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221.
首次系统地推导出快中子照相像素值形成解析式, 建立图像反差不等式, 并利用该不等式首次对图像对比度与源强、照射时间和散射之间的关系进行说明. 并在像素值解析式基础上编制快中子照相模拟程序, 利用该程序对空间分辨率和图像对比度进行模拟, 并与实验对照, 研究结果表明空间分辨率模拟效果好于实验, 图像对比度模拟效果与实验相当. 最后通过对狭缝、方孔以及多材质组成的复杂样品模拟并与实验对照, 结果显示模拟效果与实验照片在反差灵敏度效果上非常一致, 该模拟计算方法可为实验设计和工程应用提供参考. 相似文献
222.
采用溶胶凝胶法与等体积浸渍相结合制备了一系列以粘土为载体的K-Co-Mo催化剂. 采用XRD、N2等温吸脱附、H26+的还原,但对Mo4+和Co2+的还原没有明显的影响. 催化剂经还原后,在其表面生成了一种更低价态的Moδ+(1<δ<4)物种,被认为是合成醇的活性中心. 与非负载催化剂相比,粘土担载的K-Co-Mo具有更高的合成醇性能. 负载型催化剂具有较高的活性物种分散度,并且其介孔结构在一定程度上延长了合成醇反应中间体的滞留时间,从而促进了低碳醇的生成. 经773 K还原的催化剂具有较高的活性,其原因可为催化剂表面具有较高含量的Moδ+物种. 相似文献
223.
Chemical depth profiling and 3D reconstruction of III–V heterostructures selectively grown on non‐planar Si substrates by MOCVD 下载免费PDF全文
V. Gorbenko M. Veillerot A. Grenier G. Audoit W. Hourani E. Martinez R. Cipro M. Martin S. David X. Bao F. Bassani T. Baron J.‐P. Barnes 《固体物理学:研究快报》2015,9(3):202-205
The chemical characterization of novel 3D architectures with nanometre‐scale dimensions is extremely challenging. The chemical composition of InGaAs/AlAs quantum wells selectively grown in SiO2 trenches, 100–300 nm wide, is studied. Combining high lateral resolution 3D ToF‐SIMS analysis and Auger measurements, the chemical composition of individual trenches was obtained confirming the uniformity of these III–V heterostructures. These results correlate well with an average approach using SIMS depth profiling. The effects of ion beam orientation on the surface topography of confined structures were highlighted. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim) 相似文献
224.
Polymers based on styrene (STY) and divinylbenzene (DVB) are widely used for water treatment. The chemical modification of these materials, with the introduction of chemical groups, increases their selectivity for certain types of contaminants. The incorporation of magnetic particles makes these systems useful for removing contaminants from aquifers, due to their magnetic attraction of certain residues. In this work, STY–DVB resins (unmodified, sulfonated, and impregnated with nickel and cobalt particles) were analyzed by thermogravimetry. The thermal stabilities of all the samples were compared, showing that sulfonation reduces the thermal stability of the resin, but the incorporation of metal particles restores that stability, with the extent of this recovery depending on the type of metal. This result shows that even when the incorporation of metal particles does not involve removal of contaminants by magnetic attraction, this inclusion is still justified because it increases the material’s thermal stability and also makes it more efficient for removing certain types of non-metallic contaminants, as observed in a previous study. Besides this, the thermogravimetric analysis was highly useful to ascertain the changes caused to the materials, including allowing inferences on the semi-quantitative results of the degree of sulfonation and confirming that metal compounds are not only physical mixtures. 相似文献
225.
Dr. Hongli Bao Liela Bayeh Prof. Uttam K. Tambar 《Angewandte Chemie (International ed. in English)》2014,53(6):1664-1668
New advances in the functionalization of unactivated olefins with carbon nucleophiles have provided more efficient and practical approaches to convert inexpensive starting materials into valuable products. Recent examples have been reported with stabilized carbon nucleophiles, tethered carbon nucleophiles, diazoesters, and trifluoromethane donors. A general method for functionalizing olefins with aromatic, aliphatic, and vinyl Grignard reagents was developed. In a one‐pot process, olefins are oxidized by a commercially available reagent to allylic electrophiles, which undergo selective copper‐catalyzed allylic alkylation with Grignard reagents. Products are formed in high yield and with high regioselectivity. This was utilized to synthesize a series of skipped dienes, a class of compounds that are prevalent in natural products and are difficult to synthesize by known allylic alkylation methods. 相似文献
226.
Photochemically Engineering the Metal–Semiconductor Interface for Room‐Temperature Transfer Hydrogenation of Nitroarenes with Formic Acid 下载免费PDF全文
Dr. Xin‐Hao Li Yi‐Yu Cai Ling‐Hong Gong Dr. Wei Fu Dr. Kai‐Xue Wang Dr. Hong‐Liang Bao Dr. Xiao Wei Dr. Jie‐Sheng Chen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(50):16732-16737
A mild photochemical approach was applied to construct highly coupled metal–semiconductor dyads, which were found to efficiently facilitate the hydrogenation of nitrobenzene. Aniline was produced in excellent yield (>99 %, TOF: 1183) using formic acid as hydrogen source and water as solvent at room temperature. This general and green catalytic process is applicable to a wide range of nitroarenes without the involvement of high‐pressure gases or sacrificial additives. 相似文献
227.
Tailoring 3,3′‐Dihydroxyisorenieratene to Hydroxystilbene: Finding a Resveratrol Analogue with Increased Antiproliferation Activity and Cell Selectivity 下载免费PDF全文
Yan‐Fei Kang Wen‐Jing Yan Ting‐Wen Zhou Dr. Fang Dai Dr. Xiu‐Zhuang Li Xia‐Zhen Bao Yu‐Ting Du Cui‐Hong Yuan Hai‐Bo Wang Xiao‐Rong Ren Dr. Qiang Liu Dr. Xiao‐Ling Jin Prof. Dr. Bo Zhou Prof. Dr. Jie Zhang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(29):8904-8908
Four novel compounds were designed by “tailoring” 3,3′‐dihydroxyisorenieratene (a natural carotenoid) based on an isoprene unit retention truncation strategy. Among them, the smallest molecule 1 (2,3,6,2′,3′,6′‐hexamethyl‐4,4′‐dihydroxy‐trans‐stilbene) was concisely synthesized in a one‐pot Stille–Heck tandem sequence, and surfaced as a promising lead molecule in terms of its selective antiproliferative activity mediated by blocking the NCI‐H460 cell cycle in G1 phase. Additionally, theoretical calculations and cell uptake experiments indicate that the unique polymethylation pattern of compound 1 significantly induces a conformational change shift out of planarity and increases its cell uptake and metabolic stability. The observation should be helpful to rationally design resveratrol‐inspired antiproliferative agents. 相似文献
228.
Dr. Hoon Hyun Dr. Hideyuki Wada Dr. Kai Bao Dr. Julien Gravier Dr. Yogesh Yadav Dr. Matt Laramie Dr. Maged Henary Dr. John V. Frangioni Dr. Hak Soo Choi 《Angewandte Chemie (International ed. in English)》2014,53(40):10668-10672
The conventional method for creating targeted contrast agents is to conjugate separate targeting and fluorophore domains. A new strategy is based on the incorporation of targeting moieties into the non‐delocalized structure of pentamethine and heptamethine indocyanines. Using the known affinity of phosphonates for bone minerals in a model system, two families of bifunctional molecules that target bone without requiring a traditional bisphosphonate are synthesized. With peak fluorescence emissions at approximately 700 or 800 nm, these molecules can be used for fluorescence‐assisted resection and exploration (FLARE) dual‐channel imaging. Longitudinal FLARE studies in mice demonstrate that phosphonated near‐infrared fluorophores remain stable in bone for over five weeks, and histological analysis confirms their incorporation into the bone matrix. Taken together, a new strategy for creating ultra‐compact, targeted near‐infrared fluorophores for various bioimaging applications is described. 相似文献
229.
Porous CuO micro‐/nanostructures with clean surface, prepared through Cu2(OH)2CO3 precursor followed by calcination in air, were proven to be an effective peroxidase mimic. They can quickly catalyze oxidation of the peroxidase substrate 3,3′,5,5′‐tetramethylbenzidine (TMB) in the presence of H2O2, producing a blue color. The obtained porous CuO micro‐/nanostructure have potential application in wastewater treatment. The apparent steady‐state kinetic parameter was studied with TMB as the substrate. In addition, the potential application of the porous CuO in wastewater treatment was demonstrated with phenol‐containing water as an example. Such investigation not only confirms the intrinsic peroxidase‐like activity of micro‐/nanostructured CuO, but also suggests its potential application in wastewater treatment. 相似文献
230.
哈茨木霉CGMCC 2979生物转化栀子中的京尼平苷制备京尼平 总被引:1,自引:0,他引:1
采用微生物直接转化药材的方法,将栀子中的京尼平苷转化为京尼平,无需糖苷酶和京尼平苷的制备. 在培养温度为30 ℃,pH 6.1以及栀子载量为80 g/L的条件下,48 h京尼平苷的转化率为97.8%. 转化后的京尼平通过XAD-16N大孔树脂偶联硅胶层析的方法,制备得到纯度大于95%的京尼平,收率为62.3%. 在催化、转化机制研究中,从哈茨木霉CGMCC2979的发酵液中分离得到了分子量为74.4 kDa的京尼平苷β-葡萄糖苷酶,该酶最优催化条件为50 ℃和pH 4.0-5.0. Km和Vmax分别为3.6 mmol/L和775 μmol/h/mg蛋白. 本文提供了一种简便、高效制备京尼平的新方法. 相似文献