高中化学教师无机元素化合物知识的调查研究

选取吉林省长春市及其周边地区部分高中化学教师为样本,以问卷方式测查了教师无机元素化合物知识的掌握情况。发现教师对于高中化学体系中的无机元素化合物知识掌握得较好,但是不能很好地从化学学科层面去分析和理解教学中的问题;教龄、职称、教过毕业班次数、学校所在地和学校类型5个因素对教师学科知识的掌握情况有显著的影响。     

逆向设计在素养导向的单元教学设计中的应用——以“钠及其化合物”单元为例

逆向教学设计被称为“通过设计促进理解”的教学设计。教学过程中,教师结合课程标准相关要求进行单元逆向教学设计,有助于学生提升学科核心素养,引发深度学习。围绕“钠及其化合物”开展了逆向设计的相关探索。根据逆向设计模板,同时,结合本单元学生需要获取的目标、知识和表现性任务,设计了4个课时的教学任务。单元教学过程整体实现了初始培养学生从微观结构出发,结合实验事实认识钠的性质,进而到学生分析物质性质的相似性和差异性,然后到学生结合相关资料实现鉴别实验方案的设计,最终学生结合相关资料进行纯碱制备工业应用。通过总结学生在“钠及其化合物”单元教学各环节中的表现情况,包括课堂实录、完成表现性任务、以及针对授课学生、同行专家的调研问卷情况,整理了“钠及其化合物”单元教学过程中的相关收获以及反思。相关单元设计的认识可为今后落实“素养为本”的教学提供一定的参考。     

“铜元素化合物”的高三线上主题式复习*

以高三复习课“铜元素化合物”的教学为例,基于主题教学思想,从“价类二维图”出发,引导学生从物质类别、氧化还原和化学平衡等多角度认识元素化合物间的相互转化,实现了主题内容的关联与进阶,促进了学生思维能力的提升和学科观念的建构。本节课是网络直播课,采用“腾讯课堂”平台,学生可以连麦回答问题,学生设计的实验方案发布在班级微信上,由教师共享屏幕,则所有学生可见。     

不同发展阶段高中化学教师的PCK表征研究*——以“物质的量”主题为例

为探讨不同发展阶段的高中化学教师对于“物质的量”主题的认识,聚焦学科教学知识(PCK)的2个基本组成部分:(1)学生理解的知识,(2)教学策略和表征知识。基于PCK课堂观察量表和CoRe模型,对比分析新手、熟手、专家型教师关于“物质的量”主题的PCK表征。研究结果表明,不同发展阶段化学教师的PCK存在差异,教师对学生知识的理解影响了教学策略和表征方式的决策。     

新课程下高中元素化合物知识体系的构建

在分析高中新课程对元素化合物知识的安排及其在新课程体系中地位的基础上,探讨了新课程下高中元素化合物知识的教学策略。在必修教学中通过多种途径促进学生获得有关物质及性质的事实;在选修教学中采用“先行组织者”策略将元素化合物知识融入学科知识体系。     

元素化合物知识在不同阶段层级发展的实践研究

高中化学新教材在内容的编排上体现了“螺旋式”上升的特点,教学中如何体现这个特点？需要教师整体把握同一内容在不断阶段的层级发展,分层落实知识。本文提出了高中学习元素化合物知识的4个阶段,每个阶段的知识和认识的层级是不同的,并结合氨气的教学实例进行了阐述。     

试论元素化合物教学中的几种关系

元素化合物知识在中学化学教材中占有重要地位。调查了解发现,有部分中学化学教师对元素化合物知识的重要性认识不足,认为元素化合物知识内容多、头绪多,仅是描述性教材,学生自己能看懂,没有什么好讲的;用不着认真钻研教材和大纲,用不着仔细考虑教学方法。并认为元素化合物知识远不及化学概念、化学理论、化学计算讲起来生动活泼。     

无机化学元素化合物教学中的兴趣培养

针对无机化学元素化合物知识多而杂、难以掌握的特点,沿教学过程的顺序从5个方面探讨了如何激发、培养、强化、增添、发展学生学习兴趣,以期改善元素化合物知识的教学状况,使学生在愉快的氛围中掌握繁琐的知识。     

基于学生核心素养培养的教学活动设计研究——以“氯的单质及化合物”单元教学为例

以“氯的单质及化合物”单元教学为例,研究了旨在培养学生核心素养的教学活动设计,提出了教学活动设计的一般原则、教学活动的一般类型,总结了教学活动设计的灵感来源。通过一系列连续的教学活动,提升了学生教学过程的参与度和学习效率,调动了学生学习和创新的积极性,培养了核心素养。     

化学教学设计能力评价量表的编制与应用研究

基于学科教学知识（PCK）编制化学教学设计能力评价量表，并对在职高中化学教师的教学设计能力进行评价，分析化学教师在教学设计中存在的问题，为提高在职高中化学教师教学设计能力提供有针对性的建议。研究表明：（1）高中化学教师在课程知识、学生知识及评价知识维度的项目上均处于未掌握等级；（2）高中化学教师在教学目标知识和教学策略知识维度的多个评价项目上处于基本掌握等级。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.     

A general and convenient synthesis of 4-(tosylmethyl)semicarbazones and their use in amidoalkylation of hydrogen,heteroatom, and carbon nucleophiles

A general synthesis of previously unknown semicarbazone-based α-amidoalkylating reagents, 4-(tosylmethyl)semicarbazones, has been developed. The synthesis involved three-component condensation of semicarbazones of aliphatic or aromatic aldehydes with the same or other aldehydes and p-toluenesulfinic acid. The scope and limitations of this reaction were investigated. The compounds obtained were demonstrated to be an efficient α-(4-semicarbazono)alkylating agents. They were reacted with H- (sodium borohydride), O- (sodium methylate), S- (sodium phenylthiolate), N- (pyrrolidine, sodium succinimide), P- (trialkyl phosphites), and C-nucleophiles (sodium diethyl malonate) to give the corresponding products of the tosyl group substitution, 4-substituted semicarbazones, including analogues of nitrofurazone. Among the prepared compounds tested in vitro for antibacterial and antifungal activity, three nitrofuryl-containing semicarbazones exhibited high biological activities with minimum inhibitory concentration (MIC) values of 8–32 μg/mL.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

Regiospecific and direct imidation of the methyl C(sp³)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.     

Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde

A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki–Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.