Teaching System Construction of Polymer Chemistry Experiment and its Function on Training Creative Applying Talents

高分子化学是材料化学专业重要的技术基础课,是一门以实验为基础的学科,因此,高分子化学实验是高分子科研和高分子教学的重要组成部分,是学生在掌握高分子化学的基础上,学习高分子合成的各种实验技术、聚合实施方法,培养学生进行高分子材料研究和技术开发的基本能力。从市场就业对高分子材料方向的人才需求出发,以培养创新性应用型人才为目标,通过开展实验技术讲座、改进基础性实验为综合性实验和设计性实验、增加研究性实验对高分子化学实验教学体系进行了改革,实验内容体现材料的应用性和工程价值,培养了学生的创新能力、工程实践能力。     

从高分子化学的一个趣味实验谈如何培养学生的综合实验能力

高分子化学是一门实验性很强的学科,是高分子材料合成、加工和应用的基础,也是高分子专业研究生入学考试必考的科目之一,但如何提高学生们的实验观察能力和动手操作能力成为近些年来各高校培养学生的重点课题。而在高分子化学实验合成方法中,悬浮聚合方法由于反应温度低、操作方便、反应过程容易散热、聚合物粒度容易控制、水为分散介质廉价等优点,在橡胶、塑料等高分子材料合成工艺中被广泛应用。本文以高分子化学悬浮聚合实验为例,从"看"、"听"、"摸"、"嗅"多个角度向学生们展示了高分子化学反应在不同反应条件下及不同反应阶段所表现出的实验现象及反应结果,旨在提高学生们的综合实验能力,使之早日踏上科研探索之路。     

DOPA-PSPMA仿生共聚物综合探究性实验研究

为提高本科学生的创新创业能力,通过高分子化学实验教学使学生深入了解仿生共聚物的制备及性能的相关知识,设计了综合探究性实验。通过原子转移自由基聚合法制备仿生共聚物,并将其修饰在多种材料表面。采用X射线光电子能谱、扫描电子显微镜、生物显微镜分别对修饰材料进行表征。该实验通过共聚物的制备使学生掌握高分子化学中活性可控自由基聚合制备共聚物的方法;掌握仿生共聚物设计及构筑方法;使学生学习科研仪器的操作方法,切实提高学生的实践能力。该实验重复性好、创新性及拓展性强,将共聚物设计制备及应用有机结合,适用于高分子专业本科生综合探究性实验。     

太阳光用于可逆加成-断裂链转移（RAFT）聚合反应的实验设计

作为培养应用型人才目标的新尝试,从研究性教学的理念出发,设计了太阳光诱导可逆加成-断裂链转移（RAFT）聚合的综合性高分子化学实验教学项目。该实验应用太阳光辐照,在仅添加S-十二烷基-S'-（α,α″-甲基-α″-乙酸）三硫代碳酸酯的情况下,进行了2-乙烯基吡啶的RAFT聚合实验。实验巧妙地将太阳光应用在RAFT聚合实验中,该实验具有实验现象明显和操作简单易行的优点。     

高分子实验教学改革的几点探索

高分子实验课程是高分子化学和高分子物理课程教学的一种有效的实践教学形式,通过这一环节的学习和实践,可以使学生进一步巩固高分子的基本概念和理论。本文介绍了在高分子实验教学中的几点探索性改革措施,在开设原有验证性实验的基础上,增设了设计性和综合性实验。设计性实验的特点是实验方案的灵活多样;综合性实验则偏重高分子化学和高分子物理两门课程知识点的结合。实践证明,这些改革可有效激发学生的学习兴趣,提高学生的动手能力和创新意识,是培养学生综合素质的重要途径。     

高师院校化学（教育）专业实验内容改革探索与实践

分析了高师院校化学（教育）专业实验课程（又称化学教学论实验课程）的教学目标和教学现状,结合教学实际提出了高师院校化学（教育）专业实验课程的内容改革方案：（1）重视基础实验,强化训练实验技能;（2）增加探究实验,培养实验探究能力;（3）加强设计实验,着力培养实验教学能力;（4）拓展课程内容,提高实验创新能力。根据这些实验课程内容改革方案,并进行了相应的教学实践。     

苯乙烯阴离子聚合仿真实验软件的研究

烯类单体的阴离子聚合是高分子化学课程中主要理论内容之一,为了使学生更好地掌握和运用理论知识,通常需要配合实验教学加以验证。而传统的烯类单体的阴离子聚合实验由于受各方面条件限制,实验效果欠佳。本文以苯乙烯阴离子聚合实验的开展为背景,介绍了聚合实验软件平台的设计、开发、硬件系统和实验的内容。经过验证,该实验软件平台功能完善,界面简洁,运行稳定,可以结合实际硬件设备以及具体需求进行实验教学。     

绿色化学理念在高分子化学实验教学中的渗透

绿色化学是促进人类与自然和谐发展的化学,培养绿色化学意识是实现社会可持续发展的基本要求。高分子化学实验是高等院校高分子材料专业或材料化学高分子方向本科生开设的一门必修课,对学生进行绿色化学教育具有非常有利的条件。文章分析了在高分子化学实验课程中开展绿色化学教育的必要性与可行性;介绍了高分子化学实验教学中开展绿色化学教育的具体措施。通过绿色化学理念在高分子化学实验教学中渗透,在提高学生动手能力的同时,又增强了学生的绿色化学意识。     

高分子化学实验教学的初步探索

主要从四个方面介绍了我校在高分子化学实验教学过程中所做的初步探索:第一,加强实验教学环节,对验证性实验进行改进,设法提高学生对于实验的兴趣和实验教学效果;第二,改革传统的高分子化学实验教学的模式和教学内容,将高分子化学、高分子物理和成型加工所学知识有机结合起来,开设综合性高分子实验课程;第三,紧密结合本校教师科研情况,开设研究创新性实验,并开设第二课程,鼓励学生利用课余时间参与教师的科研,以培养学生独立分析问题、解决问题的能力;第四,结合本校实际情况,适量开设微量、半微量实验。     

固体核磁共振定量表征方法及其在高分子结构研究中的应用

高分子材料拥有众多优良的特性,使其广泛应用于现代社会的生产、生活及高新科技等领域。对于高分子特性的研究离不开微观物理、化学结构的定量表征。在众多表征高分子结构定量信息的实验技术中,固体核磁共振（SSNMR）发挥着重要的作用。它可以定量表征高分子的化学结构、材料体系的相成分及共混组分等,从而实现了难溶高分子产物的结构鉴定,以及高分子微观物理、化学结构关联材料性能的研究。然而,传统的SSNMR定量方法（直接激发法,DD）往往需要耗费十几个小时甚至数天的实验时间。交叉极化方法（CP）虽然大大缩短了实验时间,却往往无法提供定量的信息。基于此,研究者们提出了多个定量CP的实验方法,同时满足了方法定量性和实验耗时短的需求。本文综述了传统SSNMR定量方法及几种定量的CP方法,简单介绍了每个方法的基本原理,并平行阐述了实验方法的应用范围及特点,通过部分实例展示了SSNMR定量方法在高分子材料领域的应用价值,为研究者研发新型的高分子材料提供可靠并有效的结构表征手段。     

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.     

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.     

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.     

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.     

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.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

Regiospecific and direct imidation of the methyl C(sp³)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.     

Selective syntheses of 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones via temperature-dependent Rh(II)-carbenoid-mediated 2H-azirine-ring expansion

The Rh(II)-catalyzed reaction of 2-carbonyl-substituted 2H-azirines with ethyl 2-cyano-2-diazoacetate or 2-diazo-3,3,3-trifluoropropionate provides an easy access to 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones. These compounds can be selectively prepared from the same starting material using temperature as the only varied parameter. The 2-azabuta-1,3-diene intermediate, a common precursor for both heterocyclic products, isomerizes into 2H-1,3-oxazine under kinetic control, while 1H-pyrrol-3(2H)-one is the sole product of the reaction at elevated temperatures. According to DFT-calculations a one-atom oxazine ring contraction involving ring-opening to a 2-azabuta-1,3-diene intermediate, followed by a 1,5- and 1,2-prototropic shift leads to the consecutive formation of imidoylketene and azomethine ylide, which then further undergo cyclization to the pyrrole derivative.     

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.