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。     

深度学习视域下“线上线下”混合式教学模式应用实践*——以“无机与分析化学”课程为例

深度学习视域下“线上线下”混合式教学模式的核心是学生的深度参与、高级学习策略的使用及教师的优质讲授,最终实现学生深度学习能力的养成。“无机与分析化学”线上线下混合式教学通过在线预习、课堂讨论、课前课后测试、实践教学等多种教学设计,让学生化“被动”学习为“主动”学习,深度参与,锻炼学生自主学习能力,增强学生团队协作及解决复杂工程问题的能力,启发学生创新应用能力。     

转动课堂在分析化学教学中的应用

"转动课堂"是渤海大学依据地方综合性大学的人才培养目标,借鉴国内外的课堂教学模式引申而来,将课堂精讲与师生互动紧密结合,个性化培养学生的创新能力和动手能力。本文介绍了分析化学结合学科特点及转动课堂核心理念,设计自学、精讲、互动等8个教学环节以提高课堂效率。这种课内课外协同互补的教学模式,激发了学生学习分析化学课程的热情,课堂教学质量及学生学习效果明显提高。     

专题研讨课教学法在分析化学课程中的实践

以2012、2013和2014级药学专业学生为研究对象,在分析化学课程教学中开设“分析测试的质量保证”专题研讨课。通过课堂汇报、问卷调查和研讨总结及体会报告的方式对教学效果进行评价。结果表明,该教学法有利于培养学生的逻辑思维能力,自主学习能力,以及发现问题、分析问题和解决问题等多方面的能力,起到了提高教学质量的效果。     

混合式教学法在分析化学教学中的设计与实践*——以“碘量法”为例

针对中医药类专业中分析化学课堂以教为主、师生互动少、教学效果较差等问题,借鉴“线上线下(O2O)”混合教学模式,利用清华在线网络平台、雨课堂和中国MOOC等网络资源开展课程建设,并对分析化学课堂教学进行改革,重构教学理念和教学流程,“翻转”师生角色,将线上与线下教学有机统一,借助线上的网络学习资源、测试平台等帮助学生在时间和空间上自由学习,达到学生个性化、差异化学习的目的。     

面向高阶思维培养的自主型实验教学模式的设计与实践*

基于教育现代化、发展“互联网+教育”、培养创新性人才的指导思想,结合“超星学习通”网络平台与实验课堂的优势,设计了面向高阶思维培养的“预习自测-讲授讨论-自主实践-总结反思”的四段自主型实验教学模式,并应用于化学与化工类专业分析化学实验课程的教学实践。该实验教学模式增加了学生自主学习时间,培养了学生“分析、综合、评价和创造”等高阶思维能力,提高了实验课程的教学效率,为高等院校实践实验教学的改革提供了参考依据。     

探究式教学模式在分析化学综合实验教学中的实践

介绍了中国科学技术大学分析化学实验教学模式的探索和实践。在掌握基本的定量分析操作的基础上,如何提升学生自主探究实验的能力及自主设计实验的高阶创新实验能力是分析化学实验需要达成的教学目标。探究学习是一种以学生基于问题而展开的学习方式,教学中我们采用这样的教学模式能充分调动学生学习的积极性,通过实施这样的教学模式,学生在探究中不断提升了发现问题、分析问题、解决问题的能力,从而达到培养学生创新能力的目的。     

建构主义教学理论在无机及分析化学教学中的探索与实践

在无机及分析化学的教学实践中，探讨了怎样结合无机及分析化学课程的特点运用建构主义教学理论。根据课程内容采取相应的教学模式，培养学生的自主学习能力，进一步提高教学质量，并促进创新人才的培养。     

雨课堂在分析化学教学中的应用

分析化学是一门理论性和应用性都很强的基础学科，为了进一步提高学生的学习兴趣，培养学生分析问题和解决问题的能力，加强师生之间的互动，尝试把雨课堂的线上线下教学模式应用到课程教学过程中。实践证明，运用雨课堂教学，学生学习的积极性和考试成绩都得到了明显的改善，极大程度上推动了分析化学教学改革的发展。     

基于STEM教学理念的分析化学实验教学新模式探索——以“自来水硬度测定”为例

STEM是一种集科学、技术、工程、数学多学科融合的项目式教育理念,旨在通过融合多学科知识完成项目目标,从而培养学生提出问题、分析问题以及解决问题的能力,进而激发学生的科学探索精神和创新思维能力,已经成为当前国际教育研究和改革的热点。本文将STEM教育理念引入分析化学实验教学过程中,探索发展分析化学实验课程教学新模式。倡导以学生为中心、以真实问题为牵引,学生以相关课程理论为线索,自主完成实验方案设计、实验过程、实验结果分析等一系列分析化学实验过程,从而培养学生的科学探索与实践能力。主要从课程内容、教学方法以及考核方式等三个方面来探索分析化学实验教学新模式,进而提高分析化学实验的教学质量和学生的学习兴趣和科学素养。     

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%.     

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.     

A general and convenient synthesis of 4-(tosylmethyl)semicarbazones and their use in amidoalkylation of hydrogen,heteroatom, and carbon nucleophiles

A general synthesis of previously unknown semicarbazone-based α-amidoalkylating reagents, 4-(tosylmethyl)semicarbazones, has been developed. The synthesis involved three-component condensation of semicarbazones of aliphatic or aromatic aldehydes with the same or other aldehydes and p-toluenesulfinic acid. The scope and limitations of this reaction were investigated. The compounds obtained were demonstrated to be an efficient α-(4-semicarbazono)alkylating agents. They were reacted with H- (sodium borohydride), O- (sodium methylate), S- (sodium phenylthiolate), N- (pyrrolidine, sodium succinimide), P- (trialkyl phosphites), and C-nucleophiles (sodium diethyl malonate) to give the corresponding products of the tosyl group substitution, 4-substituted semicarbazones, including analogues of nitrofurazone. Among the prepared compounds tested in vitro for antibacterial and antifungal activity, three nitrofuryl-containing semicarbazones exhibited high biological activities with minimum inhibitory concentration (MIC) values of 8–32 μg/mL.     

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.     

Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde

A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki–Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.     

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.     

Microwave-assisted copper-catalyzed stereoselective ring expansion of three-membered heterocycles with α-diazo-β-dicarbonyl compounds

Microwave-assisted copper-catalyzed ring expansions of three-membered heterocycles with α-diazo-β-dicarbonyl compounds were investigated. Thiiranes generated 3-acyl-5,6-dihydro-1,4-oxathiines in the presence of copper sulfate and trans-3-acyl-5,6-dihydro-1,4-oxathiines as stereospecific products for 1,2-disubstituted cis-thiiranes through an intramolecular S_N2 process. Oxiranes gave rise to 2-acyl-5,6-dihydro-1,4-dioxines under the catalysis of copper hexafluoroacetylacetonate and cis-3-acyl-5,6-dihydro-1,4-dioxines as stereospecific products for 1,2-disubstituted cis-oxiranes via an intimate ion-pair mechanism. The current method provides a direct and simple strategy in efficient preparation of 3-acyl-5,6-dihydro-1,4-oxathiines and 2-acyl-5,6-dihydro-1,4-dioxines, important agents in medicinal and agricultural chemistry, from readily available thiiranes and oxiranes, respectively.     

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.