中学生化学学业成败归因与自我效能感研究

运用中学生化学学业成败归因量表和学业自我效能感量表,抽取653名城乡中学生进行测查,对测查数据进行分析得出以下结论：中学生化学学业成败倾向于外部归因;城乡之间中学生化学学业成败归因、学业自我效能感存在显著差异;学业成败归因和学习行为自我效能感通过学习能力自我效能感这一中介变量影响学生的化学学业成绩。     

基于OBE理念的无机及分析化学“金课”建设探索与实践*

本着OBE理念,教研组确定了“以学生为中心,注重能力和素质培养,教学相融”的教学理念。根据课程内容和特点,以“金课”为标准,依托“超星学习通”线上平台,从线上线下教学分配、多样化互动课堂设计和实施、考核评价和持续改进等方面进行探索和实践。旨在培养学生自主学习能力,提高学生分析、解决生产实践问题的能力,以及树立学生团队协作意识,使知识性人才培养向知识、能力、素质三位一体型人才培养转变。     

大学生的化学自我效能感对自我调节学习策略及学业成就的影响研究*

大学生的学业成就是衡量高等教育质量的重要因素之一。由社会认知理论、建构主义学习和人本主义学习理论可知,高校大学生的化学自我效能感应能促进自我调节学习策略的运用,对学业成就与综合素质提升具有积极效应,但仍需要进行验证。故本研究目的:探讨高校大学生的化学自我效能感对学业成就的影响性,并考察自我调节学习策略的中介作用。研究方法:采用大学生的化学自我效能感量表、自我调节学习策略量表、化学专业学业成就量表等工具,通过整群抽样的方式,对国内某高校的536名化学化工专业大学生进行问卷调查。研究结果显示:大学生的化学自我效能感与化学专业学业成就显著正相关;大学生的化学自我效能感与自我调节学习策略显著正相关;自我调节学习策略与化学专业学业成就显著正相关;自我调节学习策略在化学自我效能感与化学专业学业成就之间起部分中介效应。     

“教、学、评”一体化的化学课堂教学评价目标设计

精准设计评价目标是有效开展教学评价,实现“教、学、评”一体化的前提和保证。化学课堂教学评价目标的制订需要围绕教学目标合理规划学习任务和学习活动,依据学习活动承载的素养功能和水平,结合相关学业质量水平的要求,准确定位评价角度和评价水平。以“物质的量及其单位--摩尔”课时教学为例来说明评价目标的科学制订和规范表达。     

整合FLOWMAP与SOLO分类理论的化学学习评价——以“化学平衡”为例

基于FLOWMAP和SOLO分类理论对高中生“化学平衡”认知结构进行测查并评价其学习水平,研究表明：学优生的认知结构中对“化学平衡”概念内涵的认知较为清晰和丰富;学生认知结构变量（广度、丰富度）与其纸笔测试成绩呈现显著的正相关;学生对化学平衡知识体系中6个主要概念的学习水平的差异较大,尤其对“压强因素”的认知较差;学生容易忽视化学平衡常数,并且对各影响因素进行科学推理时论证的严谨性较为缺乏,认知不全面且抽象性水平不高。     

高二学生认知结构、学科核心素养及学习困难的测量——以“卤代烃”为例

基于FLOWMAP测查高二学生"卤代烃"认知结构,并采用学科核心素养探究学生"卤代烃"学习困难。研究表明,学优生认知结构的优势体现在较高的认知"整合度"和准确率,学困生的劣势体现在较低的信息检索效率,学优生更善于运用描述及情境推理等信息处理策略建构知识。学生达到不同素养水平的学业要求差异较大。学习困难主要有不知道卤代烃的分类及物理性质,不明白或混淆发生取代反应与消去反应的特征、条件等,不知道卤代烃的用途。     

“化学游戏教学”的“学教评产”混合式教学模式实践

基于师范类专业认证理念与毕业要求的教学前端分析,建构“学教评产”混合式教学模式,通过整合教学内容、重构教学安排与优化教学评价,对“化学游戏教学”课程进行创新性改革,并从学生学习成果、教学目标达成与学生满意度等3个方面评价教学成效。结果表明:该教学模式有助于学生学习成果质量的提升,能够有效促进教学目标的达成,并取得较高的学生满意度。     

高一学生化学学科自我概念与学业成绩的关系

运用化学自我概念问卷,对高一学生化学学科自我概念和化学学业成绩之间的关系进行探讨,结果表明:学生化学学科自我概念达到中等水平,化学学业自信较高,化学学业自我调控较弱;学生化学学科自我概念水平在性别上无显著差异;父母职业背景对学生化学自我概念有较大的影响;学生化学成绩与化学学科自我概念得分之间具有一致性,学生化学成绩对化学学科概念的形成有显著的影响.     

初中化学(科学)启蒙教材中“实验”“插图”“科普知识”的比较分析*

我国大陆和台湾的化学(科学)教材在化学启蒙方面的内容编写有着各自的特点和优势,因此以我国大陆人教版初中《化学》与我国台湾康轩文教版《自然与生活科技》为例,通过问卷调查法与对比分析法,研究化学启蒙阶段的学生对待化学的态度以及海峡两岸教材中“实验”“插图”“科普知识”等3部分内容的设置差异。结果表明:(1)化学实验是启蒙阶段学生对化学感兴趣的起始点,也是初接触时的难点,其中以我国台湾《自然与生活科技》教材中化学实验的探究性及层次性更深;(2)化学启蒙阶段教材中插图的科学性、清晰度以及精美程度对学生学习化学的兴趣和态度有较大影响;(3)化学教材中的模型图实物化有助于学生拨云见日,了解化学的真实模样。     

体现“两性一度”的无机化学卤族元素课程设计*

基于对“两性一度”的科学理解,认为“卤族元素”课程设计的改革应将“如何切实体现‘两性一度’”作为重点突破方向较为合理。比较旧教材,这里应在注重核心内容主线突出、进行内容结构重组、发展学科融合作用和充分发挥教育功能等4个方面下功夫。新的讲授内容应是以利于促进学生科学素养发展的视角为出发点,突出创新思维和科学研究方法,以教师好使用、学生好自学为努力方向,以提高教学质量促进人才培养为目标实施“两性一度”。改革目的在于通过学习卤族元素后, 使学生在获得基础知识的同时,能学到些许科学的思想方法、学习方法和研究方法。     

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%.     

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.     

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.     

Selective syntheses of 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones via temperature-dependent Rh(II)-carbenoid-mediated 2H-azirine-ring expansion

The Rh(II)-catalyzed reaction of 2-carbonyl-substituted 2H-azirines with ethyl 2-cyano-2-diazoacetate or 2-diazo-3,3,3-trifluoropropionate provides an easy access to 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones. These compounds can be selectively prepared from the same starting material using temperature as the only varied parameter. The 2-azabuta-1,3-diene intermediate, a common precursor for both heterocyclic products, isomerizes into 2H-1,3-oxazine under kinetic control, while 1H-pyrrol-3(2H)-one is the sole product of the reaction at elevated temperatures. According to DFT-calculations a one-atom oxazine ring contraction involving ring-opening to a 2-azabuta-1,3-diene intermediate, followed by a 1,5- and 1,2-prototropic shift leads to the consecutive formation of imidoylketene and azomethine ylide, which then further undergo cyclization to the pyrrole derivative.     

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.