从文物中学化学——铁、铜性质主题式复习教学设计与实施

选择"铁、铜性质主题式复习"为案例,以铁器和铜器文物为主题背景,将铁、铜性质的复习与文物知识的介绍结合起来,使学生在学习过程中主动建构知识,在复习化学知识的同时,接触了一些文物知识,拓宽了视野,激发了学习兴趣。     

铁及其化合物教学开放性与实效性的研究

铁及其化合物是中学化学重要的元素化合物知识。新课标理念下的化学教学活动不同于传统的课堂教学。创建开放的学习环境可以激发学生学习化学的兴趣,帮助学生了解科学探究的基本过程和方法,培养学生的科学探究能力,使学生获得进一步学习和发展所需的化学基础知识和基本技能;引导学生认识化学在促进社会发展和提高人类生活质量方面的重要作用,通过化学学习培养学生的合作精神和社会责任感。开放性的教学不应该是教学表面的热热闹闹,而应该以提高教学的实效性为目的。课题组根据新的课程标准,在铁及其化合物的教学中进行了以提高教学实效性为目的的开放性教学的研究。本文叙述了本课题研究的目的、研究过程与分析、研究成果等。     

基于三重表征的实验教学——以铁的吸氧腐蚀为例

传统的铁吸氧腐蚀实验耗时长,现象不明显,课堂演示效果差。利用U型管及灵敏电流表等装置对教材中铁的吸氧腐蚀实验进行改进,并且结合原理分析完整地呈现了铁的吸氧腐蚀的宏观现象、微观本质和符号表征,丰富了学生对该部分知识的认知。研究结果表明基于三重表征的实验教学能够促进学生成绩的提高。     

基于真实情境的项目式教学在高三复习课的应用——轧钢厂废水分析处理

针对高三学生在解题和解决实际问题中缺乏对知识的整合和系统运用这一问题,围绕真实情境下的轧钢厂废水分析处理展开项目式教学。通过引导学生剖析项目任务中的化学知识和化学问题,以铁及其化合物的知识作为主线复习内容,将高中化学多个模块的知识进行结构化整合。拓宽学生认识化学问题的角度和深度,促进学生学习的热情和思维方式的转变,让化学学科核心素养得到落实。     

研究性学习中学生的学习行为分析

教学活动设计的核心问题是引导学生的学习行为,从而促进学生心理的发展。对学生的学习行为的分析可以了解学生在研究过程中对自己知识框架的构建和整合过程,以及对研究性学习目的所达到的程度。本文从学生的特征、学习风格、研究小组的分工合作、学生信息来源等方面对研究性学习中学生学习行为进行了粗略的分析。     

中学生化学学习困难的知识类型及认知分析

从化学学科知识特点来看,导致学生化学学习困难的知识包括专属知识、惰性知识、抽象知识和陌生知识4种类型。依据知识学习的信息加工理论,造成学生化学学习困难的认知因素主要包括学生的抽象概括能力不足、缺乏定量的思维方式、认知超负荷和技能尚未自动化等。     

我国2001-2013年中学化学实验学习研究热点的知识谱图

为比较准确地了解国内中学化学实验学习研究的热点和重点,为今后中学化学实验学习研究提供有力的数据与支撑,利用bicomb1.0软件与IBM SPSS20.0软件,对从中国知网中查询到的2001-2013年的518篇关于实验与化学学习的相关文献进行了知识谱图的绘制.研究结果表明,我国中学化学实验学习的研究主要涉及4大领域,分别是:高中新课程,化学实验对于化学知识的学习、素质教育,创新、观察等能力的培养等相关领域研究热点;中学化学实验对于激发学生兴趣、培养学生动手能力和课外活动作为化学教学的一种方法途径的研究热点;课堂教学中,实验教学与多媒教学等教学模式的改革、创新提升教学质量的研究热点;采用化学实验微型化、绿色化等策略来强化对学生的能力的培养.     

引导学生运用元素化合物认识模型解决实际问题的教学研究——以“菠菜补铁是真的吗”探究教学为例

针对常规元素化合物教学中的问题和学生学习的现状,设计了基于元素化合物认识模型的金属及其化合物单元复习教学。以"评估菠菜补铁是真的吗"为核心任务,突出了研究元素化合物的认识角度——化合价和物质类别;以探究实验为手段,将铁元素的定性检测和定量测定相结合,用模型拆解了一个真实、复杂的生活问题。结果表明,模型的应用有利于学生建立系统性思维,有利于学生用化学知识解决实际问题,有利于突破学生认知的障碍点,从而提高学生解决问题的能力。     

“铝及铝的化合物”教学设计

1指导思想及理论依据物质是化学学科的研究对象,元素化合物知识是化学学习的重要内容。新课程中元素化合物知识的编排较以往有了很大的改变,在必修1的阶段,主要是让学生建立以单一元素为核心的知识网络,为学生建立关于物质性质的感性认识,建立元素观、分类观和转化观等基本学科观念,为学生学习元素周期律及物质结构的相关知识奠定基础。     

生活境脉促体验 实验创新助探究—指向核心素养发展的“铁及其化合物的应用”教学实践

有机融合学生生活中的经验与体验和化学学习中的认知与思维,可优化课堂进程,提高学习效率,让化学知识建构的过程同时成为化学学科核心素养发展提升的过程。在“铁及其化合物的应用”的教学中,以“笔·墨”为情境生成真实问题,在互动、探究、体验中整合物质性质,建构思维模型,并应用模型解决问题,发展科学探究、证据推理、模型认知等化学学科核心素养。     

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.