基于问卷调查的ATDE创造性思维教学模式探讨

ATDE创造性思维教学模式是以学生为主体,以教师为主导,通过“问、想、做、评”四个环节引导学生共同完成教学任务,旨在培养学生创造性思维的一种创新的教学模式。为了解学生对“大学化学”及实验教学中教学模式的态度,探讨应用ATDE教学模式的教学效果及影响因素。对九江学院2010级应用化学本科41名学生进行了回顾性问卷调查。结果表明,实施ATDE教学模式对培养大学生综合素质有显著的积极影响,大部分学生对ATDE教学模式很感兴趣,并且认为应用ATDE教学模式教学很有必要。同时针对实施过程中尚存的有关问题,提出了建议性的解决策略。     

基于翻转课堂-PBL的混合式“金课”教学*——以“药物分析”为例

以创新应用能力及岗位需求重构课程标准,更新教学方法和教学手段,从教学设计、教学实施、教学评价、教学效果等4个方面系统地探索了基于翻转课堂-PBL教学的药物分析课程教学模式建设与应用,旨在形成多元化、多层次的药物分析教学新体系,将“以教师教为主”的教学模式转变为“以学生学为主”,让学生化“被动”为“主动”学习,锻炼学生自主学习能力,增强学生团队协作及分析解决问题的能力,启发学生创新应用能力。     

线上线下互动教学模式在医学院校基础化学教学中的应用——以“缓冲溶液及其作用机制”为例

为提高基础化学的教学效果,以“UMU互动”为平台,开展线上线下混合式教学模式改革。以“缓冲溶液及其作用机制”教学设计为例, 阐述线上线下混合教学模式的应用。结果表明,混合式教学模式可以激发学生的学习兴趣,提升学生自主学习的能力,有效提高了教学质量和教学效果。     

基于雨课堂平台的化工基础“对分课堂”教学模式的探索与实践*

依托雨课堂教学平台,应用现代信息技术,在化工基础课堂教学中引入“对分课堂”教学理念和教学模式。以流体流动教学内容为教学案例,具体说明“对分课堂”教学模式的具体实施过程。实践结果表明,该教学模式激发了学生的学习兴趣和主观能动性,提高了课堂教学效果,有利于学生对化工基础知识的掌握、学生综合能力的培养和后续生产实践的应用。     

化学制药工艺学在线教学实践与思考

以化学制药工艺学课程为例,从在线教学技术、教学设计等方面探讨了以学生为中心的在线教学模式与方法,对比分析了在线教学与线下教学的优缺点.实践表明,与线下教学相比,以学生为中心的在线教学模式更有利于学生自主学习能力的培养和课程目标的达成.     

线上线下混合式教学结合翻转课堂进行酯缩合反应的教学*

采用“线上线下混合式教学”开展有机化学课程的教学工作,利用APP “学习通”将在线课堂教学和线下讲授相结合。以知识点酯缩合反应的教学为例,介绍了该教学模式的实施过程和教学效果。实践结果表明,线上线下混合式教学与翻转课堂相结合的教学模式,能够拓展化学专业学生知识面,提升学生的自主学习能力和学习的积极性,取得了较好的教学效果。     

“一体三翼”教学模式在工科无机化学教学中的应用与实践*

为适应当前复合型人才培养需求和提高学生自主学习能力和创新意识,在对大学一年级新生进行无机化学教学时需坚持以学生为主体的教学理念,并努力同时提高他们的思想政治素质、理论联系实际能力和科学研究素养。为此,提出“一体三翼”教学模式。然而,大多数工科院校无机化学课程的授课学时有所压缩,这对任课教师来讲是一种巨大挑战。通过“线上-线下”混合式教学解决学时不足问题,并通过学生课程参与度、学生学习成绩及教学反思等形式检验“一体三翼”教学模式的教学实践成效。     

在化学教学中以Blending Learning为理念尝试"双主-探究"教学模式的研究与实践

阐述了以Blending Learning为教学理念,通过构建学科教学网站实施"双主—探究"教学模式的研究。"Blending Learning"是当前国际教育理念发展的最新动向。而在教学中实施教师主导作用和学生主体地位的有机统一、以学生自主探究为主线的教学模式,是我们在经历了对传统教学模式的批判与继承及对建构主义教学理论的发扬与引申后建立起的一种科学的教学模式。     

观摩美国田纳西大学物理化学教学得到的启示

阐述美国田纳西大学物理化学课程教学的教学内容、教学方式、学生成绩的评估方式以及对教师教学工作的评估方式,并对比我国华南理工大学的物理化学教学,提出了借鉴美国高校物理化学教学的先进经验,将以教师为中心的教学模式转变为以学生为中心的教学模式是提高物理化学教学效果的一个有效途径。     

应用型本科院校有机化学实验教学改革实践与探索

以建构主义理论为指导,牢固树立以学生为主体、教师为主导的教学理念,对教学内容、教学方法、教学手段、教学模式和考核评价等进行全方位的教学改革和探索实践,建立“校企融合”“工学交替”和“产学研用”一体化教学模式,充分调动了学生的实验积极性、主动性和创造性。同时,通过强化实验基本操作技能训练,不断提高学生的综合实验设计能力、创新能力和科研能力,取得了良好的实践效果,为学生就业、创业奠定了坚实的技术基础,较好地满足了企业对高素质技术技能型人才的需求。     

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.     

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.     

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.     

A carbanion induced synthesis of highly congested pyrazole and imidazole containing heterocycles

An efficient approach to the synthesis of highly congested di, penta and hexacyclic pyrazoles as well as imidazole fragment containing novel heterocyclic molecule has been developed through a carbanion induced transformation of suitably functionalized 2H-pyran-2-ones, benzo[h]chromene and thiochromeno[4,3-b]pyrans. Due to the presence of fluorescence, we report their prime application metal sensor as off/on switching in ferric ions.     

Synthesis of pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles by Curtius reaction in Morita-Baylis-Hillman derivatives

Synthesis of substituted pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles from the Morita-Baylis-Hillman derivatives of acrylates via saponification followed by Curtius reaction is described.     

正丁胺对激光染料荧光谱影响的研究

用正丁胺作为碳源,采用射频辉光放电制备碳膜,选用激光染料R6G和聚乙二醇混合液作为蒸气源,采用单源热蒸发,在蒸发室与染料同时沉积得到混合膜,用拉曼光谱和红外光谱分析了碳膜的结构和键合方式,分析表明:碳膜中存在胺基团和氢原子.混合膜的荧光谱测量结果表明,认为正丁胺对染料荧光谱的影响是因为胺基和氢原子的存在.     

Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet–Spengler reaction

An efficient tandem approach for the selective synthesis of 4,5-dihydroimidazo[1,5-a]quinoxalines 6a–g and imidazo[1,5-a]quinoxalines 7a–h by the reaction of 2-imidazolyl anilines 4a–c with aryl aldehydes 5a–k under mild reaction conditions is described. Introduction of electron releasing alkyl groups in substrates 4a–b was found to be instrumental for the success of the reaction.     

Understanding the Diels-Alder reactivity of 1,2-azaborine analogues

The Diels-Alder reactivity of 1,2-heteroborines (H₄C₄B(H)X, X?=?NH, PH, AsH; O, S, Se) has been computationally explored by means of Density Functional Theory (DFT) calculations. The influence of the HB?=?X fragment on the reactivity of the system has been quantitatively analyzed in detail by means of the so-called Activation Strain Model (ASM) of reactivity. It is found that the interaction between these species and the dienophile is significantly stronger than that computed for their all-carbon isoelectronic counterpart, benzene. In addition, the strain energy plays a key role in the observed reactivity trends. The role of the aromaticity strength of these heteroarenes on the reactivity is also assessed.