以能力为导向的近化学类专业实验教学体系建设与实践

以提高学生能力为导向,对近化学类专业实验教学体系进行改革与实践.以“教-学-研”一体化建设为主线、虚拟实验室和开放实验室的建设为抓手、课内外教学结合为手段,分层次、多模块构建了“一主线、两结合、三层次”的实验教学体系.突出理论应用、技能训练与创新能力培养,对实验教学进行教学模式与教学方法改革探索,丰富了实验内容和组织形式,将专业知识、实践技能、综合素养的训练有机结合,更好地体现了重基础、强应用的人才培养目标,初步建立了具有鲜明人才培养特色的实验教学体系.     

农科基础化学实验研究性教学模式的构建与实践

针对农林高校化学实验教学中存在的问题, 提出以培养学生自主学习和创新能力为教学目标, 通过优化教学内容、改革教学方法, 提高学生学习兴趣, 形成了基础实验、综合设计性实验、研究性实验和创新实验等多层次实验教学体系, 构建了农科基础化学实验研究性教学模式。这对于提高学生的学习效率, 培养学生的自主学习能力与创新能力具有重要意义。     

基于PBL模式的化学实验设计与实施——以光催化降解染料脱色实验为例

以染料废水的降解脱色实验为例,探讨了PBL模式在化学实验教学中的应用,提出了基于PBL模式的化学实验教学运行程序及教学评价。在实验教学中,基于PBL的模式,以解决问题为任务驱动,发挥问题对学习过程的指导作用,鼓励学生积极参与教学过程,调动了学生学习的主动性和积极性,提高了学生掌握知识并应用于实践的能力,培养了学生的创造精神和创新能力。     

基于云班课的物理化学开放性实验教学实践*

以云班课为教学平台,采用翻转课堂为主的教学模式开展物理化学开放性实验教学,详细介绍了开放性实验分层教学体系、实验教学内容、微课的设计方法和实践过程。实践结果表明,通过这些教学手段,教师能顺利地开展开放性实验教学,提升学生的学习兴趣和创新能力,同时也提高了实验室资源的利用率。     

“以学生为中心”的高分子化学实验教学改革与探索

高分子化学实验是高分子材料与工程专业本科生的专业必修课程,是培养学生实践能力和创新能力的关键环节。针对高分子化学实验教学过程中存在的问题,从“以学生为中心”的教学理念出发,围绕优化实验教学内容、革新实验教学方法、健全实验评价制度等进行改革,从而锻炼和培养学生的创新能力和解决复杂工程问题的实践能力,全面提升学生的综合素质,满足社会对高素质综合型人才的需求。     

有机化学实验教学资源的建设与实践

教学资源建设是高校教学改革的一项重要工作。以提高实验教学质量和培养创新能力为目标,探索了我校有机化学实验教学资源的建设内容,并通过网络平台用于辅助教学。视频资源,有效地提高了课前预习效果;课件资源,培养了学生的实验设计思想和创新能力;拓展资源,开拓了学生的视野,提高了化学实验兴趣;在线测试题库资源,有效准确地检验了学生的理论水平。教学资源通过实践应用,教学效果明显,切实提高了教学质量。     

在实验教学中培养创新能力的尝试

在实验教学中通过开放式教学、研究式学习,探索新问题、设计新实验,以激发学生的学习兴趣,培养创新能力。     

分析化学实验教学改革探索

针对分析化学实验教学中教学内容设置不当,教学模式"保姆式",教学方法单一等问题,通过改变教学理念、构建新型实验教学体系以及改革实验教学方法等多种措施,提升了学生的实验兴趣,培养了学生的工作责任心和探索精神,提高了学生的应用创新能力。     

基于“学习金字塔理论”的物理化学实验教学模式改革实践

介绍了东北林业大学物理化学实验课程教学中基于"学习金字塔理论"进行教学模式改革实践的情况。在实施实验教学过程中,通过增加"学生通过在线实验视频预习""学生为学生讲解实验""操作前学生小组讨论"和"操作后学生小组总结讨论"等学习环节,建立了一种有效的"以学生为中心"的实验教学模式,促进了学生综合素质和创新能力的培养,取得了良好的教学效果。     

高师“化学教学论实验”教学变革研究

基于师范生专业能力提升和"化学教学论实验"教学存在对学生实验研究能力、创新能力和教学能力培养不足的现状,实施教学变革研究。通过开展以疑难实验为主题的研究性设计和实验教学活动,提升学生教学研究意识和能力,并在实践中全面提升师范生专业能力。     

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.     

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%).     

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.     

Synthesis of N-substituted carbazolones from α-iodo enaminones via Pd(0)-catalyzed intramolecular coupling under microwave irradiation

A variety of N-aryl and N-alkyl carbazolones were conveniently achieved in good to high yields via Pd₂(dba)₃-mediated intramolecular coupling of N-substituted α-iodo enaminones under microwave irradiation. The Pd(0)-catalyzed cyclization was found to proceed favorably with the more electron-deficient phenyl ring during the reactions involving unsymmetrical N,N-diaryl α-iodo enaminones. This unique property enables the construction of carbazolone skeleton containing nitro substituted benzenoid ring.     

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.     

Synthesis of substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles by intramolecular nitrilimine cycloaddition

Both substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles have been synthesized by the 3+2 intramolecular dipolar cycloaddition of nitrilimines to alkynes. This cyclization has been extended to more versatile 3-bromo derivatives by the use of alkynylbromides as dipolarophiles.