以化学学科关键能力为导向的化学实验探究试题的命制——以“硫化钠长期放置氧化产物检验的实验”为例

基于文献研究和真实实验探究,以“硫化钠长期放置氧化产物检验的实验”为素材命制高三实验探究试题,展示命制过程,阐释以化学学科关键能力为导向的化学实验探究试题的命制策略。     

以科学探究素养为导向的化学实验探究试题的命制——以氯化铁与硫化钠的反应现象为例

针对相关文献中的矛盾与不足之处,进一步实验探究了FeCl3滴定Na2S的反应现象,并以此为素材命制了高三实验探究试题,阐述了以科学探究素养为导向的试题命制策略。     

以科技论文为素材的高中化学试题命制策略

命制模拟试题时,教师一般会选择化学科技论文作为试题的背景材料。通过分析近3年江苏高考化学试题,可以看出流程图题考查的基本情况。以江苏某市高考模拟化学卷为例,从4个维度阐述了以科技论文为素材的高中化学试题的命制策略：选择合适的命题背景素材;将文字内容巧妙地转化为工艺流程图;建立背景素材与试题考查之间的联系;精心设计试题设问。根据命题实践提出命制试题的关注点。     

以模型认知素养为导向的电化学模拟题的命制*——以双极膜的应用为例

以双极膜发展进程为线索,以海水淡化、钠碱循环法脱除烟气中的SO₂等现实发展中真实问题为载体,结合中学生的认知能力水平,构建了电化学双极膜认识模型;命制了双极膜及其应用的电化学模拟题,以此测查学生模型认知素养的水平等级。阐述命题策略及过程,提供以模型认知素养为导向的试题命制思路;从模型建构的角度对2020年高考新课标Ⅰ卷第12题进行了评析。     

以“光发动机”为素材的习题命制的探究

针对一道有关"光发动机"的习题解答问题,通过文献研究了光发动机的工作原理和NO2的相关性质,提出了习题的修改意见和对习题命制的思考。     

基于“真实情境与实际问题”的化学试题命制——以“碳九泄漏事故”为例

以“11·4福建泉港碳九泄漏事故”为测试载体,在深入挖掘和甄选考点后,结合当前《普通高中化学课程标准（2017年版）》对考试评价的有关说明和试题命制基本理论及技术要求,命制了一道高中化学考试试题,并在文中对试题的测试目标,如认知操作、核心素养和达到的学业质量水平加以详细分析,对试题命制的技术性要求辅以论证,以期能给同行以核心素养为测试宗旨的命题提供一些参考。     

以水煤气为原料的合成

证明了在常墨及中堡下用沉搬截铜催化倒(I)巡行合成峙,原料水煤氧中硫含量可以此文献上韶载的增加很多倍而(I)不致中毒.在常赓下,有楼硫(CS:和C 05)含量(H)篇朋毫克/米,,合成温度225",空简流速需80,雨涸月的妻命备t麟中(I)业未赞生中毒现象.(l)活性瞥一度下降是因真表面上覆盖了一屠嫩,担油洗俊,活性立刻恢徨和新解     

以延伸课堂实验与发展化学学科能力为导向的期末试题的命制——学生必做实验“简单配合物的制备”

通过实验探究和文献研究,以学生必做实验“简单配合物的制备”为素材命制高二化学期末实验探究题,展现命题过程。阐释了以延伸课堂实验与发展化学学科能力为导向的期末试题命制策略。     

以硅酸盐材料为背景的教学素材开发

针对一线教师在设计硅酸盐材料一课时面对的困难,开发了与陶瓷、玻璃、水泥相对应的石家河红陶杯、洛阳浮法玻璃、白鹤滩大坝等3个教学素材。包含2个原创实验、7个资料、14个原创提问。开发的素材可用于硅酸盐材料高一新授课或以硅酸盐材料为情境的高三复习课中,也可为原创题的命制者提供参考。素材的选择遵循了立德树人的理念,培养了学生的爱国情怀,同时也提升了高级思维能力。     

基于学科思想方法的命题与教学反思——以初中学业考试化学试题为例

基于化学思想方法的命题,应以核心知识为载体,设置真实问题情境,聚焦核心素养,考查核心能力。针对化学学科思想,将其嵌入典型试题的命制中,从能力立意的命题视角,构建问题解决的思维模型。基于考后数据的统计和分析,评价学科思想方法在教学中的落实情况,诊断教学效果,并在此基础上提出教学反思。     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

Synthesis of pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles by Curtius reaction in Morita-Baylis-Hillman derivatives

Synthesis of substituted pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles from the Morita-Baylis-Hillman derivatives of acrylates via saponification followed by Curtius reaction is described.     

正丁胺对激光染料荧光谱影响的研究

用正丁胺作为碳源,采用射频辉光放电制备碳膜,选用激光染料R6G和聚乙二醇混合液作为蒸气源,采用单源热蒸发,在蒸发室与染料同时沉积得到混合膜,用拉曼光谱和红外光谱分析了碳膜的结构和键合方式,分析表明:碳膜中存在胺基团和氢原子.混合膜的荧光谱测量结果表明,认为正丁胺对染料荧光谱的影响是因为胺基和氢原子的存在.     

Cu0-catalysed 1,3-dipolar cycloadditions of α-amino acid derived N,N-cyclic azomethine imines to ynones

A series of 20 CuAIAC reactions between eight 4-acylamino substituted pyrazolidine-3-one-1-azomethine imines and four terminal ynones were performed using Cu⁰ as catalyst. The corresponding fluorescent cycloadducts were obtained in very high yields upon simple workup. Thus, Cu-metal turned out to be a better catalyst than Cu^I in terms of yield and ease of isolation. Availability of azomethine imines, mild reaction conditions, and simple workup enable a “click” access to libraries of densely substituted 2,3-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-ones. Reactivity of differently substituted dipoles was evaluated experimentally and by quantum chemical methods (DFT).     

Synthesis and antioxidative/anti-inflammatory activity of novel fullerene–polyamine conjugates

(E)-4-(Fullerenopyrrolidin-1-yl)-3-methylbut-2-enoic acid and its corresponding succinimidyl ester, readily obtained through Prato-type modification of C₆₀, were used for the selective N-acylation of polyamines. The thus obtained conjugates were evaluated for their antioxidative and anti-inflammatory activity and their cytotoxicity was determined. Members of this family of compounds showed interesting anti-lipid peroxidation, anti-lipoxygenase and anti-inflammatory activity and comparable cytocompatibility to spermidine.