Metal-free cascade boron-heteroatom addition and alkylation with diazo compounds

Transition metal-catalyzed carbene transfer reaction is one of the most notable advances for C-C bond formation reactionsduring the past decade,which has been widely employed in the preparation of C3-substituted indoles,Here,we described an efficient exa mple of catalyst-and metal-free aminobo ration of alkynes and C—C bond formation with diazo compounds to produce C3-substituted indoles,Diverse alkynyla nilines and diazo compounds ca n be utilized for this tandem transfo rmation under mild reaction conditions,re sulting in broad functional group co mpatibility.Additionally,this metal-free strategy can be extended to construct substituted benzofurans.     

低温预冷换热规律及表面改性影响研究

调研了低温管路预冷及两相换热的研究现状,阐述了低温预冷瞬态换热特性;介绍了金属表面改性对预冷规律的影响,仿真了低导热涂层管的预冷换热规律.研究发现:液氮预冷主要由膜态沸腾支配,且预冷耗时较长;液氢预冷未见膜态沸腾,预冷耗时更短.促进膜态沸腾向过渡沸腾的更早转化有利于预冷加速,且转化温度迁移可通过内壁表面结构改性实现,可...     

The Carboxyl Functionalized UiO-66-(COOH)2 for Selective Adsorption of Sr2+

Efficient and selective removal of ⁹⁰Sr is an important process for the safe use of nuclear energy. Herein, we investigate and assess the Sr²⁺ adsorption properties of a metal-organic framework UiO-66-(COOH)₂ functionalized by non-bonded carboxylic groups. This MOF is an exciting class of free carboxylic functionalized MOFs that combine chemical stability with gas sorption, dye elimination, and conductivity. Specifically, we show that uniformly distributed carboxyl and water stability make it accessible for loading Sr²⁺ without structural changes. The FTIR spectroscopy, PXRD analysis, XPS, and SEM-EDS studies show excellent stability as well as the strong affinity between -COOH active site and Sr²⁺. This strong coordination interaction guarantees a high adsorption capacity of 114 mg g⁻¹ within 5 h (pH 5 and 298 K). Combined kinetic and thermodynamic studies show that the surface complexation is strong chemisorption and cost-effective spontaneous process (ΔG = −5.49 kJ mol⁻¹~−2.16 kJ mol⁻¹). The fact that UiO-66-(COOH)₂ not only possesses a high adsorption capacity, but also enables selectivity to Sr²⁺ in the presence of similar radius ions Na⁺ and K⁺, prefigures its great potential for the practical treatment of radioactive Sr²⁺ in polluted water.     

具有全色发光的非芳香聚马来酰亚胺

<正>有机发光材料由于分子结构多样、发光颜色可调、加工简便等优点受到广泛关注。经典有机发光分子往往含有大的π共轭结构,并由此产生充分的电子离域。然而,此类有机发光分子往往含有稠环或芳杂环结构,具有潜在的细胞毒性^[1];且在调节发光颜色时往往需要增加分子共轭、改变取代基或引入不同的推拉电子结构,合成步骤较为繁琐。与之相比,不含大型共轭单元而仅含N、O、S、P等杂原子及C=O、C=N、C≡N、C=C等富电子单元的非典型发光化合物结构简单,可通过商购或简单反应获得。且许多非典型发光分子与生物体系密切相关,生物相容性良好,有利于后续应用^[2]。     

Single-Step Hydrothermal Synthesis of Biochar from H3PO4-Activated Lettuce Waste for Efficient Adsorption of Cd(II) in Aqueous Solution

Developing an ideal and cheap adsorbent for adsorbing heavy metals from aqueous solution has been urgently need. In this study, a novel, effective and low-cost method was developed to prepare the biochar from lettuce waste with H₃PO₄ as an acidic activation agent at a low-temperature (circa 200 °C) hydrothermal carbonization process. A batch adsorption experiment demonstrated that the biochar reaches the adsorption equilibrium within 30 min, and the optimal adsorption capacity of Cd(II) is 195.8 mg∙g⁻¹ at solution pH 6.0, which is significantly improved from circa 20.5 mg∙g⁻¹ of the original biochar without activator. The fitting results of the prepared biochar adsorption data conform to the pseudo-second-order kinetic model (PSO) and the Sips isotherm model, and the Cd(II) adsorption is a spontaneous and exothermic process. The hypothetical adsorption mechanism is mainly composed of ion exchange, electrostatic attraction, and surface complexation. This work offers a novel and low-temperature strategy to produce cheap and promising carbon-based adsorbents from organic vegetation wastes for removing heavy metals in aquatic environment efficiently.     

Unraveling the condensation reactions of heterometallic {BiNb_4} moieties into hybrid Bi_xNb_y-oxo clusters with mass spectrometry

The most effective methodologies for the construction of polynuclear complexes usually take advantage of preorganized building blocks.Herein,we successfully developed a new versatile heterometallic{BiNb₄}moiety,which can be applied for the assembly of less explored organic-inorganic hybrid polyoxoniobates.Through controlled condensation reactions,three{BiNb₄}moieties can be assembled into a pair of isomeric Bi₃Nb₁₈clusters at different temperatures;whilst four{BiNb₄}moieties can be combined into two unique Bi₄Nb₁₆and Bi₄Nb₁₈tetramers in different solvents.Interestingly,we have used mass spectrometry to probe the above condensation reactions,which clearly confirmed a stepwise bottom-up assembly process by capturing the presence of bismuth subsalicylate precursors,salicylate coordinated intermediates,Nb incorporated{BiNb₄}moieties and the final Bi_xNb_y-oxo clusters,respectively.Moreover,the packing modes of the{BiNb₄}units induce different solution behaviors,and the{BiNb₄}units in Bi4Nb16can be recombined by post-synthetic recrystallization in acetonitrile to produce a new tetramer Bi₄Nb₁₈-R.Therefore,this work provides not only a useful{BiNb₄}building unit but also the mechanism for their condensation,both of which will promote the future development of metal-oxo clusters.     

双涂层光纤应变传感器的理论与实验研究

对带有聚合物涂敷层和缓冲层的光纤应变传感器的力学特性进行了研究,建立了双涂层光纤与基体材料相互作用的线弹性理论模型.理论研究表明：在小半径近似条件下,双涂层光纤的力学传递特性决定于涂覆层和缓冲层的弹性模量的相对值;当缓冲层的弹性模量远大于涂覆层时,其作用可忽略.实验中,将光纤传感器埋入基体材料内部,利用白光干涉应变测量方法,对平均应变传递系数进行了实验研究.实验结果与理论仿真具有较好的一致性.     

交叉相位调制对非线性光纤环镜中光脉冲传输的影响

基于耦合非线性薛定谔方程,采用分步傅里叶方法分析了在单波长信道和WDM（波分复用）4波长信道中XPM（交叉相位调制）对高速NOLM（非线性光纤环镜）光开关中脉冲传输的影响.数值计算表明：XPM造成NOLM中信号脉冲串扰与畸变,并造成NOLM开关性能的下降.WDM系统NOLM光纤环中的同向传播的各波长之间的XPM串扰比相向脉冲之间的XPM效应的影响更大,并且波长越短输出功率越低,中间信道受XPM的影响所导致的脉座现象和走离效应比两侧波长信道严重.     

偏振模色散对非线性光纤环镜微波光子开关的影响及其补偿

建立了考虑PMD在内的NOLM微波光子开关光波传输方程,给出了基于耦合非线性薛定谔方程的分步傅里叶法,三维庞加莱球理论和琼斯传输矩阵法的数值分析模型.仿真获得在光子开关中微波直接强度调制光载波的传输过程,以及在不同调制带宽下一阶和二阶PMD对光波信号和NOLM功率传输函数的影响.指出PMD造成NOLM开关性能钝化和消光比严重恶化,并引起信号信噪比下降和旁瓣泄漏.当调制带宽大于40GHz时,二阶PMD的影响比一阶PMD更加严重.最后讨论了NOLM中的PMD补偿问题.     

荧光光纤光栅传感特性的实验研究

在载氢掺铒光纤上写入Bragg光纤光栅,得到新型光子学器件-荧光光纤光栅.分别对其Bragg波长（λB）及荧光寿命（τ）的温度（T）及应变（ε）响应特性进行了实验研究,并且给出了λB和τ分别关于（T,ε）的拟合方程.实验结果表明：荧光光纤光栅的λB对T和ε的响应具备一般Bragg光纤光栅的优良特性,测得温度灵敏度为11.1pm /℃,应变灵敏度为1.19pm/με;而且τ对T和ε的响应也具有良好的线性关系,温度灵敏度为0.59 μs/℃,应变灵敏度为6.16 ns/με.实验结论为解决温度应力交叉敏感、实现温度应力的同时监测提供一条新颖的途径.