利用Word画图工具绘制化学思维导图

思维导图是利用“词汇”、“符号”、“图像”、“线条”、“颜色”的组合将大量复杂信息归纳分类形成具有关联性的知识网络结构的思维工具[1]。思维导图指实践主体运用图文并茂的技法把陈述性知     

大学有机化学“五维度”教学新策略——以“芳烃的亲电取代和亲核取代反应”为例

介绍了大学有机化学“强理念、重思维、活课堂、共育人、乐钻研”五维度教学新策略的内涵与实践。以线下教学为主,腾讯会议和慕课为辅助,践行“有机化学是科学也是艺术”的教学理念;采用多循环“疑探式”教学方式,辨析亲电试剂和亲核试剂的多样性;注重培养学生多种科学思维的综合运用;强化“文献预习”“练习讲解”“综合作业”“师生互动”等多个教学环节,加深学生对知识的理解与应用,提升学生在课堂中的参与度,着重培养学生的科学思维和人文素养、自主学习与团队合作精神。     

促进深度学习的专题复习教学*——以“碳及其化合物”为例

以促进学生的深度学习为基本理念,围绕“自然界的碳循环”“大气中CO₂的控减排”“化学家们合成的新型碳家族成员”等板块,设计并成功实施系列情境问题,在系列问题的讨论、分析、解决过程中帮助学生建构“碳”家族成员间相互转化的知识网络,提高学生思维的纵深度,引发高阶思维,促进深度学习。     

以层层深入的问题引导计算思维模型建构* ——以“化学反应中含杂质物质质量的计算”为例

针对学生在学习“依据化学方程式的计算”中普遍存在的“机械记忆解题步骤、怠于探求问题背后深层原因、将化学问题沦为单纯的数学计算”等倾向问题,采用层层深入的问题设置来激发学生深度思维,促使学生将已有知识链条化、结构化,同时将内在的思维链条外化,逐步搭建解决问题的一般思维模型,以此促进学生对化学核心概念和原理的深度理解。在初步建模的基础上,进一步引导学生对“化学反应中含杂质物质质量的计算”的具体问题再次建模,逐步形成“依据化学方程式的计算”类问题的解决图式。调查数据表明,经过思维建模及其应用有效发展了学生的深度思维能力和问题解决能力。     

以深度的科学探究促进初中生高阶思维能力发展*——以“酸和碱的中和反应”为例

针对学生在学习“酸和碱的中和反应”中普遍存在的“被动接受具体知识、缺失开展真实科学探究的思路、机械记忆中和反应规律、缺乏批判质疑精神及高阶思维能力不足”等倾向问题,设置了驱动性问题链协助学生搭建“情境问题”与“真实的科学探究”间的思路桥梁,在深度的科学探究中发展学生的发散性思维、有序思维、多角度分析问题、设计创造思维、逻辑严密的推理及评价反思等高阶思维能力。课堂教学中营造轻松、舒适的交流讨论环境,有益于学生之间碰撞出思维的火花、激发出创造的灵感。课堂观察表明,深度科学探究教学的实施,有效提升了学生的高阶思维能力及解决问题的能力。     

思维导图在仪器分析实验教学中的应用——以电化学分析实验为例

在电化学分析实验教学中引入思维导图,探讨了思维导图在仪器分析实验教学中的应用方法及效果评价。实验原理的教学依托“比较与对比图”和“逻辑思维图”,强调相关方法原理之间的联系,突出新方法的特点;实验步骤则以清晰易懂的“流程图”方式呈现。教学实践表明,思维导图有利于学生对实验基本原理的理解和掌握,提高了学生的实验兴趣,促进了学生的独立思考能力和解决问题的能力,显著提升了实验教学效果。     

落实核心概念功能价值演变的复习课教学——“溶液”单元复习

把“溶液”放到完整学科体系中,利用本原问题驱动,调取新授课储备的、与新问题情境匹配的学科理论、模型,将“核心概念、学科任务、认识角度、认识路径、能力活动、化学基本观念”融合,借助学科思维方式、方法,打通纵横联系,找寻基本规律,在思维碰撞中对自身原有认识加以修正、完善发展,形成“核心概念功能化,解决问题思路化”的系统思维模型。在学科核心素养统领下,落实核心概念功能价值演变的初中化学复习课教学。     

通过翻转课堂培养学生化学学科核心素养*——以“乙醇”为例

以翻转课堂“乙醇”为例,以思维导图为主要评价手段和表征阶段成果的方式。在翻转课堂教学过程中,促进了学生化学学科核心素养的培养。     

基于“雨课堂+对分易”的化工原理混合教学模式探索与实践*

根据新工科建设要求,应积极探索符合时代特征和工程教育规律的培养模式。针对化工原理课程特点,引入“雨课堂”和“对分易”2种现代网络教学平台作为混合式教学工具。雨课堂实现了课前-课中-课后的三环节教学模式;对分易通过提交章节思维导图及“亮考帮”作业,结合课堂讨论,逐一击破学生学习难点,多方位激发学生自主学习的积极性,增加了课堂互动性,提高了教学质量。     

以问题驱动培养初中生定量实验能力的实践*——以“测定混有碳酸钠的氯化钠样品中碳酸钠含量”为例

在搭建初中定量实验分析的思维模型的基础上,以“测定混有碳酸钠的氯化钠样品中碳酸钠含量”教学为例,在 “总问题”与“子问题”驱动下,引导初中生逐步建立解决定量实验问题的一般方法,提升对定量实验的设计、评价与改进能力,形成具有迁移价值的关键性能力。     

Di­methyl­phenyl­sulfonium tri­fluoro­methane­sulfonate and methyl­di­phenyl­sulfonium tri­fluoro­methane­sulfonate

The bonding geometry of sulfur in the cations of the title compounds, C₈H₁₁S⁺·CF₃SO₃^? and C₁₃H₁₃S⁺·CF₃SO₃^?, respectively, is similar and is independent of the ratio of the Me/Ph substituents. As expected, in both cations, the S—Ph bonds are somewhat shorter than the S—Me bonds. In both crystal structures, the interaction between cations and anions is similar.     

Methyl­tri­phenyl­stibonium tetra­fluoro­borate

In the title compound, [Sb(CH₃)(C₆H₅)₃]BF₄, there are four independent cations and anions in the asymmetric unit. The geometry around the Sb atom is distorted tetrahedral, with Sb—C distances in the range 2.077 (4)–2.099 (10) Å and angles at the Sb atom in the range 103.3 (3)–119.0 (4)°.     

2,4,6‐Tri­chloro­phenyl­iso­nitrile and 2,4,6‐tri­chloro­benzo­nitrile

The molecular structures of the title compounds, 2,4,6‐tri­chloro­phenyl­iso­nitrile (IUPAC name: 2,4,6‐tri­chloro­phenyl isocyanide), C₇H₂Cl₃N, and 2,4,6‐tri­chloro­benzo­nitrile, C₇H₂Cl₃N, are normal. The two structures are not isomorphous, but do contain similar two‐dimensional layers in which pairs of mol­ecules are held together by pairs of Cl?CN [3.245 (3) Å] or Cl?NC [3.153 (2) Å] interactions. The two‐dimensional isomorphism is lost through different layer‐stacking modes.     

{[(N‐Methyl‐p‐toluidino)­di­phenyl­phospho­ranyl­idene]­methyl}(N‐methyl‐p‐toluidino)­di­phenyl­phospho­nium iodide

The cationic part of the homodifunctional amino­phospho­ranyl ligand, C₄₁H₄₁N₂P₂⁺·I^?, shows interesting features associated with the N—P—C—P—N skeleton. The P—C(H) bond distances [1.696 (3) and 1.697 (3) Å] possess partial double‐bond characteristics. The nature of the P—C(H) and P—N bonds suggests that the positive charge is only distributed around the P—C—P atoms. The structure has near twofold symmetry through the central methyl­ide‐C atom.     

Ethyl­tri­phenyl­phospho­nium perrhenate and (iodo­methyl)­tri­phenyl­phospho­nium perrhenate

Ethyl­tri­phenyl­phospho­nium perrhenate, (C₂₀H₂₀P)[ReO₄], and (iodo­methyl)­tri­phenyl­phospho­nium perrhenate, (C₁₉H₁₇IP)[ReO₄], have been crystallized from 2‐propanol. Both crystal structures consist of phospho­nium cations and perrhenate anions. The cations show the typical propeller‐like geometry. In both crystals, the positions of the nearly tetrahedral anions are stabilized by weak C—H⋯O hydrogen bonds, and for the latter compound, I⋯π interactions also occur.     

2,4‐Di­nitro­phenyl­hydrazones of 2,4‐di­hydroxy­benz­aldehyde, 2,4‐di­hydroxy­aceto­phenone and 2,4‐di­hydroxy­benzo­phenone

In 2,4‐di­hydroxy­benz­aldehyde 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­form­amide solvate {or 4‐[(2,4‐di­nitro­phenyl)­hydrazono­methyl]­benzene‐1,3‐diol N,N‐di­methyl­form­amide solvate}, C₁₃H₁₀N₄O₆·C₃H₇NO, (X), 2,4‐di­hydroxy­aceto­phenone 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­form­am­ide solvate (or 4‐{1‐[(2,4‐di­nitro­phenyl)hydrazono]ethyl}benzene‐1,3‐diol N,N‐di­methyl­form­amide solvate), C₁₄H₁₂N₄O₆·C₃H₇NO, (XI), and 2,4‐di­hydroxy­benzo­phenone 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­acet­amide solvate (or 4‐­{[(2,4‐di­nitro­phenyl)hydrazono]phenyl­methyl}benzene‐1,3‐diol N,N‐di­methyl­acet­amide solvate), C₁₉H₁₄N₄O₆·C₄H₉NO, (XII), the molecules all lack a center of symmetry, crystallize in centrosymmetric space groups and have been observed to exhibit non‐linear optical activity. In each case, the hydrazone skeleton is fairly planar, facilitated by the presence of two intramolecular hydrogen bonds and some partial N—N double‐bond character. Each molecule is hydrogen bonded to one solvent mol­ecule.     

LiF-LiCl-LiVO<Subscript>3</Subscript>-Li<Subscript>2</Subscript>SO<Subscript>4</Subscript>-Li<Subscript>2</Subscript>MoO<Subscript>4</Subscript> system

Phase equilibria in the LiF-LiCl-LiVO₃-Li₂SO₄-Li₂MoO₄ system have been studied by differential thermal analysis. The eutectic composition has been determined as follows (mol %): LiF, 17.4; LiCl, 42.0; LiVO₃, 17.4; Li₂SO₄, 11.6; and Li₂MoO₄, 11.6, with the melting temperature equal to 363°C and the enthalpy of melting equal to (284 ± 7) kJ/kg.     

Chemical durability of MoO<Subscript>3</Subscript>-P<Subscript>2</Subscript>O<Subscript>5</Subscript> and K<Subscript>2</Subscript>O-MoO<Subscript>3</Subscript>-P<Subscript>2</Subscript>O<Subscript>5</Subscript> glasses

Thermal and chemical durability studies of the phosphate glasses belonging to the binary MoO₃-P₂O₅ and the ternary K₂O-MoO₃-P₂O₅ systems are reported. The chemical resistant attack tests carried out on the free alkaline MoO₃-P₂O₅ glasses show that the glass associated with the P/Mo ratio 2 has the high chemical durability. It shows also a high glass transition temperature value. The above findings are interpreted in terms of the cross-link density of the glasses and the strength of the M-O bonds (M=P, Mo). The influence of K₂O addition on the properties (density, T _g, durability) of this binary high water resistant glass is studied. It is found that the chemical durability along with the other physical properties are reduced by the incroporation of K₂O in the glass matrix. The results were explained by assuming the formation of non-bridging oxygens and weak bonds. The mechanism of the dissolution of these glasses is proposed.     

3‐O‐Acetyl‐4‐deoxy‐4‐iodo‐β‐d‐fructo­furan­osyl 2,3,6‐tri‐O‐acetyl‐4‐chloro‐4‐deoxy‐α‐d‐gluco­pyran­oside

At 160 K, the gluco­pyran­osyl ring of the title compound, C₂₀H₂₈ClIO₁₃, has a near‐ideal ⁴C₁ conformation and the fructo­furan­osyl ring has a twist ⁴T₃ conformation. The two hydroxy groups are involved in intra‐ and intermolecular hydrogen bonds, with the latter interactions linking the mol­ecules into infinite one‐dimensional chains. The absolute configuration of the mol­ecule has been determined.