“课证赛”融合的分析化学实验教学新体系的构建与实践

经过几年来对分析化学实验教学的探索,建立了以基础分析化学实验教学为核心、开放性实验为拓展、研究性实验为延伸的培养模式,构建了"课证融合、课赛融合"的分析化学实验教学新模式。教学实践证明,该教学模式对化学类应用型人才培养具有一定的借鉴意义。     

新建应用型本科院校分析化学实验教学改革探讨

对分析化学实验教学内容、教学方式的现状进行了分析,并提出了改进措施;借鉴“翻转课堂”教学模式,以“不同品牌胃舒平药片中氢氧化铝和氧化镁含量的测定”为例,从课前教师准备学习资源、学生自主学习、师生课堂活动、课后交流和评价4个阶段设计并讨论“翻转课堂”模式在分析化学实验教学中初步实践。结果表明,“翻转课堂”教学模式能够有效避免传统分析化学实验教学中出现的“灌注式”“保姆式”实验教学模式;能够极大地激发学生学习和深入探究的热情。     

基于ADDIE模型的分析化学课程思政探索与实践

基于ADDIE模型建立分析、设计、开发、实施和评估一体化的分析化学课程思政模式。围绕“社会服务、科学发展、职业道德、哲学思辨”4条思政主线精选17个案例和8个哲学原理融入教学，构建了“课前点拨-课中内化-课后延伸”的长效思政育人方法。借助明尼苏达短式量表进行育人成效的评价。ADDIE课程思政模型的应用为分析化学教学提质增效，推动知能并进，实现对学生的价值引领。     

分析化学“设计性实验”教学的研究与实践

介绍了以培养学生的学习能力、解决问题的能力、交流能力、团队合作能力和创新能力为目标,集十年“设计性实验”教学的实践经验,确定了分析化学“设计性实验”的具体运行模式,利用自编讨论式实验教学电子课件、“设计性实验”教师参考资料库等开展实验教学.     

分析化学实验教学改革的几点建议

针对分析化学实验教学的现状,提出了分析化学实验教学改革的几点建议。改革实验教学内容,增加综合性和设计性实验;改革实验教学方法,弱化教师和课本的作用,增加学生的主动性;统筹安排实验课和理论课,力求2课进度基本一致;完善实验考核机制等,以培养适应社会需求的现代大学生。     

化学实验教学:冷与热的思考

对比初中化学评优课和常态课中实验教学的状况,分析化学实验在评优课中受热捧而日常教学遭冷遇的原因。依据2011年版义务教育化学课程标准中有关实验教学的规定和要求,提出从化学实验教学功能全面发挥的视角,提高对化学实验及其教学的认识,加强对化学实验教学的研究。建议从强化化学实验的功能意识、加强实验内容和功能的联系、注重实验教学行为的转变、重视学生良好实验习惯的养成等4个方面,提高化学实验教学质量。     

分析化学实验教学模式的优化与实践

以培养“服务型 创新型”人才为目的,从教学内容、教学方法和考核方式等方面对分析化学实验教学进行改革,建立了“基础型 设计型 创新型”实验教学模式,收到了良好的教学效果。     

以小型化分析化学实验启动实验教学模式的改革

小型化分析化学实验可将传统实验的教学时间由4学时缩短到2.5学时,以此为契机,开展“验证型、应用型、综合设计型”三阶段式实验教学新模式。     

虚拟仿真技术在大学分析化学实验教学中的应用*

针对传统分析化学实验教学中的不足,介绍了大学分析化学实验虚拟仿真线上教学项目的建设内容及其应用实效,并对虚拟仿真实验技术下一步的发展方向进行了设想。通过近2个学年的教学实践,发现以虚拟仿真实验辅助现场教学,可有效弥补传统分析化学实验教学中学生预习效果差、试剂废液产生量大、安全隐患频发等方面的缺陷;同时,虚拟仿真实验系统的考核评价、分析统计功能为教师在开展现场实验教学过程中,针对学生知识点掌握的薄弱环节开展针对性强化指导训练提供了有效手段。本虚拟仿真实验系统为虚拟仿真技术在大学分析化学实验教学领域的推广应用提供了有益借鉴。     

基于微课的翻转课堂教学模式在分析化学实验教学中的探索

分析化学实验是大学化学实验的重要内容,是分析化学课程学习中不可缺少的组成部分。为了提高分析化学实验教学质量,提升学生动手能力、分析问题和解决问题的能力以及创新能力,解决传统教学模式存在的主要问题,对分析化学实验教学模式进行了改革探索。将以微课为基础的翻转课堂教学模式引入到分析化学实验中,激发学生的实验热情,提高学生综合实验技能,巩固基础理论知识,培养了科学研究思维,真正实现创新性人才培养目标。     

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.     

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.     

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.     

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.     

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.     

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.     

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.