“素养为本”的高中化学课堂教学评价标准研究

为落实《普通高中化学课程标准（2017年版）》所倡导的“重视开展‘素养为本’的教学”理念,需要开发与之相适应的高中化学课堂教学评价标准体系。围绕“素养为本”的高中化学课堂教学在教学设计、教学活动、思维过程、素养达成等方面的核心要素,形成了以1个核心、4个维度、20项指标为基本框架的课堂教学评价标准体系,并采用专家咨询、课例检验等方法使该评价体系更趋科学、全面、规范。     

核心素养框架下浙江省高中化学学业水平试题特征研究

从高中化学核心素养的5个维度出发,构建了评估化学学业水平试题特征的分析框架,对4份浙江省高中化学学业水平试题展开了研究。结果表明,浙江省高中化学学业水平试题在广度上基本涵盖了核心素养各维度的考查,在深度上对核心素养各维度的考查总体处于中游水平,“科学精神与社会责任”维度的考查所占比重过小,核心素养各维度高水平层次要求的考查所占的比重较小等。     

真实情境与化学学科核心素养的发展——基于《普通高中化学课程标准(2017年版)》的解读

《普通高中化学课程标准（2017年版）》构建了化学学科核心素养的内容体系及其发展水平框架,重视开展“素养为本”的教学,重视真实情境的创设。在分析教学情境的内涵与功能的基础上,解读了新课标中课程内容、实施建议和命题原则中对真实情境创设与应用的要求,讨论了真实情境在发展学生化学学科核心素养中的教育价值。通过对具体教学案例的分析,探讨了基于学生化学学科核心素养发展的教学情境设计的策略。     

基于培养学生核心素养的“高分子化学”课堂教学设计——以“体型缩聚和凝胶化作用”为例

将核心素养元素与《高分子化学》课程教学有机结合，使学生学会专业知识、掌握专业技能，同时形成适应社会发展需要的品格和关键能力。本文以“体形缩聚和凝胶化作用”为例，围绕本节知识和能力培养目标，对课堂教学进行了设计。通过类比联想、分析对比、感悟体会等融入与专业知识契合的“人文素养、科研精神、责任担当”等素养元素。对核心素养与高分子化学课程教学相融合的实施效果进行了浅析，同时对如何在课程教学过程中培养核心素养进行了探讨反思。     

基于化学学科理解的电化学主题认识模型研究*

在核心素养导向的化学教学实践新时代背景下,基于化学学科理解构建相应主题的认识模型,提升教师的化学学科理解水平,进而开展素养为本的课堂教学促进教师专业发展,为化学教育理论和实践研究提供了重要的思路和方向。以电化学主题为例,基于化学学科理解构建其认识模型,以期其研究思路和过程对化学学科其他主题的理论和教学研究具有启示作用。     

促进学生建立认识角度的化学课堂教学行为研究

为了探寻促进学生建立认识角度的有效教学行为，构建了由教学环节、教学子环节和具体教学行为等3个维度构成的分析框架，选取有代表性的教学课例，依据分析框架对教学课例进行编码。通过深入对比分析优秀常规课例与促进学生建立认识角度的课例的教学行为，得到了促进学生建立认识角度的有效教学行为。     

化学理论课堂教学结构模型构建初探——基于课堂教学视频案例分析的研究

模块化结构的我国中学化学课程标准和新教材,需要寻求教学规律与课堂教学的组成、结构模型来支持课程目标的实施,将课堂教学视频案例研究作为新的研究方法,成为关注的热点。研究采用了课堂教学视频案例采集和教学结构维度的分析方法,选取了6个优秀化学理论课堂教学视频案例,应用“Videograph”视频分析软件从学生学习行为、教师教学行为和师生互动3个主要维度对案例进行分析、解读与比较。对教师课堂导入、新内容讲授（区分为教师启发式讲授和教师直接知识讲授）、师生课堂探究（区分为教师演示实验探究和学生自主探究）、师生课堂探究讨论（区分为学生小组探究讨论、师生互动问答讨论）、课堂练习、课堂小结、其他活动等7个部分进行了编码分析和特征解读。初步提出了化学理论课堂教学结构的时间模型。     

“素养为本”化学课堂教学展示讲解行为的价值及实施策略研究*

展示讲解行为在“素养为本”化学课堂教学实践中具有独特价值,能够创设建构性的化学教学情境,能够提供化学核心概念建构的证据,能够提供学生核心素养表现的机会。因此,教师应基于发展学生化学学科核心素养这一主旨,在实施展示讲解行为时采取以下教学策略:设计真实且富有价值的问题,运用多种有效协同展示形式,设计多样的高阶思维活动。     

核心素养背景下化学教材中人文意蕴的分析与启示*——以美国教科书《化学:概念与应用》为例

针对当代核心素养背景下学科核心素养中人文向度的部分缺失,以美国主流理科教科书《化学:概念与应用》作为研究对象,选取了4则人文意蕴特征明显、内涵丰富的“跨学科”栏目典型案例,通过对其人文意蕴向度的结构性与教学价值分析,获得学科人文智性及其教育的启示:以科学与人文的对话推动2个世界的沟通;以科学的革命性突跃弘扬科学精神的人文光辉;倡导自然与艺术和谐统一的人文审美意向;肩负社会责任与维护和平正义的进步人文思想。 为学科教学中人文教学资源的研究开发提供认识导向;为完善当前学科核心素养内容提供参考;并从选材理念、教学准备、课程教学、目标达成4个方面为该类资源的教学应用提供策略建议。     

素养导向的高中化学项目教学中教师有效行为研究——以“探秘神奇的医用胶”项目教学为例

以“探秘神奇的医用胶”为主题设计实施了素养导向的项目教学。从教师行为的角度,对本次项目教学的课堂录像编码分析,发现本次项目教学的3个关键过程、7种高频行为类型、7种高频和次高频问题类型。根据编码结果回顾课堂录像,分析讨论教师在项目教学中如何通过高频行为类型、高频和次高频问题类型帮助学生建立有机物和有机反应的认识角度和认识思路,促进学生化学学科核心素养的发展。     

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.