"PBL"模式下有机化学实验的教与学

结合化学实践教学特点,分析有机化学实验教学中存在的问题,讨论如何将"PBL"教学模式应用到"有机化学实验"教学中,形成"学生为主,教师为辅"的新型教学模式;同时探索思政教育融入有机化学实验课程的实践途径,提出在实践教学过程中,通过典型案例融入思政元素的具体方法,以"立德树人"为理念形成融会贯通、持续创新的新工科教育体系,加强学生的思想教育建设,系统推进大学组织模式、学科专业结构、人才培养机制和教师评价机制等方面的综合改革,构建一流卓越人才培养体系。     

农林大学“有机化学实验”课程教学的探索和实践

对农林大学“有机化学实验”课程教学的模式进行了探索.采用了第一课堂教学平台加第二课堂教学平台的教学模式.充分有效利用第一课堂平台的同时也积极拓展第二课堂的教学功能,既解决学时不足,又达到了教学目的.本课程教学模式的改革与实践给学生提供了个性发展的空间,满足了不同层次不同专业学生的需求,使学生建立了初步的科学研究的基本方法和思想.进一步激发了学生自主的、积极的思考意识,教学实践表明,新的有机化学实验体系的形成,综合性、设计性和开放性实验的开设,使有机化学实验课程更适合高素质人才培养的需要.     

有机化学实验混合教学模式的设计与实践

通过介绍混合教学模式在有机化学实验课程教学中的设计、实施情况及效果评价与反馈等内容,与大家分享混合教学模式在有机化学实验课程教学中的应用经验与思考。     

激励机制辅助的翻转课堂教学模式的应用——以有机化学实验为例

针对我校有机化学实验课程传统教学模式中存在的弊端,探索了激励机制辅助的"翻转课堂"教学模式,并以正溴丁烷的制备实验为例,介绍了课前、课中以及课后的教师和学生工作内容以及教学评价。实践表明:激励机制辅助的"翻转课堂"教学模式,极大地调动了学生自主学习的积极性和主动性,且激励机制可以更有效地保证"翻转课堂"的顺利实施。     

创新有机化学实验双语教学模式的探索与实践*

基于实践教学经验,从引导预习、优化课堂组织形式、撰写实验报告、改进考核方式等环节入手,开展了创新有机化学实验双语教学模式的探索与实践。创新教学模式可以充分调动学生学习的主动性和积极性,充分发挥任课教师的主导作用,培养了学生扎实的实验技能,提高了学生专业英语水平,增强了学生的创新意识和创新能力,有效地提升了有机化学实验课程的教学质量。     

翻转课堂模式在有机化学实验教学中的探索与实践

针对当前有机化学实验课程存在重讲授轻实验、重验证轻探究、重结果轻过程等弊端,学生积极性和主动性受抑制等问题,我们将翻转课堂模式应用于有机化学实验的教学中进行探索和实践。改变课前和课中学习方式,课前通过信息技术手段完成知识传授过程,课中师生研讨完成知识内化过程,将教学模式从"以教为主"转变为"以学为主",提高了学生的学习积极性、课堂参与度,培养了学生的自主学习、团队协作、表达交流等能力。我们发现翻转课堂模式下,学生在实验操作失败率、实验产物收率、实验报告质量、理论考试成绩等实验课程综合能力上获得提高,有机化学实验课程教学质量得到进一步提升。     

“翻转+分段式”有机化学实验教学设计及实践研究

以FeCl_3·6H_2O催化合成乙酸乙酯为教学内容,采用"翻转+分段式"混合教学方法对整个实验过程进行了改革探索。通过教师准备学习资源,学生自主学习,课堂分段讲解,互动交流以及跟踪评价等,探讨了大学有机化学实验实施"翻转+分段式"混合教学方法的有效途径。实践结果表明:混合教学模式能够显著促进学生对实验内容的理解和掌握,明显增加学生自主操作的时间,还能有效降低实验过程中的安全隐患。     

基于建构主义理论的有机化学实验混合式教学设计与实践*

基于建构主义理论和支架式教学思想,以“北京大学有机化学实验在线学习与测试平台”为依托,探索了混合教学模式在有机化学实验课程中的应用。以薄层色谱和柱色谱实验为例,通过确立目标、分析学情、分解任务、搭建支架、教学实施、评估反馈的教学设计和实践,帮助学生掌握实验知识与技术,培养学生解决实际问题的能力,增强其实验信心。     

“翻转+分段式”有机化学实验教学设计及实践研究

以FeCl3·6H2O催化合成乙酸乙酯为教学内容,采用“翻转+分段式”混合教学方法对整个实验过程进行了改革探索。通过教师准备学习资源,学生自主学习,课堂分段讲解,互动交流以及跟踪评价等,探讨了大学有机化学实验实施“翻转+分段式”混合教学方法的有效途径。实践结果表明:混合教学模式能够显著促进学生对实验内容的理解和掌握,明显增加学生自主操作的时间,还能有效降低实验过程中的安全隐患。     

基于“讲一练二考三”理念的有机化学实验教学改革

2015年南开大学提出了"讲一练二考三"新理念，旨在从教学方式、教学内容和考核方式等方面对本科教学进行改革，切实提高教学质量。"讲一"要求教师精讲决定实验成功的关键内容，强化学生主动学习能力；"练二"要求对实验内容进行合理安排，增加学生实践机会；"考三"则要求考试内容不限于教材内容，注重将学科前沿设计成考核内容。介绍了"讲一练二考三"理念在有机化学实验教学改革中的运用。教学实践表明该教学模式能够提高学生的学习主动性，有利于培养创新思维和实践能力。     

"Alpha"-, "beta"- and "delta"-anhydrodigitoxigenin

The syntheses of 3β-hydroxy-5β-carda-14, 20:22-dienolide (= «β»-anhydro-), 3β-hydroxy-5β-carda-8:14, 20:22-dienolide (= «α»-anhydro-) and «δ»-anhydro-digitoxigenin (= probably 3β-hydroxy-5β, 14β-carda-8, 20:22-dienolide) by the best ways known to date, have been described. «δ»-Anhydro-digitoxigenin represents the thermodynamically most stable isomer. In this isomer the double bond in position 8 is unaffected by hydrogenation with Pt in acetic acid; with perbenzoic acid an epoxide results from which, on hydrogenation, the double bond can be regenerated in its original position. Analogous reactions are known to occur in the 8:14-epoxides.     

化“材”为“筑”

Chemistry is a central, practical and creative discipline. The development of chemistry plays an important role in the progress of science and society, as well as the improvement of the quality of human life. This paper introduces the chemical knowledge of stone, concrete, glass and other inorganic nonmetallic building materials by the anthropomorphically story. Taking nanomaterials as an example, the prospect of building materials development in the future is put forward.     

Making "wheels" and "cubes" from triangles

[Mn(IV)Mn(II)3] triangular units directed by the presence of tripodal alcohols self-assemble in the presence of azide and acetate ligands to form either a [Mn24] "wheel" or a [Mn32] "cube".     

"Turn-on" fluorescent sensing with "reactive" probes

Chemical probes are valuable tools for the investigation of biochemical processes, diagnosis of disease markers, detection of hazardous compounds, and other purposes. Therefore, the development of chemical probes continues to grow through various approaches with different disciplines and design strategies. Fluorescent probes have received much attention because they are sensitive and easy-to-operate, in general. To realize desired selectivity toward a given analyte, the recognition site of a fluorescent probe is designed in such a way to maximize the binding interactions, usually through weak molecular forces such as hydrogen bonding, toward the analyte over other competing ones. In addition to such a supramolecular approach, the development of fluorescent probes that sense analytes through chemical reactions has witnessed its usefulness for achieving high selectivity, in many cases, superior to that obtainable by the supramolecular approach. Creative incorporations of the reactive groups to latent fluorophores have provided novel chemical probes for various analytes. In this feature article, we overview the recent progress in the development of turn-on fluorescent probes that are operating through chemical reactions triggered by target analytes. Various chemical reactions have been implemented in the development of many reactive probes with very high selectivity and sensitivity toward target analytes. A major emphasis has been focused on the type of chemical reactions utilized, with the hope that further explorations can be made with new chemical reactions to develop reactive probes useful for various applications.     

"Decoking" of a "coked" zeolite catalyst in a glow discharge

'Decoking' of a 'coked' zeolite catalyst in a glow discharge in oxygen is investigated. The 'decoking' process involves reactions of atomic oxygen (O atoms) with 'coke' and yields gases such as CO, CO₂ as well as other gaseous products that could be easily pumped out.Three different modes of discharge were investigated including a static mode, a flowing-gas mode, and a periodic-purge mode where the oxygen and other gaseous products of the discharge were replaced by fresh O₂ gas after short but regular intervals of time. In some cases, additional heating was also used to provide base temperatures of the order of 100 °C to facilitate penetration of oxygen atoms into the inner layers and cages of the zeolite catalyst.This paper presents some results of spectroscopic analytical techniques used to monitor the atomization of oxygen, oxidation of 'coke', and to confirm the process of 'decoking'. More specifically, radiation emission on the 3 s ⁵S– 3p ⁵P transitions of O around 777.2–777.5 nm were selected for monitoring the atomization of O₂. On the other hand, X-ray photo-electron spectroscopy (XPS) was used to determine the amount of residual carbon and extent of 'decoking'. Furthermore, evolution of CO and CO₂ gases as a function of time was systematically monitored in real time. For CO, the 451.1 nm band head belonging to the B¹ - A¹ bands of the Angstrom system of the CO spectrum was used, while for CO₂, the band head at 353.4 nm belonging to the CO₂⁺ spectrum was used. The rates of evolution of CO and CO₂ were related to the rate of 'decoking' of the catalyst. It is noted that in the periodic-purge mode, about 63% of the total yield of CO from a given sample of the catalyst appears in the first 3-min exposure to discharge whereas it takes up to 15 min to remove nearly 94% of the removable carbon under our experimental conditions.     

营养化学课程翻转课堂的探索与实践

With its tailored learning content, flexible learning environment and directed teacher guidance, the flipped classroom in "nutrition chemistry" has effectively solved the problems of students' specialty, large number and limited time in the course of elective course. The teaching mode based on the cultivation of students' ability and the core of improving scientific literacy was constructed.     

Size evolution study of "molecular" and "atom-in-cluster" polarizabilities of medium-size gold clusters

A study on static polarizabilities for a family of gold clusters (Au(n), n = 6, 12, 20, 34, 54) is presented. For each cluster, a density functional theory perturbation theory calculation was performed to compute the cluster polarizability and the polarizability of each atom in the cluster using Bader's "quantum theory of atoms in molecules" formalism. The cluster polarizability tensor, α(cluster), is expressed as a sum of the atom-in-molecule tensors, α(cluster)=∑(Ω)α(Ω). A strong quadratic correlation (R(2) = 0.98) in the isotropic polarizability of atoms in the cluster and their distance to the cluster center of mass was observed. The cluster polarizabilities are in agreement with previous calculations.