Selective bonding of pyrazine to silicon(100)-2x1 surfaces: the role of nitrogen atoms

The covalent binding of pyrazine on Si(100) have been investigated using high-resolution electron energy loss spectroscopy (HREELS) and x-ray photoelectron spectroscopy. Experimental results clearly suggest that the attachment occurs exclusively through the bonding of the two para-nitrogen atoms with the surface without the involvement of the carbon atoms, as evidenced from the retention of the (sp2) C-H stretching mode in HREELS and a significant down shift of 1.6 eV in the binding energy of N 1s. The binding mechanism for pyrazine on Si(100) demonstrates that reaction channels for heteroatomic aromatic molecules are strongly dependent on the electronic properties of the constituent atoms.     

Highly enantioselective hydrogenation of N-phthaloyl enamides

Rh- or Ru-catalyzed highly enantioselective hydrogenation of N-phthaloyl enamides is presented. Electron-rich TangPhos and DuanPhos are found to be effective ligands for Rh-catalyzed hydrogenation of α-aryl enamides and up to 99% ee has been achieved. In contrast, for the hydrogenation of α-alkyl enamide, the Ru-C₃-TunePhos complex is more effective and up to 69% ee can be observed. This work is the first report of the hydrogenation of N-phthaloyl enamides.     

邻苯二甲酸在异丙醇-水混合溶剂中电离热力学性质的研究

The first thermodynamic dissociation constants of o-phthalic acid were determined at five temperatures from 278.15 to 318.15 K in 10, 14.93 and 20 wt% isopropanol-water solvent mixtures, by precise e. m. f. measurements of hydrogen-silver chlorld electrodes in cells without liquid junction. On the basis of Pitzer's theory, the method of polynomial approximation was used to determine the dissociation constants of H_2P and the results obtained were compared with traditional extrapolation according to the extended Debye-Huckel equation Results obtained from both methods agree within experimental error. The dependence of the first thermodynamic dissociation constant on temperature was given as a function of the thermodynamic temperature T by the empirical equation: pK_1=A_0+A_1/T+A_2/T. The thermodynamic quantities of dissociation in the mixed solvents have been calculated, and the results have been discussed.     

可逆反应的热静力学研究法

化学反应的焓变△H和平衡常数K的测定是热静力学研究的重要任务。通常用量热法可以此较准确地测定△H,但要从量热数据直接得到K则是在六十年代初才开始有所探索。在达方面,Drago和Christensen的工作是值得借鉴的。本文建立了一种中性配位体与一价金属离子络合反应体系的热静力学研究法,并用这种方法研究了二苯并18-冠-6与Na~+的络合反应,同时得到了反应的△H和平衡常数K。实验值与文献值符合。     

Simultaneously achieving high capacity storage and multilevel anti-counterfeiting using electrochromic and electrofluorochromic dual-functional AIE polymers

With the advent of the big data era, information storage and security are becoming increasingly important. However, high capacity information storage and multilevel anti-counterfeiting are typically difficult to achieve simultaneously. To address this challenge, herein, two electrochromic and electrofluorochromic dual-functional polymers with aggregation-induced emission (AIE) characteristics were rationally designed and facilely prepared. Upon applying voltages, the absorption and fluorescence spectra of the AIE polymers can undergo reversible changes, accompanied by variation of their color and emission. By utilizing the controllable characteristics of the polymers, dual-mode display devices were fabricated via a simple spraying technique. More interestingly, a four-dimensional color code device was constructed by adding color change multiplexing to the two-dimensional space, thereby achieving high capacity information storage. Moreover, the color code device can also be applied in the multilevel anti-counterfeiting area. The encrypted information can be dynamically converted under different voltages. Thus, the AIE polymers show great promise for applications in multidimensional information storage and dynamic anti-counterfeiting, and the design strategy may provide a new avenue for advanced information storage and high security technology.

By using electrical stimuli-responsive AIE polymers, dual-mode display devices, multidimensional information storage and anti-counterfeiting devices were constructed.     

Antidepressant-like effect of triterpenoids extracts from Poria cocos on the CUMS rats by 16S rRNA gene sequencing and LC–MS metabolomics

Abstract

Poria cocos is an edible medicinal mushroom with the effects of inducing diuresis, excreting dampness, invigorating the spleen and tranquilizing the mind. The triterpenoids of Poria cocos as the main active ingredients have shown health benefits of the central nervous system of the human body. Accordingly, this study aimed at further understanding the antidepressant-like effect and a potential mechanism of the triterpenoids extracts from Poria cocos (TPC). As a result, the TPC significantly ameliorated depression-like behaviors on chronic unpredictable mild stress (CUMS) rats, and restored the levels of brain-derived neurotrophic factor and nerve growth factor in the hippocampus of rats. Gut microiota analysis revealed that TPC could increase the biodiversity and markedly regulate the relative abundance of [Prevotella], Allobaculum and Ochrobactrum of CUMS rats. The cecal contents metabolomics pointed to thirteen biomarkers associated with TPC antidepressant effect, which involved in primary bile acid biosynthesis, taurine and hypotaurine metabolism, arginine and proline metabolism. Correlation analysis further showed that there was a strong correlation relationship between the gut microbiota and the cecal contents metabolites, especially compounds involved in energy metabolism, inflammation and immunity. In conclusion, TPC showed a potential antidepressant effect, which was possibly mediated the gut microbiota and cecal contents metabolism.     

氢气对氯硅烷功能化非共轭α,ω-双烯烃和丙烯共聚物链结构的影响

基于Ziegler-Natta催化剂的氯硅烷功能化非共轭α,ω-双烯烃与丙烯共聚,在水的引发下脱水缩合可有效地形成长支链结构的聚丙烯树脂.而氢气常作为丙烯聚合中的链转移剂,调控聚丙烯的分子量,基于此,研究了氢气对氯硅烷功能化非共轭α,ω-双烯烃与丙烯共聚物链结构的影响.核磁共振氢谱(~1H-NMR)测试结果表明,氢气抑制了氯硅烷功能化非共轭α,ω-双烯烃的插入,随着氢气用量的增加,共聚物分子链中端基乙烯基含量由0.12 mol%降低到0.05 mol%.熔体流变行为测试结果显示,聚合物熔体的储能模量、损耗模量和零剪切黏度均随着氢气用量增加而降低,这主要是由于相对分子质量减小和长支链密度的减少.     

Photodissociation dynamics of the methyl radical at 212.5 nm: effect of parent internal excitation

Photodissociation dynamics of the CH3 radical at 212.5 nm has been investigated using the H atom Rydberg tagging time-of-flight method with a pure CH3 radical source generated by the photolysis of CH3I at 266 nm. Time-of-flight spectra of the H atom products from the photolysis of both cold and hot methyl radicals have been measured at different photolysis polarizations. Experimental results indicate that the photodissociation of the methyl radical in its ground vibrational state at 212.5 nm excitation occurs on a very fast time scale in comparison with its rotational period, indicating the CH3 dissociation at 212.5 nm occurs on the excited 3s Rydberg state surface. Experimental evidence also shows that the photodissociation of the methyl radical in the nu2 = 1 state of the umbrella mode at 212.5 nm excitation is characteristically different from that in the ground vibrational state.     

Hydrogenation of CO over carbides of tungsten

CO hydrogenation on tungsten carbides has been investigated.The methanation activitiesof tungsten carbides are comparable to that of supported Group VIII metal catalysts.Temperature-programmed thermal desorption spectra of CO on tungsten carbide show that CO is adsorbed non-dissociatively,and the surface—CO bond appears to be rather weak.     

四川省重点河段水环境安全性评价

为研究四川省重点河段水环境的安全性,利用综合评价指数法和模糊综合评价决策的数学模型对主要水系干流和支流河段的水质安全性做出了评价.结果显示,岷江流域的水质安全性较差,主要的污染物为重金属汞和铁,沱江和涪江流域的水质安全性较好.