高中化学新手熟手教师学科教学知识对比研究*

以“化学平衡”教学主题为载体自编调查问卷,选取河北省79位在职高中化学新手教师和81位高中化学熟手教师进行学科教学知识测查。应用独立样本t检验对调研数据进行比较和分析,重点从内容知识、课程知识、学生知识、教学策略知识、评价知识等5个维度探讨新手与熟手教师PCK差异及差异形成的原因,并据此提出相关建议,为促进高中化学新手教师的快速专业化成长提供借鉴和参考。     

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。     

新手-熟手化学教师课堂教学基元系统有效性的比较研究

依据课堂教学系统CPUP模型理论和课堂教学基元系统有效评价量表,通过对24位新手教师和熟手教师的24节常态课堂中基元系统有效性进行对比分析。结果发现,新手教师与熟手教师的主要差别表现在“教学行为链实施质量”和“资源和技术的使用质量”2个维度上,熟手教师显著高于新手教师;而在“时间利用的合理性”“匹配度”和“基元内容的合理性”3个维度上,2者不存在显著差异。     

全日制化学教育硕士的PCK水平调查研究*

以美国埃里克森学院PCK量化工具为研究基础设计调查问卷,选取离子反应第1课时的电离概念教学片断,以河北某高校学科教学(化学)专业37名教育硕士为研究对象,要求被试者在对视频片断进行观摩的基础上作答9个开放性问题。研究发现:全日制化学教育硕士PCK整体和各维度知识处于“基本的”水平,在教学内容知识维度表现最佳,在学生知识、教学策略知识维度稍差一些,在把握概念关系、调整教学策略等能力活动上的表现有待发展。针对研究发现,结合化学教育硕士的专业属性及培养过程中的问题,提出构建“教师专业学习共同体”,干预化学教育硕士PCK结构的改善;依托教学案例情境载体功能,帮助化学教育硕士进行PCK的深度建构;开展基于研究性反思的教学实践,促进化学教育硕士PCK螺旋式提升等3条建议。     

“高端备课”前、中、后高中化学教师PCK发展变化的案例研究——基于原电池主题

深入到具体教学内容主题的层面,对学科教学知识（Pedagogical Content Knowledge,简称PCK）内涵构成和教师PCK的发展进行过程性研究。以北京师范大学化学教育研究所“高端备课”项目为平台,以《化学2》和《化学反应原理》的“原电池”主题为载体,提出PCK的分析框架,并据此开发调查问卷进行调查。结果表明教师在“高端备课”培训过程中,PCK的一级维度和二级维度均得到发展,其中学生学习知识和教学策略知识这2个一级维度的提升最为明显,电化学思维模型、学生认识发展特点、知识的功能价值和思路外显这4个二级维度的提升较为显著。教师普遍认为培训中的备课研讨环节和试讲反思改进环节,以及指导专家的分析讲解、质疑提问和讨论建议这3种指导行为是促使其PCK提升的主要原因。     

新手-熟手高中化学教师PCK个案比较研究* ——以“氧化还原反应”主题为例

采用访谈法与质性资料分析法,测查了6名(3名新手与3名熟手)高中化学教师关于氧化还原反应主题的PCK。结果表明:(1)新手教师与熟手教师在CTO,KoL与KoS组分上存在较明显的差异。新手教师倾向于采用“教师-传授”教学取向,对学生知识的把握相对不足,更强调使用习题巩固策略;而熟手教师倾向于采用“学生-建构”教学取向,对学生知识的把握更为全面,更强调学生自主建构知识的过程。(2)新手教师与熟手教师在KoC与KoA组分上存在较明显的相似之处。在课程知识方面,教师对课程标准与教材中氧化还原反应主题内容具有较好的理解,但对化学基本观念、学科核心素养认识尚浅;在评价知识方面,教师偏向于传统的评价方式,且集中在形成性评价和总结性评价,但相对缺乏对学生的课前诊断性评价。文末据此对我国化学教师教育及其研究提出相关建议。     

新手熟手初中化学教师课堂教学行为特征的比较研究*——以“酸和碱”单元教学为例

通过对新手化学教师和熟手化学教师各4节“酸和碱”单元常态课堂中教师使用教学行为链、教学行为对在时间和频次等方面的特征进行对比分析发现,在教学行为链上,新、熟手化学教师都会在较高水平的教学行为链上花费更多的时间,熟手化学教师高水平教学行为链在频次上的占比要优于新手化学教师,在不同教学行为链时间安排上的合理性要更高一些;在教学行为对上,新、熟手化学教师都多以“问”和“讲”,学生多以“答”的方式来展开课堂活动,熟手化学教师在每一次“动”和“思”上所用时间要明显高于新手化学教师,学生参与课堂的水平上,熟手化学教师要优于新手化学教师。得出如下启示:与熟手化学教师相比,新手化学教师应有效地组织和安排课堂教学行为,注重对“酸和碱”学科内容本身及其教学的驾驭。无论是熟手还是新手化学教师均应进一步给予学生课堂参与的机会。     

理科师范生使用课程材料的研究——以广州市某高校为例

利用“理科师范生使用课程材料情况问卷”,对广州市某高校167名理科师范生在教育实习期间使用课程材料的形态进行调查,发现理科师范生在各维度均表现出较好的课程材料使用形态,但未达到很高的水平。不同专业师范生的课程材料使用形态在“科学探究”“STSE”和“教师学习”维度存在显著差异;不同实习学校类型师范生的课程材料使用形态在“STSE”维度存在显著差异;不同实习年级师范生的课程材料使用形态不存在显著差异;有无家教经验师范生的课程材料使用形态在“科学探究”“STSE”和“教师学习”维度存在显著差异。文章最后提出理科师范教育的建议。     

国内外理科PCK理论研究的进展与启示

主要从概念框架、定义取向、组分界定、理论模型、学科与主题专属性等5个方面,对国内外理科（化学）PCK理论研究进行较系统地梳理。综述表明：（1）已有研究主要以舒尔曼的PCK概念框架为基础;（2）采用“静态结构观”或“动态建构观”的定义取向;（3）重视PCK组分的界定及其相互关系;（4）使用“整合型”或“转化型”理论模型诠释SMK与PCK的关系;（5）强调PCK的学科与主题专属性。文末基于国内外的研究进展,对我国化学PCK的理论研究提供相应的启示。     

高中化学新手熟手专家教师教学策略知识比较*

以“原电池”教学主题为载体自编调查问卷,选取河北省90位在职高中化学教师进行教学策略知识(Knowledge of instructional strategies,简称KoIS)测查。应用单因素方差分析与多重比较LSD法,从教学策略与表征的选择、应用、调整、反馈以及评价等5个维度对新手、熟手和专家教师KoIS之间的差异及其表现特征进行了比较和分析,并据此提出相关建议,为促进高中化学教师KoIS水平提升提供借鉴和参考。     

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%.     

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.     

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.     

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.     

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.     

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.     

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.     

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.