A Facile and Versatile Synthesis of Energetic Furazan-Functionalized 5-Nitroimino-1,2,4-Triazoles

An analogue-oriented synthetic route for the formulation of furazan-functionalized 5-nitroimino-1,2,4-triazoles has been explored. The process was found to be straightforward, high yielding, and highly efficient, and scalable. Nine compounds were synthesized and the physicochemical and energetic properties, including density, thermal stability, and sensitivity, were investigated, as well as the energetic performance (e.g., detonation velocities and detonation pressures) as evaluated by using EXPLO5 code. Among the new materials, compounds 4 – 6 and 11 possess high densities, acceptable sensitivities, and good detonation performances, and thereby demonstrate the potential applications as new secondary explosives.     

聚丙烯及增韧剂对复合材料熔接痕强度的影响

研究了聚丙烯基体的熔体粘度(以熔体流动速率表征)、增韧剂POE的粘度(以门尼粘度表征)、增韧剂POE的含量等因素对聚丙烯复合材料熔接痕强度的影响。结果表明:聚丙烯基体/增韧剂的粘度比越小,聚丙烯复合材料的熔接痕强度越高,即聚丙烯粘度越小、增韧剂粘度越大,整个复合材料的熔接痕强度越高;增韧剂POE的含量越大复合材料的熔接痕强度越小。     

Photocatalytic degradation of trichloroethylene over BiOCl under UV irradiation

In this study, BiOCl samples were synthesized under different pH values and characterized by XRD, SEM, UV‐vis DRS, BET, photoelectrochemical measurement and PL. The photocatalytic performances of the as‐prepared samples were evaluated through the decomposition of trichloroethylene (TCE) under UV irradiation. The influences of several parameters such as solution pH and common inorganic anions on TCE removal were investigated. Results indicated that BiOCl‐0.6 exhibited better photocatalytic performance than BiOCl‐6.0 because of its higher migration ability of photo‐induced carrier. The photocatalytic degradation of TCE over BiOCl‐0.6 followed pseudo first‐order kinetics and appeared to be more efficient in acidic solution than in alkaline. TCE was almost completely dechlorinated in 120 minutes. The inhibiting effect of naturally occurring anions was in the order of HCO₃^‐ >SO₄^2‐ >NO₃^‐, while Cl^‐ exhibited a dual effect. Moreover, BiOCl‐0.6 exhibited superior reusability after three cycles of repetition tests.     

A Porphyrin-Based Covalent Organic Framework for Metal-Free Photocatalytic Aerobic Oxidative Coupling of Amines

Imines are important intermediates in drug synthesis. Photocatalytic aerobic oxidative coupling of amines has been considered as a clean and promising way to produce imines and has attracted great attention. Herein, we designed and synthesized a novel two-dimensional porphyrin-based covalent organic framework (Por-BC-COF) which adopts an AA stacking mode with excellent crystallinity, high Brunauer–Emmett–Teller surface areas (1200 m² g⁻¹), wide light absorption range (200–1300 nm) and good stability in a variety of organic solvents. Por-BC-COF can be used as a metal-free heterogeneous photocatalyst for the photocatalytic oxidation of amines to imines under visible light and red light with a high yield (97 %). This work presents a novel and efficient COF photocatalyst in the application of light-driven organic synthesis.     

Global existence of solutions for a viscous Cahn–Hilliard equation with gradient dependent potentials and sources

We consider a class of nonlinear viscous Cahn–Hilliard equations with gradient dependent potentials and sources. By a Galerkin approximation scheme combined with the potential well method, we prove the global existence of weak solutions.     

Combined use of ionic liquid and β‐CD for enantioseparation of 12 pharmaceuticals using CE

In this study, the enantioseparation of zopiclone, repaglinide, chlorphenamine maleate, brompheniramine maleate, dioxopromethazine hydrochloride, promethazine hydrochloride, liarozole, carvedilol, homatropine hydrobromide, homatropine methylbromide, venlafaxine, and sibutramine hydrochloride has been investigated using β‐CD in combination with a chiral ionic liquid (IL), 1‐ethyl‐3‐methylimidazolium‐L‐lactate. The influence of the type of IL and its concentration, BGE pH, and chain length of the IL cations on the resolution are discussed. Finally, the proposed method was successfully applied for the chiral impurity determination of eszopiclone in pharmaceutical tablets after validation with respect to accuracy and precision, linearity range, selectivity, repeatability, LOD and LOQ. It is assessed that the chiral impurity determination in the commercial tables is fewer than 0.1%.     

环路跟踪卡尔曼滤波算法的性能分析

基于卡尔曼滤波的环路跟踪算法多是通过一定仿真证明算法性能,没有系统性性能评估,难以较好指导工程应用。在原有算法基础上进行了优化,并系统性地对比分析、评估了基于卡尔曼环路滤波算法性能,以期为算法工程化提供指导。首先提出对跟踪环路反馈调整量进行预测,使之更符合系统实际,减小环路跟踪误差。而后基于卫星信号模拟器输出信号和自生产信号源,充分评估基于卡尔曼滤波环路跟踪算法的收敛时间和灵敏度。仿真结果表明,相比目前工程常用的二阶FFL辅助三阶PLL算法,基于卡尔曼滤波环路跟踪算法能够缩短环路所需稳定时间约90%,并能提升跟踪灵敏度约5 d B,有效改善弱信号场景中接收机输出信息的完好性和连续性。     

海藻酸-磷脂微囊复合水凝胶的制备、表征及毒理学分析

采用薄膜分散法合成磷脂微囊,根据胶粒的双电层理论,通过在微囊中加入氯化锰、氯化钙和氯化镁电解质溶液,使微囊处于相对稳定的状态.研究发现加入氯化锰和氯化钙溶液,微囊胶体的粒径没有明显的变化,但加入一定浓度氯化镁溶液,其粒径明显变大.为了进一步增加磷脂微囊稳定性,将氯化锰、氯化钙、氯化镁磷脂微囊胶体分别与海藻酸钠(SA)溶液混合.结果表明,氯化镁与SA几乎不能形成水凝胶,氯化钙与SA形成水凝胶能力强于氯化锰.微囊胶体溶液中的磷脂酰丝氨酸(PS)可以与Ca~(2+)和Mg~(2+)键合形成PS-Ca~(2+)和PS-Mg~(2+),但不能与Mn~(2+)键合形成PS-Mn~(2+).对氯化钙磷脂微囊与海藻酸钠合成的复合水凝胶的形貌、溶胀率及细胞毒性进行了表征,结果表明,氯化钙与SA形成的水凝胶可以捕获胶体中磷脂微囊,且形貌规整,结构稳定,无细胞毒性.     

Triterpenoids with Cytotoxicity from Abelia engleriana

Chemistry of Natural Compounds -     

Novel Synthetic Approach Toward C‐Substituted Piperazine Derivatives via C‐N Bonds Formation of α‐Bromoarylethanones and Ethanolamine

A new method for the synthesis of novel C‐substituted piperazine derivatives bearing aryl substituents on 2,6‐C positions has been developed by one‐pot three‐component sequential reaction of α‐bromoarylethanones with ethanolamine in the presence of formic acid. The structure of the novel compounds was established by nuclear magnetic resonance (NMR), mass spectrometry (MS), and elemental analysis. In addition, the crystal structure of 4e was determined by single X‐ray crystallography and a possible reaction mechanism was proposed.