中国优秀传统文化融入STEAM实践的教学——沉淀溶解平衡

基于STEAM理论，以中国山水画的传统艺术为教学情境，以沉淀溶解平衡知识为载体，以化学试剂为色彩将优秀传统文化融入化学学科教学设计，引导学生在获取知识的过程中提高人文素养，增强文化自信。     

化学专业英语教学中工具性与人文性的统一*——基于母语的正迁移

以化学专业英语为载体,通过母语在词汇词源、共有性专业知识及学科核心素养之科学精神中的正迁移,在教学过程中提升大学生对中华民族传统文化的认知与共情,弘扬优秀文化价值观、树立文化自信,实现知识传授、能力培养和价值引领的有机融合,促进学科专业性语言工具性与人文性的统一。     

人物传记类化学科普图书的育人功能研究*——基于《呦呦寻蒿记》的案例分析

科普图书是落实“立德树人”根本任务的重要载体。以《呦呦寻蒿记》为案例,挖掘人物传记类化学科普图书的育人功能,发现此类图书具有树立理想信念、厚植爱国情怀、提升文化自信、形成生态文明意识的德育功能;具有普及化学基础知识、倡导化学思维方法、提升科学探究能力的智育功能;具有树立增强体质观念、调节心理健康发展的体育功能;具有提升感知美审美品质、创造美创新素养的美育功能;具有认同敬业乐业观念、提升高效劳动技能、培养实干兴邦精神的劳育功能。为落实“五育融合”育人功能,必须加强内容创作专业化、政策支持常态化、图书管理制度化、图书价值外显化。     

文教融合，以学促保——以非物质文化遗产的保护传承在化学与社会课程中的呈现为例

非物质文化遗产是我国文化软实力“活”的呈现,为华夏璀璨文化提供根基和养分。本文以我国非物质文化遗产中所蕴藏的化学智慧为线索,让化学、科技、文化在化学类通识课程中相互融合碰撞,让课堂充满知识性与趣味性。论文通过文教融合,实现非物质文化遗产的保护传承,进一步助推非物质文化遗产文化现代化,在保护传承中创新,增强学生对非物质文化遗产的科技和文化自信,最终达到以学促保的目的。     

化学通识课程“人文化学”中的文化自信培养——中国陶瓷的魅力

通识教育是引领广大学子形成完整的知识架构,走向智与美兼具的人生的重要课程。本文以笔者所开设的化学类通识课程“人文化学”中讨论中国陶瓷的部分为例,介绍了中国陶瓷发展的几个重要阶段的艺术特色及其背后的化学基础,探索了如何在通识教育中将科学知识与文化底蕴有机结合,激励学生增强民族文化自信,培养学生提高科学和人文素养。     

建构学习仪式感 提升学习主动性*——以元素化学学习为例

结合元素化学课程特色和当代大学生心理性格特征,提出以学生为主体、提升学生素养能力为重点,构建元素代言人、身边的化学(现象、实验)、翻转课堂等一系列课内外学习活动,以学习活动的仪式感促进学生进行自我暗示,塑造愉悦学习的情境,克服焦虑厌学的情绪,提升学生学习的主动性,并以学科育人的思想贯穿课程始终,营造有形有实、充满活力的元素化学课堂。     

传统文化蕴含的化学智慧在元素无机化学教学中的有机融入

在讲授元素无机化学时,把中国传统文化中所包含的化学知识、化学智慧有机地融入课堂教学,将元素无机化学讲授与课程思政教学有机融合,从而增加理科课堂的文化性、知识性和趣味性,激发学生的学习兴趣;同时培养学生的文化自信,激发学生的民族自豪感。     

课程思政视角下化学思维型课堂的建构*——以“乙醇”的教学为例

通过以真实问题为情境,以化学知识结构化与化学核心观念为基础,以问题的探究为路径,以乙醇教学为例,建构了课程思政视角下的化学思维型课堂即“两思课堂”的基本教学模型,探索了“两思课堂”的评价方法与内容。通过分析学生表现可知两思课堂能同步实现核心价值培育与化学学科核心素养培养,有效实现化学学科的育人价值。     

化学学科核心素养为本的高三化学深度复习*——以沉淀滴定为例

以沉淀滴定为例阐述在高三教学中进行化学学科核心素养为本的高三化学深度复习。分析了教学背景和复习目标,详细呈现了教学过程,并对教学效果进行了检测和反思。素养为本的高三化学深度复习关键是:创设真实情境,激发学习欲望;解决真实的问题,发展高阶思维;教、学、评一体化,促进素养提升。     

“绿色化学”的项目式教学*——环氧乙烷制备工艺中的绿色化学

以“环氧乙烷制备工艺中的绿色化学”为项目式学习主题,以绿色化学概念学习、化学工艺中绿色化学的设计评价等为项目学习活动,探究绿色化学理念的教学设计。培养学生绿色化学意识,提升科学态度和社会责任的化学学科核心素养。     

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.     

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.     

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.     

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.     

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.     

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.