药物化学课程思政教学模式的探索与实践*——青霉素抗生素专题

药物化学是药学专业核心课程,拥有丰富的思政资源。以药物化学课程为研究对象,在明确课程思政育人目标基础上,将药物化学课程思政教学主线设置为“定目标、拆内容、寻热点、挖元素、隐融入、明效果、做评价”等7个环节。进一步以青霉素专题为例,展示思政内容有机融入课程教学的全过程,为其他理工类专业课程思政教学提供一种参考模式。     

化学专业概论教学中的课程思政探索与实践*——以华中科技大学“一院一品”化学专业概论课为例

课程思政是高校落实立德树人根本任务的重要举措,是完善“三全育人”的重要抓手。化学是我国科学研究的重要基础,对提升原始创新能力具有重要意义。化学专业教学中融入思想政治教育的前提是建设好一门课程。针对当前专业课教学中存在的课程思政体系不完善、思政元素与专业课程融合程度低、教师思政教学水平有待提高等问题,以华中科技大学化学与化工学院专业概论课为试点,完善课程设计与教学方法,探索化学专业教学中的课程思政建设。通过剖析化学课程思政的意义与难点,构建专业概论课实施方案,形成一套行之有效的化学课程思政建设体系。     

基于雨课堂和BOPPPS改进模型的教学设计——以大学化学课程为例

在高等学校专业课程教学中融入思政教育教学的理念,是以"立德树人"为教育根本任务的基本要求。结合结构化学课程特点和教学内容,以"培养学生的哲学观和科学观、培养学生民族自豪感和自信心"的目标为切入点,提出结构化学教学中思政元素的融入策略,发挥结构化学课程的"育德功能",实现知识传授和价值引领的有机统一。     

化学课程与教学论课程思政实践

课程思政是化学课程与教学论课程落实立德树人的重要内容之一。基于化学课程与教学论课程理论性、实践性、师范性强等特点,从设计课程目标、挖掘课程思政元素、建设课程思政教学案例库、提升教师课程思政能力等4个方面探索了课程思政的实践,从学生评价、课程成绩考核等2个方面探究了课程思政的教学成果评价。以期为化学(师范)专业的课程思政体系建设提供参考。     

化学类专业课程思政要素与途径的探索和实践

探讨了化学类专业课程思政要素、教学方法和途径,提出了“六维度、四构建”思政教学策略。从化学中的哲学思想、化学的价值观、化学科学精神、化学思维方法、化学伦理、化学文化“六维度”确定化学类专业课程思政要素;以教学目标创建为基础、教学内容和教学资源重构为重点、教学方法构建为关键、成绩评定体系建立为保障的“四构建”系统设计课程思政的教学方法和途径。基于“六维度、四构建”课程思政策略,对无机及分析化学课程进行了教学实践。实施结果表明,这些策略能有效提高课程育人的针对性和有效性,为高校同类课程思政建设提供一个可借鉴的思路和模式。     

环境化学课程思政内涵建设与实践*

环境化学课程对于提高学生的环境污染认识水平和污染治理实践能力发挥重要作用。重构了基于课程思政的“三位一体”课程目标;针对环境化学课程内容特色,从培养正确环境观和环境污染观,建立正确分析和解决问题的科学素养,形成良好环保习惯等角度深入挖掘课程思政点,建立了思政元素与人才德育培养目标的融合体系;基于思政元素滴灌渗透,构建了立体化教学育人模式。实践成效分析表明,基于课程思政特征显著的教学设计,能够实现课程思政内涵在环境化学教学中的有机融合与精准对接,学生主体的翻转课堂促进了能力提升与价值塑造的同频共振,学生的学习获得感和素养能力都有较大提高,达到“素养+能力+知识”一体化课程学习目标。其中,教师科研反哺教学更能触发学生的学习热情和拓展实践意愿。因此,在课程思政育人中要充分重视身边教师对学生潜移默化的榜样效应。     

高职专业课的课程思政教学探索与实践——以“配位化合物”的思政教学为例

以医学专业医用化学课程的重难点内容“配位化合物”的思政为例,从教学实施、教学评价及教学反馈等3个方面探讨了高职院校专业课程的思政教学,以期为高职院校开展以课程思政为理念的课堂教学改革提供借鉴。     

化学分析课程思政具体案例设计及思考

如何在化学核心课中融入课程思政元素,形成协同育人效应,是当前课程建设的一项重要任务。本文介绍了湖南大学分析化学教学团队在化学分析课程中的课程思政案例设计经验与思考,围绕化学分析各部分的教学特点,构建相应的教学案例,体现课程设计的教学目标和思政育人目标,同时提出具有普适性的课程思政设计理念。     

元素化学课程思政案例库建设及线上线下混合递进式教学实践

教学团队立足元素化学课程特点,设计、建设了“科学”“人文”“思政”三融合的元素化学课程思政案例库,并将之融入线上线下混合递进式教学的各个阶段和环节,以同步实现知识传授、能力培养、价值塑造三位一体的教学目标。同时,建立课程思政的集体教研制度,确保课程思政的整体性和持续性。     

无机化学课程思政探索——以“配位化学基础”中部分内容的教学设计为例

课程思政是将思想政治教育元素融入课程教学,深化专业课程教书育人的内涵。在教学过程中,以基础理论知识为主线,融入化学发展史、化学家的主要贡献、化学学科和生产生活的紧密联系以及当代科技研究前沿等内容,构建无机化学课程思政教学体系。本文以配位化学基础中部分内容的教学设计为例,对思政案例进行介绍。     

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.