1,3‐dipolar cycloaddition reactions of nitrile oxides to prop‐1‐ene‐1,3‐sultone

The reaction of prop‐1‐ene‐1,3‐sultone 1 with a variety of nitrile oxides 3 afforded novel [3+2] cycloaddition products 4 in good yield. The cycloaddition reaction achieved excellent regioselectivity.     

超大规模集成电路波导光互连技术的现状与前景

介绍超大规模集成电路(VLSI)波导(?)互连技术的最新进展,并预测其发展方向,以及如阿解决存在的实际问题。     

磁共振现代射频脉冲理论在非均匀场成像中的应用

在磁共振非均匀场成像中，传统的射频脉冲导致回波信号的衰减.为了减小和消除这种磁共振信号的衰减，在讨论了经典理论的基础上根据非线性动力学中的逆散射理论和Shinnar-Le Roux方法导出了用于非均匀场成像的射频脉冲设计方法.模拟结果表明，采用逆散射理论和Shinnar-Le Roux方法优化的脉冲序列可以明显提高信号的信噪比. 关键词： 磁共振成像 射频脉冲 非线性系统     

Process optimization studies of 10-Hydroxycamptothecin (HCPT)-loaded folate-conjugated chitosan nanoparticles by SAS-ionic crosslink combination using response surface methodology (RSM)

10-Hydroxycamptothecin (HCPT) is a well-established topoisomerase I inhibitor of a broad spectrum of cancers. However, poor aqueous solubility, low instability, and toxicity to normal tissues have limited its clinical development. A novel HCPT-containing drug carrier system was developed to overcome these disadvantages. The response surface methodology was used to optimize the process of preparing HCPT-chitosan nanoparticles (HCPT-CSNPs) by the SAS-ionic crosslink (supercritical antisolvent SAS) combination method; the resulting HCPT-CSNPs were then conjugated with folate for specific targeting. A central composite design, composed of four independent variables, namely, chitosan concentration, TPP concentration, HCPT nanoparticle concentration, and crosslink time, was applied in the modeling process. The mean particle size and drug entrapment efficiency (DEE) of HCPT-CSNPs were chosen as response variables. The interactive effects of the four independent variables on the response variables were also studied. Nanoparticle characteristics such as morphology, DEE, and mean particle size were investigated. The optimum conditions for preparing HCPT-CSNPs were determined as follows: folate-coupled chitosan concentration 2.46 mg/ml, TPP concentration 7.73 mg/ml, HCPT nanoparticle concentration 0.48 mg/ml, and crosslinking time 47.4 min. Optimum conditions for preparing desired HCPT-CSNPs with a mean particle size of 173.5 nm and entrapment efficiency of 77.3% were obtained. The resulting folate-conjugated HCPT-CSNPs (FA-HCPT-CSNPs) reveal that the amount of folate conjugation was 197.64 mg/g CS. FA-HCPT-CSNPs used in drug carrier systems could have potential value in HCPT-sensitive tumors.     

以学生为中心的物理化学远程教学初探

在抗击新冠疫情期间,北京师范大学"物理化学"教学团队综合利用中国大学MOOC、雨课堂、微信群等多个网络平台和工具,探索并实践了以MOOC授课为基础、以学生学习为中心、以教师辅导为支撑的物理化学远程教学。我们以难度最大的"统计热力学基础"教学为例,设计了包括课前预习、课上观看MOOC视频、实时在线练习、教师答疑、课后反思提问等多环节的复合式教学方案,引导学生利用教师预留的资料、设计的教学活动以及布置的线上作业等实施自主学习。实践表明,这个多环节的综合设计在线课程能够充分调动学生的学习热情,培养学生的自我管理能力,锻炼学生的批判性思维,取得了良好的教学效果。     

Covalent Assembly of MoS2 Nanosheets with SnS Nanodots as Linkages for Lithium/Sodium‐Ion Batteries

Weak van der Waals interactions between interlayers of two‐dimensional layered materials result in disabled across‐interlayer electron transfer and poor layered structural stability, seriously deteriorating their performance in energy applications. Herein, we propose a novel covalent assembly strategy for MoS₂ nanosheets to realize unique MoS₂/SnS hollow superassemblies (HSs) by using SnS nanodots as covalent linkages. The covalent assembly based on all‐inorganic and carbon‐free concept enables effective across‐interlayer electron transfer, facilitated ion diffusion kinetics, and outstanding mechanical stability, which are evidenced by experimental characterization, DFT calculations, and mechanical simulations. Consequently, the MoS₂/SnS HSs exhibit superb rate performance and long cycling stability in lithium‐ion batteries, representing the best comprehensive performance in carbon‐free MoS₂‐based anodes to date. Moreover, the MoS₂/SnS HSs also show excellent sodium storage performance in sodium‐ion batteries.     

Spatially Controllable DNA Condensation by a Water‐Soluble Supramolecular Hybrid of Single‐Walled Carbon Nanotubes and β‐Cyclodextrin‐Tethered Ruthenium Complexes

A supramolecular hybrid is prepared by the supramolecular surface modification of single‐walled carbon nanotube (SWCNT) with cationic β‐cyclodextrin‐tethered ruthenium complexes through a spacer molecule that contains both an adamantane and a pyrene moiety. By employing the supramolecular hybrid, spatially controllable DNA condensation along the SWCNT skeleton is achieved by anchoring cationic ruthenium complexes on the surface. Furthermore, because of the unique physiological properties of SWCNTs, the cationic supramolecular hybrid can be used as a nonviral gene delivery system with the ruthenium complexes as a fluorescent probe to monitor uptake of DNA by cells.     

大气丙酮碳同位素组成测定方法的研究

利用气相色谱/燃烧/同位素比值质谱(GC/C/IRMS)分析技术,研究了具有不同碳同位素组成的丙酮与衍生剂2,4-二硝基苯肼(DNPH)的液相反应及其相应的气相反应实验过程中的碳同位素效应,探讨了以该方法测定大气丙酮碳同位素组成的可行性。研究结果表明,在衍生化过程中不会产生碳同位素分馏。本实验通过测定衍生剂DNPH与相应的衍生物的碳同位素值,大气中丙酮碳同位素组成通过质量平衡方程计算而求得。采用该方法对大气丙酮碳同位素组成的初步测定结果表明,具有相同排放源的大气丙酮碳同位素比值基本不变。本方法实验重现性好,测定精度高,可以用于分析大气丙酮的排放源研究。     

纳秒激光诱导C60分子碎裂中轻碎片离子C+n(n《30)的产生机理研究

采用飞行时间质谱计测量了纳秒激光诱导C60分子碎裂中轻碎片离子C n(n≤11)的初始平均动能,结果显示轻碎片离子具有相同的初始平均动能(约为0.34 eV),并且该动能在一定范围内不随激光通量的变化而明显改变.结合前人的实验结果,对纳秒激光诱导C60分子碎裂中轻碎片离子C n(n<30)的主要产生模式作了新的阐述,即C60分子级联发射15个C2分子和一个电子形成自身不稳定的C 30离子,在皮秒时间尺度内C 30离子的笼形结构塌陷,进而轻碎片离子产生.     

A three‐dimensional coordination polymer based on the Zn4(μ3‐OH)2 unit: poly[[(μ4‐benzene‐1,4‐dicarboxylato)bis(μ3‐benzene‐1,4‐dicarboxylato)bis(μ3‐hydroxido)bis(1,10‐phenanthroline‐5,6‐dione)tetrazinc] dihydrate]

The title compound, {[Zn₄(C₈H₄O₄)₃(OH)₂(C₁₂H₆N₂O₂)₂]·2H₂O}_n, has been prepared hydrothermally by the reaction of Zn(NO₃)₂·6H₂O with benzene‐1,4‐dicarboxylic acid (H₂bdc) and 1,10‐phenanthroline‐5,6‐dione (pdon) in H₂O. In the crystal structure, a tetranuclear Zn₄(OH)₂ fragment is located on a crystallographic inversion centre which relates two subunits, each containing a [ZnN₂O₄] octahedron and a [ZnO₄] tetrahedron bridged by a μ₃‐OH group. The pdon ligand chelates to zinc through its two N atoms to form part of the [ZnN₂O₄] octahedron. The two crystallographically independent bdc²⁻ ligands are fully deprotonated and adopt μ₃‐κO:κO′:κO′′ and μ₄‐κO:κO′:κO′′:κO′′′ coordination modes, bridging three or four Zn^II cations, respectively, from two Zn₄(OH)₂ units. The Zn₄(OH)₂ fragment connects six neighbouring tetranuclear units through four μ₃‐bdc²⁻ and two μ₄‐bdc²⁻ ligands, forming a three‐dimensional framework with uninodal 6‐connected α‐Po topology, in which the tetranuclear Zn₄(OH)₂ units are considered as 6‐connected nodes and the bdc²⁻ ligands act as linkers. The uncoordinated water molecules are located on opposite sides of the Zn₄(OH)₂ unit and are connected to it through hydrogen‐bonding interactions involving hydroxide and carboxylate groups. The structure is further stabilized by extensive π–π interactions between the pdon and μ₄‐bdc²⁻ ligands.