《高分子化学》教学中有机化学知识的有效利用探索

高分子化学和有机化学紧密相连,后者是学习前者的基础.在高分子化学教学中,有效利用有机化学知识解释聚合物的一些概念,将有助于学生更好的理解和掌握高分子化学知识.本文根据教学实践,介绍了几点利用有机化学知识帮助解释高分子化学中的概念或反应的实例,并对教材中存在的疑点提出了自己的看法.     

大类培养模式下非化学化工专业有机化学教学改革

针对非化学化工专业学生在学习有机化学时出现的"有机化学无用论、乏味论和繁难论"等现象,对有机化学课程教学的各个环节(包括绪论设置、新课导入、课堂教学内容编排、教学手段、考核方式)进行改革探索,旨在为"促进非化学化工专业有机化学教学改革,提高学生学习效率"提供相应的研究思路和方法.     

新课程背景下高中生具备的有机化学知识基础探析——基于高考选拔和大学课程学习的需要角度

高中化学新课程有机化学的内容分别设置在“化学2”必修模块和“有机化学基础”等选修模块中。2007年新课程化学高考大纲将“有机化学基础”定为选考模块,新课程高中生学习的有机化学知识与以往相比发生了哪些改变,能否满足他们在大学学习的要求,对此,作者从高中课程标准、高考大纲、中学化学教材和大学化学课程等几个方面对学生的有机化学知识基础进行了分析,并结合新课程实施的具体情况初步论证了高中化学新课程中学生获得的有机化学知识基础与高考选拔和大学课程学习需要之间的适切性。     

《高分子化学》聚合机理教学中有机化学知识的衔接利用

高分子化学是在有机化学基础上发展而成一门学科,高分子的合成反应与有机小分子的合成反应密切相关,特别是高分子合成反应机理的学习中大量应用到有机化学的基础知识.因此,在高分子化学教学中有效利用有机化学知识是帮助学生更好理解和掌握高分子化学反应机理相关知识的关键.本文根据笔者教学实践,从烯类单体聚合活性及机理、自由基聚合阻聚机理、配位聚合机理等方面以实例形式探讨了如何利用有机化学知识帮助解释高分子化学中反应活性及反应机理.     

一种简易型混合式教学法在有机化学小班教学中的尝试

针对有机化学教学改革现状,利用现有网络教学资源及化学资料,将问题式教学法和翻转课堂教学理念融入传统教学方法中,构建了一种简易型混合式教学法,并应用于生物学专业拔尖学生试验班有机化学小班教学实践。结果表明,简易型混合式教学法能够培养学生学习兴趣,提高化学文献查阅、交流沟通、团队协作等综合能力,因而有助于提高有机化学的教学质量,促进拔尖人才的培养。     

有机化学基本知识在高分子化学中的应用

高分子化学与有机化学有着千丝万缕的联系,若能在高分子化学新知识点的授课中,及时引导学生回顾有机化学的相关知识点并加以阐述和拓展,强调有机化学和高分子化学的相互嫁接和相互渗透,不仅能使学生更加容易理解和接受新知识,提高学生的学习兴趣和活跃课堂气氛,而且可以起到温故而知新的教学效果。     

如何教学生正确地写出有机化合物的结构式

初次教有机化学这一部分时,由于对教材和大綱的钻研不够,以致对教材的系统性和重点、难点掌握不住,只能照着课文顺序讲下去。所以学生在学了有机化学后,对于正确写出有机化合物的结构式,特别感觉困难。由于学生没有抓住关键,所以在写结构式时,就乱拼乱凑,写得是否正确自己没有把握,结果造成许多错误。我针对这种情次进行了深入地分析,找出了在教学上存在的主要问题是: 1.我只是在有机化学的开始时,孤立地讲解了布特列洛夫的化学结构学说的内容,以后就没有把它应用于实际和贯徹到其他的章节中去。 2.对于各类有机化合物分子结构的特点没有重点突出。 3.对于容易混淆的部分没有进行对比。上述三个问题的产生主要是由于对大纲和教材的     

"同分异构体"错误概念的调查与分析

同分异构体是有机化学中的一个重要化学概念。通过问卷调查,发现学生头脑中存在着许多错误概念,而错误概念对学生学习有机化学产生严重的障碍。在教学中,教师应根据教学实际,及时纠正学生头脑中的错误概念,从而提高教学质量。     

非化学专业有机化学实验教学中对学生科研思维的培养

研究型大学对学生科研思维的培养至关重要,有机化学实验作为近化学专业类学生重要的基础实验课程,对学生操作技能、创新能力和科研思维培养有重要作用。本文以非化学专业本科生有机化学实验"大学化学实验(O)"的教学实践为例,从学生学习方式、教师教学方法、实验教学内容设置等方面阐述如何在教学过程中完成对学生科研思维的培养。     

有机化学知识在高分子化学教学中的应用

<高分子化学>是研究聚合反应机理和聚合方法的一门科学,是高分子材料专业的一门重要专业基础课,它与前期所学课程<有机化学>课程有着非常紧密的联系.有机化学知识在高分子化学中的应用有利于调动学生的学习积极性,加深对教学难点的理解,以便提高教学质量,达到更好的教学效果.本文结合高分子化学和有机化学的课堂教学实践,就有机化学知识在辅助高分子化学教学过程中的应用提出了一些实例和自己的体会.     

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.     

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.     

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.     

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%).