formation of nano‐sized catalysts was more pronounced in the case of MnT(3‐MePy)P(OAc). MnT(3‐MePy)P(OAc) may be recovered and reused for at least 4 times without any significant decrease in the catalyst efficiency. In the case of MnTPPS₄(OAc) a large decrease in the catalytic activity was observed after the first use of the catalyst. The latter was attributed to higher degrees of catalyst degradation in the case of MnTPPS₄(OAc).     

Atropisomers of meso Tetra(N-Mesyl Pyrrol-2-yl) Porphyrins: Synthesis,Isolation and Characterization of All-Pyrrolic Porphyrins

Atropisomerism has been observed in a variety of biaryl compounds and meso-aryl substituted porphyrins. However, in porphyrins, this phenomenon had been shown only with o-substituted 6-membered aromatic groups at the meso-position. We show herein that a 5-membered heteroaromatic (N-mesyl-pyrrol-2-yl) group at the meso-position leads to atropisomerism. In addition, we report a ‘one-pot’ synthetic route for the synthesis of ‘all-pyrrolic’ porphyrin (APP) with several N-protection groups (Boc, Cbz, Ms and Ts). Among these groups, we found that only the Ms group gave four individually separable atropisomers of meso-tetra(N-Ms-pyrrol-2-yl) porphyrin. Furthermore, the reductive removal of Cbz- was achieved to obtain meso-tetra(pyrrol-2-yl) porphyrin. Thus, our synthetic procedure provides an easy access to a group of APPs and stable atropisomers, which is expected to expand the application of novel APP-based materials.     

meso-四(4-吡啶基)卟啉荧光熄灭法测定痕量钯的研究

系统地研究了在十二烷基磺酸钠（ＳＤＳ）存在下，钯（Ⅱ）与ｍｅｓｏ－四（４－吡啶基）卟啉的荧光熄灭反应．提出了高灵敏测定痕量钯（Ⅱ）的荧光分析新方法．该反应在ｐＨ值为４．６的醋酸－醋酸钠缓冲溶液中经沸水浴加热而完成，生成的配合物使卟啉的荧光强度定量熄灭，进而在强酸性条件下测量其荧光强度，发现钯（Ⅱ）的浓度在４～１２０μｇ／Ｌ范围内与显色剂的荧光强度的变化值（ΔＦ）有良好的线性关系．     

Crystalline Hetero‐Stereocomplexed Polycarbonates Produced from Amorphous Opposite Enantiomers Having Different Chemical Structures

Stereocomplexation is the stereoselective interaction between two opposite enantiomeric polymers through an interlocked orderly assembly. Most studies focus on the stereocomplex formation from the crystalline opposite enantiomers having the identical structure; nevertheless, rare examples were reported regarding the crystalline stereocomplexes from enantiomeric polymers having different chemical structures. Herein we show a strategy for polymer orderly assembly through the formation of crystalline hetero‐stereocomplexed polymeric materials by the cocrystallization of amorphous isotactic polycarbonates with different chemical structures and opposite configurations. The behaviors in the crystalline state are significantly different from that of the component enantiomeric polymers or their homo‐stereocomplexes. This study is expected to open up a new way to prepare various semicrystalline materials having a wide variety of physical properties and degradability.     

Multi-scale and multi-order singularity approach to non-equilibrium mechanics: Coupling of atomic-micro-macro damage

Offered in this work is the development of a macro/meso/micro model that covers the lineal scale of 10⁻¹¹ to 10⁰ by application of the volume energy density function. Boundary constraints and defect geometries are shown to play a role at the smaller scale in the same way as those at the macroscopic scale. Different orders of stress (or energy density) singularities are used to describe the defect geometry and prevailing constraint via the boundary conditions in a way similar to singularity adopted in classical fracture mechanics. Two classes of singularities have been identified in addition to classical one without violating the finiteness conditions of the local displacement and energy density. Still the connection of results from the different scales is no small task and is made possible by application of a scale multiplier. It is determined by considering the interactive effects of the parameters at the different scales from the atomic to the macroscopic. Unlike the classical boundary value problem approach, application of the scale multiplier has led to closed-form asymptotic multiscale solutions that otherwise would not have been made possible. The procedure is demonstrated for the anti-plane shear of a macro-micro-atomic model that accounts for imperfection at the different scales Published in Prikladnaya Mekhanika, Vol. 42, No. 1, pp. 3–22, January 2006.     

含孔隙混凝土二维细观建模方法研究

根据混凝土的细观组成和结构特点,对传统二维建模方法加以继承与改进,提出了一种高效的分步入侵判定算法.将孔隙直观地反映在模型中,建立了不同的含孔隙混凝土细观模型.对含圆形、椭圆形、多边形骨料与圆形、椭圆形孔隙的混凝土标准试件分别进行了建模研究,结果表明本文的算法具有较强适用性.同时,通过对不同面积率与多种形状骨料/孔隙混凝土的大量建模进一步验证了该算法的效率.模拟了混凝土试件在单轴压缩下的准静态力学性能,分析了混凝土内部孔隙对其裂纹扩展的主要路径、破坏模式以及宏观力学性能的显著影响.     

Tetraphenylethene-Embedded Pillar[5]arene and [15]Paracyclophane: Distorted Cavities and Host–Guest Binding Properties

Two aggregation-induced emission (AIE) macrocycles (DMP[5]-TPE and PCP[5]-TPE) were prepared by embedding Tetraphenylethene (TPE) unit into the skeletons of Dimethoxypillar[5]arene (DMP[5]) and [15]Paracyclophane ([15]PCP) at meso position, respectively. In crystal, the PCP[5]-TPE showed a distorted cavity, and the incubation of hexane inside the DMP[5]-TPE cavity caused a distinct change in the molecular conformation compared to PCP[5]-TPE. There was no complexation between PCP[5]-TPE and 1,4-dicyanobutane (DCB). UV absorption experiments showed the distorted cavity of DMP[5]-TPE hindered association with DCB.     

Easily Separated and Recyclable Amino-functionalized PorousSiO2 Beads with 3D Continuous Meso/Macropore Channels

Amino-functionalized porous SiO₂ beads with a diameter of 200—800 μm(PSB-NH₂) have been successfully synthesized by grafting 3-aminopropyl-triethoxysilane onto meso/macroporous silica beads(PSB), in which the PSB was prepared by hydrothermal synthetic method with a porous hard template anion-exchange resin. The as-prepared materials were characterized by means of nitrogen sorption and transmission electron micrographs(TEM), showing the presence of 3D interconnected and continuous large mesopores and macropores inside. The beads were used to catalyze Knoevenagel condensation and proved to be highly active and selective due to the high accessibility of the reactants to the amino groups via the continuous 3D meso/macopores. Notably, such material in bead format facilitates the extremely straightforward separation from reaction solution without any centrifugation or filtration. Moreover, PSB-NH₂ proved to be a stable catalyst via leaching experiment test, and can be easily recovered and reused without significant loss of activity in successive catalytic cycles.     

混凝土静态力学性能的细观力学方法述评

混凝土力学特性是大坝、海洋平台等工程结构抗震设计及仿真分析的前提条件之一,也是目前研究的薄弱环节. 混凝土是一种典型的非均质材料,其宏观力学特性由细观组成来决定.本文总结了目前研究混凝土宏观力学特性的细观力学分析方法,细观有限元法及理论分析法; 阐述了界面过渡区(ITZ)对混凝土性能的影响,简单介绍了混凝土界面过渡区问题的研究现状;介绍了作者提出的混凝土宏观力学性能研究的细观单元等效化分析方法.最后对其未来发展的一些方向和有待进一步研究的问题作了总结.