新课程背景下开封市高中学生化学学习自我效能感调查

以新课程背景下河南省开封市区327名高中生为被试,以《高中生化学学习自我效能感量表》为测量工具,运用SPSS16.0对数据进行统计分析,调查高中生化学学习自我效能感水平,探讨不同性别、年级以及成绩水平的高中生在化学学习自我效能感上的差异。研究结果表明：）1）高中生化学学习自我效能感水平一般;）2）高中生化学学习自我效能感存在显著的年级差异,高一学生的化学自我效能感显著低于高二、高三年级,性别差异不显著;）3）高中学生的化学学习自我效能感与化学学习成绩呈显著正相关,且不同成绩水平高中生的化学自我效能感差异显著。根据被调查高中生化学学习自我效能感水平及特点进行了讨论,并提出了一些有针对性的教育教学建议。     

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。     

化学学科中学生自我效能感的调查分析

本研究以石家庄市3所不同层次中学的472名高中生为研究对象,采用自我效能感综合量表以及自编问卷进行了问卷调查,探索了不同学校、不同年级、不同性别的高中生在学习化学学科中的自我效能感的基本特点,提出了有针对性的教育教学建议。     

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。     

“动手—动脑”教学中教师自我效能感的调查研究

“动手—动脑”教学是适应新课程改革的一种全新的课堂教学模式。教师自我效能感是教师对自己教育教学能力的一种认知和信念。“动手—动脑”教学中教师自我效能感的取向将直接影响教师的教学行为,进而影响课堂教学改革的深度与广度。在谈话、问卷调查的基础上分析“动手—动脑”教学中教师自我效能感的现状以及影响自我效能感的主要因素。对获得的数据结果利用spss13.0进行统计分析。     

高三学生化学学习自我效能感现状的调查研究

将化学学习自我效能感界定为3个一级维度、11个次级维度, 自编问卷, 对北京市大兴区一所普通高中150多名高三理科学生的化学学习自我效能感水平的现状进行了调查。运用SPSS 19.0和Excel 2007软件对调查数据进行处理, 分析了导致学生化学学习自我效能感偏低的原因, 提出了相应的教学策略。     

高中生化学学习动机、学习效能感与学习成绩的关系调查研究

通过借鉴和优化国内外学习动机、学习效能感与学习成绩的关系问卷,调查了武汉某中学220名高二学生化学学习动机和学习效能感与学习成绩的关系。通过对回收问卷进行描述性统计、t检验、相关分析和中介效应检验等,得出以下结论：（1）高中生化学学习动机和学习效能感均处于中上等水平,其中化学学习动机由内部动机和外部动机共同主导,学习效能感由学习能力效能感主导。（2）不同性别学生在内部动机和学习效能感及各维度上存在显著差异,且表现为男生得分普遍高于女生;不同班级学生在化学学习动机、学习效能感及各维度上均无显著差异。（3）高中生化学学习动机、学习效能感和学习成绩及其各维度间均存在显著的正相关。（4）高中生的学习效能感在化学学习动机和学习成绩间有部分中介效应,具体效应值为0.132,且学习效能感2个维度中的学习能力效能感（效应为0.131）与学习行为效能感（效应为0.132）的中介效应相当。     

高中生化学学业求助行为、学业自我效能感与化学学习焦虑的关系：个体中心的视角

采用潜在剖面分析和多项Logistic回归分析方法,探索1 092名高中生化学学习焦虑的潜在类别,以及学业求助行为和学业自我效能感对不同类别化学学习焦虑的影响。结果表明：高中生化学学习焦虑存在3个类别,分别是C1组(低化学学习焦虑)(23.81%)、C2组(中等化学学习焦虑)(57.60%)和C3组(高化学学习焦虑)(18.59%);高中生的执行性求助和回避求助得分越高、工具性求助和学业自我效能感得分越低,越容易被分到C2或C3组,而不易被分到C1组。     

初中化学用语的教学目标研究

以初中生化学用语测试、问卷调查、学生访谈、教师访谈和课堂观察等方面测查分析为依据,找出学生学习和教师教学中的主要问题。为了解决这些问题,开展了对初中化学用语教学目标的研究,编制了初中2个学段化学用语的教学目标。用具体的课堂教学案例,研究落实教学目标的方法。     

增强大学生学习自我效能感的化学实验教学策略*——以“药物制剂工程实验”为例

以提高大学生化学实验积极性和实验学习效率为目标,在“药物制剂工程实验”课程中实施能增强大学生学习自我效能感的化学实验教学策略。以“乳剂的制备”实验为研究背景,设计并实施了三阶段的实验教学流程。同时,通过构建过程性评价量化指标、开展三方评价和问卷调查等形式,对该化学实验教学策略的实施效果进行了评价。通过对比实验组和对照组学生的过程性评价成绩和问卷调查结果,发现实验组平均得分大多高于对照组,说明采用了本实验教学策略的实验组学生的自我效能感高于对照组,因此,本实验中采取的提高大学生自我效能感的化学实验教学措施确实有效且具有实际意义。     

充满生机和科学机遇的磷化学研究所

简要地综述了第十五届国际磷化学会议的报告内容，介绍了目前磷化学的主要 研究领域，包括不对称合成、配合化学，生物碱化学，药物化学，农业化学等相关 领域的研究动态及新进展。     

Novel arylpyridine‐based 1,3,4‐oxadiazoles: Synthesis,antibacterial, and anti‐inflammatory evaluation

In view of developing novel bioactive compounds, a series of 2‐(5‐[2‐methyl‐6‐arylpyridin‐3‐yl]‐1,3,4‐oxadiazol‐2‐ylthio)‐1‐arylethanones (6a–n) were designed and synthesized in good yield. Novel compounds were evaluated for their antibacterial and anti‐inflammatory activities. All synthesized compounds were screened for their antibacterial activity against Staphylococcus aureus, Bascillus subtilis, Eschericia coli, and Pseudomonas aeruginosa strains. Compounds 6a , 6b , 6c , 6h , and 6i displayed the highest antibacterial activity with minimal inhibitory concentration (MIC) values ranging from 6.25–12.5 μg/mL in comparison with the standard Ciprofloxacin. The results of anti‐inflammatory activity of carrageenan‐induced footpad edema assay indicated that tested compounds exhibited remarkable anti‐inflammatory activity with percentage of inhibition of 63.9–70.1% (potency 96.8–106.20% of indomethacin activity) after 3 hr. Particularly, 6c – e and 6j – l were found to be excellent inhibitors of inflammation, with potential higher than that of the standard, Indomethacin.     

Novel [1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives embedded with benzimidazole moiety as potent antioxidants

Fourteen novel [1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivatives bearing benzimidazole moiety ( 7a-n ) have been synthesized using the one-pot nitro reductive cyclization method. All the synthesized compounds were confirmed by ¹H nuclear magnetic resonance (¹H NMR), ¹³C NMR, fourier-transform infrared (FT-IR), mass spectrum, and elemental analyses. All the title compounds were subjected to in vitro antioxidant activity. The free radical scavenging activity of the compounds was examined using DPPH, nitric oxide, and superoxide radical scavenging methods. The results demonstrated that compound 3-(2-(3,4-dimethoxyphenyl)-1-propyl-1H-benzo[d]imidazol-5-yl)-6-4-tolyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine ( 7c ) was potent in scavenging both DPPH and nitric oxide radical with IC₅₀ values of 13.57 and 18.55 μg/ml when compared to the standard with IC₅₀ values of 23.75 and 23.14 μg/ml, respectively, which was due to the presence of electron-donating groups. The activity was found to decline when electron-donating groups were replaced by electron-withdrawing groups. Moderate scavenging activity was observed for the superoxide radical. Structure activity relationship and physiochemical properties were studied for all the derivatives.     

Dual zinc catalysts for L‐lactide polymerization and reaction of CO2 with cyclohexene oxide

A series of zinc complexes, [ L ^X ZnEt] ( 1–5 ) and [ L ^X Zn ₂ (OAc) ₃ ] (6–9) , associated with NNO‐tridentate Schiff base ligands (2‐(((2‐((cyclohexyl[methyl]amino)methyl)phenyl)imino)methyl)phenolate (CAP) derivatives), were synthesized, and their activity toward ring‐opening polymerization (ROP) of L‐lactide (LA) and the reaction of CO₂ with cyclohexene oxide were also investigated. All of [ L ^X ZnEt] revealed excellent catalytic activity to ring‐opening polymerization (ROP) of LA in the presence of benzyl alcohol. Among them, [ L ^H ZnEt] (1) showed the highest activity with 82% conversation within 45 s. In contrast, [L ^X Zn ₂ (OAc) ₃ ] (6–9) were inactive in ROP of L‐lactide. In addition, all of these Zn complexes demonstrated moderate activity in the reaction of CO₂ with cyclohexene oxide in the presence of Bu₄NCl.     

Exploring recent developments on 1,2,4-triazole: Synthesis and biological applications

Triazoles are nitrogen-bearing heterocycles. In the last few decades, researchers have focused on fused heterocycles, as they have better pharmacological effect compared to triazoles alone. Among the two isomers of triazole, this article aims to explore the work carried out on 1,2,4-triazole and N-bridged heterocycles derived from 1,2,4-triazole in last 18 years, highlight different synthetic pathways, and present a brief summary of the different biological activities possessed by 1,2,4-triazole derivatives. The information collected in this article is expected to help researchers to discover novel therapeutic agents for better applications in the field of pharmaceutical science.     

Biologically inspired 3Fe4S cluster as structural mimics of FeMoco M-cluster

A 3Fe4S cluster related to M-cluster of Mo-nitrogenase is reported. [K(THF)₅][Fe₃(μ-bdt)₂(μ-PPh₂)(CO)₅] ( 1 ) is synthesized from photo-assisted structural rearrangement of [K(THF)₂][(μ,κ²-bdt)Fe₂(μ-PPh₂)(CO)₅] under visible light irradiation. The molecular structure of 1 consists of a Fe₃ core bearing one dithiolate bridge and the second dithiolate group capping onto the metallic plane. The structural motif of 1 is analogous to that of Mo-participated 3Fe4S unit in M-cluster of Mo-nitrogenase, with the similar Fe-Fe and Fe-S bond distances. Upon protonation in 193 K, a Fe-hydride species ( 1H ) is generated and characterized to possess the bridging hydride group (δ = −12.57 ppm) by ¹H-NMR spectroscopy and DFT calculation. In CH₃CN solution, complex 1 exhibits a reversible reduction and oxidation process at $E_{1/2}^{\mathrm{red}}$ = −1.94 V and $E_{1/2}^{\mathrm{ox}}$ = −0.18 V, respectively, at 273 K. The reduction behavior of 1 in CH₂Cl₂ solution at 243 K displays a slight modification in the presence of trifluoroacetic acid, revealing a moderate anodic potential shift (~50 mV). The current amplitude of the reduction wave is linearly increased with the increasement of acid added, indicative of the catalytic event.     

环戊二烯类有机金属含硫族化学的新进展

本文系统地综述了环戊二烯类有机过渡金属含硫族(S, Se, Te) 化学领域的研究现状和进展。参考文献136 篇。     

化学学科的新视角及其在化学教育中的反映

传统化学以研究变化,关注变化前后的结果而著称。化学与其他学科,特别是生命科学的相互渗透使得化学的动态特征更加突出,化学学科格局也因之发生了变化。因此,化学需要新认识。     

Meeting the sustainable development goals in a tropical climate

This article reflects on the Federation of Asian Chemical Societies (FACS) Citation Award Lecture delivered in the Industrial Technology Research Institute Symposium on CO₂ Utilization and Green Technology during the 18th Asian Chemical Congress held in Taipei, December 12, 2019. Malaysia produces sizable amounts of palm oil and palm kernel oil, with palm fronds and tree trunks as the main waste. At the Malaysia Japan International Institute of Technology, the biomass was decomposed to produce fine chemicals, used as substrate for mushroom growth, and converted to bio-coke for heat energy. A notable difference has been found regarding the emission of greenhouse gases from a natural peat forest and those from the oil palm plantation converted from peatlands, where in the palm plantation, water table is lowered and aerobic processes occurs, resulting in more CO₂ being released compared to CH₄. The introduction of fertilizers to the plantation resulted in more N₂O being released. The team has also pioneered a project to plant temperate vegetables. Cooling pipes (16–18°C with circulating water cooled by chiller) were embedded within each thermal conditioning soil plot. Lettuce and radish, the experimental plants, showed good growth in the thermal conditioning soil due to nitrogen-fixing bacteria, which were destroyed at a higher temperature.     

有机化学进展(2011~2012)

本文综述了中国大陆地区有机化学研究人员2011至2012年两年内在合成方法学、有机合成化学、元素有机化学以及天然产物化学等领域获得的重要成果。文章中共引用参考文献355篇,其中110多篇手性金属配合物和有机小分子催化的不对称反应、金属催化的碳氢键活化等合成方法学论文和30余篇氟有机化学论文基本来源于德国《应用化学》(国际版)和《美国化学杂志》。本文汇集了中国有机化学家两年中合成的150多个具有生物活性和化学结构多样性的天然产物,其中不乏具有高度挑战性的复杂天然分子。在近两年中中国有机化学家从陆地和海洋的生物体内发现各种不同类型新天然产物90多个。