能“锗”多劳

锗自“诞生之日”起就是一种明星元素，它的发现填补了元素周期表的空白，巩固了元素周期律的地位；锗晶体具有一系列优良特性，在半导体、红外光学器件、纤维光学器件与通信工业中应用广泛，是重要的国防战略储备；近年来，锗元素具有的独特理化性质及其生物效应逐渐为人们所认识，俨然成为了医疗保健领域的“明星元素”。然而，其生物效应的发生机理仍待解析，需要进一步的系统研究与论证。     

以“位构性”模型建构和学科能力发展的必修“原子结构 元素周期律”教学设计和实践*

在高中必修阶段“原子结构 元素周期律”主题已有研究的基础上,将“位构性”系统模型与学科能力活动任务相结合,提出了本研究的理论框架,进行了单元整体的教学设计并实施。通过预设学生的表现水平,设计各课时的评价任务,过程性地诊断学生在各个课时中“位构性”模型建构与学科能力的发展水平,描述学生在本章学习过程中的发展变化,促进了学生“证据推理与模型认知”等核心素养的发展。最后,归纳出以“位构性”模型建构和学科能力发展的“原子结构 元素周期律”在教学实践中的有效策略。以期能够对日后开展“原子结构 元素周期律”主题的教学设计与实践能够提供参考和建议。     

高中生“绿色应用”素养的测评研究

基于绿色化学对社会可持续发展的重要性,提出科学教育中“绿色应用”素养的理论框架,结合高中生化学学习特征开发测评工具,实施测量,分析处理测试数据,探查了高中生“绿色应用”素养的行为水平。研究发现,高中生“绿色应用”素养水平与其学科能力水平具有较好的一致性,不存在性别差异。测评结果为绿色化学实践提供借鉴和启发,以促进学生“绿色应用”素养的提升。     

基于核心素养的HPS教学实践——以“甲烷”为例

基于化学核心素养,以“打开第二自然界的大门”开启甲烷的科学探究与体验之旅,在“历史线”“活动线”“知识线”等3条认知与体验路线中,经历科学概念的形成过程,实现对“稻草变黄金”科学本质的理解,有效地将HPS教育与化学核心素养结合起来,使学生体会化学发展的过程与方法,感受化学的学科魅力和发展成就,以提高学生的学习兴趣。     

布卢姆教育目标分类视角下的中美化学教材习题比较——以“氧化还原反应和电化学”为例

基于布卢姆教育目标分类学,从知识、认知过程2个评价维度对中美化学教材“氧化还原反应和电化学”主题的习题进行了比较研究,结果表明,在知识维度,2国教材均较为重视“概念性知识”和“程序性知识”,但中国教材侧重前者而美国教材侧重后者;在认知过程维度,美国教材对“理解”“运用”水平的考查均较多且尤为侧重“运用”,中国教材对“运用”“理解”“分析”水平的考查均较多,整体上较为均衡。教材习题编写应该关注习题的课程功能创生,注重对学生学科思维、解决实际问题能力的考查,充分发挥其对教与学尤其是学生学习方式的引导作用。     

化学实验“三三三”翻转教学模式的探索与实践*

针对当前化学实验翻转课堂教学模式中存在的不足,依托“云班课”,重构了以学生为中心的化学实验“三三三”翻转教学新模式,即将实验教学划分为“三个课堂”:自学课堂、理论课堂和实验课堂等;理论课堂里包含“三个环节”:个人汇报、小组活动和测试点评等;学习效果评判有“三个评价”:自学评价、参与评价和动手评价等。以有机化学实验中“环己烯的合成”为例,采用该新的教学模式开展了教学活动,整个教学过程不仅体现了“以学定教、学生为中心”的教学理念,而且也能发挥出线下传统课堂的优势,实现了将“知识内化”的时间拉长,达到对学生线上自学“知识传授”掌握度的有力检验的目的,更有时间和空间进行课程思政元素的挖掘与融入,完成在知识传播中实现对学生的价值引领。     

促进学生化学学科核心素养发展的“铁盐和亚铁盐”的单元教学

设计了“铁盐和亚铁盐”的单元教学,以“探究硫酸亚铁的性质”和“线路板腐蚀液的研究”为核心任务,把铁盐与亚铁盐的性质、Fe²⁺和Fe³⁺的相互转化等核心知识贯穿其中,建立从物质类别、元素价态视角研究物质性质及转化的思路方法,促进多维度化学学科核心素养的融合发展。经过多轮次教学改进,结合教学实践过程及其教学效果抽提出“注重应用无机物的认识模型,重点把握研究物质性质的角度和思路”“抓住典型活动,培养学生的关键能力”“设计开放性任务,通过有效的师生对话进行诊断,外显问题解决思路”等教学策略。     

高中生对“物质的量”概念群的理解水平测查

通过编制信度、效度可靠的测量工具对高中生“物质的量”概念群的理解水平进行测查,发现大部分学生主要处于部分理解并伴随一定的误解的理解水平;学生对各概念的理解均存在迷思概念;学生在“物质的量”概念群中的迷思概念共计14条。     

化学师范生教学设计的评价研究*——以广州市某高校为例

利用化学教学设计评价量表(CTDES),对广州市某高校86名化学师范生在教育实习期间完成的教学设计进行评价,发现师范生在“认知与元认知”“社会文化与情感”“科学描述与应用”指标表现中等,在“一致性”指标表现较好。师范生在对“理论化学”和“描述化学”类课题进行教学设计时,在“认知与元认知”“社会文化与情感”“科学描述与应用”3个指标上的得分存在显著差异。     

高中化学“铁及其化合物”的项目式教学*——探秘铁肥的合理使用

以“探秘铁肥的合理使用”为主题,开展高中化学“铁及其化合物”的项目式教学。通过完成“确定铁肥的主要成分”“检验铁肥是否变质”“铁肥的合理使用”等3个任务,学生学会不同价态铁元素化合物的转化和检验方法,形成从元素价态和物质类别角度探究物质性质的思路。初步培养了实验探究能力,提升创新意识,发展基于“铁及其化合物价类二维模型建构”的模型认知素养。学生收获了真实新颖、亲身实践、分组合作、交流展示等成就性体验,制作的铁肥保存和合理使用说明书体现了项目式教学的本质特征,实现学习结果的可视性、共享性、交流性。     

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.     

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.     

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.