形式电荷之辨析与应用

从基础的元素化学和化学结构理论入手,系统性地举例辨析形式电荷的若干相关问题,讨论其与真实电荷、化合价、氧化态和电子对之别,并举例在前沿金属配合物等领域的应用。以期对化学基础教学与推广有助。     

利用中心原子价层轨道阐释软硬酸碱理论的原理与应用

软硬酸碱理论作为基础化学的重要理论,其在教学与教材中却存在定义不清、难以应用、适用范围不明、模棱两可等众多问题。借用前线轨道理论的观念,针对核心原子的外层轨道进行系统性讨论,并分类举例说明其适用范围与应用方式,以期对基础教学和相关科研有助。     

以催化应用为纽带链接基础化学2课程与多学科的交叉融合

“基础化学2”是面向“基础学科拔尖学生培养计划”大一本科生开设的一门理科专业基础课。针对学生因专业选择余地大容易觉得课程与专业联系不够紧密而学习积极性不高的问题，提出以元素及其化合物的催化应用为纽带，寻找合适的切入点，将化学基础知识与各相关学科研究前沿及工业应用相联系，建设具有学科交叉特色的基础化学教学体系的建议，突出培养学生的学科创新思维能力，体现理论与实践相结合的教学特色。     

医学化学学科教学知识构建的初探

护理专业学生文理兼收,文科学生学习医学化学面临很大困难,为此研究化学学习中的认知规律,加大医学化学课程的改革力度,建构化学教师的学科教学知识结构和医学化学学科教学知识的基本理论,达到提高教学质量的目的。     

试论化学教学论的基础

化学教学理论界对化学教学论的基础是什么的回答不深不透,已深度影响到化学教学论自身的建设。本文认为化学教学实践活动应是化学教学论的实践基础;普通教学论、教育心理学、教育社会学、教育传播学应是化学教学论的主要理论基础,而教育学原理是通过普通教学论对化学教学论发挥指导作用的。鉴此,理清了化学教学论与相关理论学科及化学教学实践活动的关系层次。提出化学教学论要以普通教学论、教育心理学、教育社会学、教育传播学的研究终点作为自己的研究起点,基于实存的化学教学实践活动构建化学教学论体系。     

化学哲学:化学学科理解维度解构与水平提升路径

经文献分析发现在化学学科理解相关研究中出现一个共性问题,即对化学学科理解的对象认知不一,具有不同程度的差异性。基于此,通过对化学学科理解对象的文献观点分析发现,文献所述化学学科理解对象皆差异性地指向化学知识、化学史及化学哲学三大范畴,但其指向化学哲学的过程是不自觉的、不系统的。因此通过分析化学哲学本体、化学教学的理论基础及其本质、化学教学与化学哲学的“供需”关系,探讨基于化学哲学视角系统梳理化学学科理解对象的可行性、合理性及必要性。最终认为化学哲学是一个系统且具学理性的化学学科理解维度解构路径,同时也是认知主体获得深度且系统的化学学科理解的水平提升路径。     

将矿物学理论与实验知识引入基础无机化学教学的探讨

矿物学是与无机化学密不可分的兄弟学科之一。无机化学知识的一个重要来源就是人类对矿物的观察与研究,同时元素化学的基础研究也被广泛应用于矿物学。对于矿物的认识可以加深学生对于无机化学理论联系实际的感性和理性认识,并进一步熟悉相关元素的性质。本文从基础无机化学教学的角度整理了矿物学的理论与实验教学要点,并以多种典型矿物为实验对象描述其实验性质,并阐述如何结合矿物实例进行矿物学理论与实验的教学。将矿物学相关内容引入基础无机化学教学,不失为一种交叉学科与基础化学教育相结合的新模式。     

医用基础化学教材改革的几点思考

化学是医学、药学和生物学的重要基础。特别是近年来分子生物学(molecularbiology)、分子医学(molecularmedicine),遗传组学(genomics)、蛋白组学(proteomics)、代谢组学(metabonomics)等学科的相继出现,标志着生命科学的发展进入了分子水平,化学在生命科学中的重要性更加突出。如何不失时机地将化学学科作为一个基础学科整体介绍给医学、药学和生物学的学生,又在教学中将化学与医学、药学和生物学的紧密联系介绍给学生,从而构建出一套对医学、药学和生物学学生适用的生物医药类专业化学基础课体系,并在此基础上,搭建为生物医药类专业学生服…     

综合性大学通识课程“化学与健康”的教学探索

通识课程是高校专业教学内容的重要组成部分,对于提高本科人才培养质量具有深远的作用。通识课“化学与健康”的教学内容涉及化学、生命、药学、医学、环境等学科。该课程可以拓宽学生知识面、促进多学科交叉,达到提高科学素养的目的。以通识课“化学与健康”教学实践为基础,针对综合性大学该课程的建设基础、课程目标及教学内容设计、教学方法与手段、教学效果、思政元素的引入等方面进行了讨论,调研了国外相关课程设置的特点,为加强高校、尤其是综合性大学通识课程的建设提供参考。     

化学理论与机制发展规划概述

化学理论与机制是化学科学的理论基础,其根本任务是研究化学科学中的基本原理,揭示化学反应及其相关过程的机制和基本规律,并为其他相关学科的发展提供基础理论支撑.本文简要介绍了国家自然科学基金委员会化学科学部化学理论与机制领域(基金申请代码:B03)"十四五"及中长期发展规划、学科布局、申请代码和研究方向,供相关人员参考.新...     

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.