以研究生为主体力量构建化学科普平台的探索与实践

有效利用高校的科研和人才资源优势，依托陕西省"工科化学"实践教学示范中心，创建主要面向中小学生的化学科普平台。通过在科研团队基础上建设以研究生为主体、教师为指导的科普团队，并打造集知识学习、实践探索及兵器特色于一体的"ABC"科普课程体系，开设各类趣味化学及相关学科的实践项目，促进公众正确理解和认识化学，培养他们的科学精神进而提高科学素养。同时，参与科普工作也有效提升了研究生的实践能力，激发了他们从事科研的兴趣，也为研究生的培养开拓了一条新途径。     

化学类研究生培养国际化的研究——以青岛大学材料学科为例

以青岛大学化学类材料学科研究生培养国际化的研究为例,提出化学类研究生培养国际化的有效策略：（1）人才流动规模化;（2）平台建设国际化。以国内、国际产科教融合协同育人实训平台为依托,构建国内国际全方位产科教深度融合协同育人实训平台。形成了“平台搭建-学科建设-人才培养-反馈完善”的动态良性知识产业链循环,实现了研究生培养反馈、管理、评价机制,可作为全国省属高等院校化学类研究生培养国际化的推广模式。     

讲台与实验台互跨式研究生双语教学模式探索与实践

研究生双语教学是研究生教育国际化进程的必然要求。针对目前研究生双语教学中存在的问题,本文提出了一种新的研究生双语教学模式,即讲台与实验台互跨式研究生双语教学。以生物无机化学研究生双语课程为例,我们探索了讲台与实验台互跨式双语教学的实施方法。实践表明,讲台与实验台互跨式研究生双语教学模式解决了研究生培养中理论与实践相脱节的问题,不但可以全面提高研究生科研素质,而且可以提升教师科研水平。     

以“理-工-医”交叉融合实现源头创新——生物医学工程交叉学科研究生培养实践探索

针对科学技术和国家社会发展对生物医学创新型人才的需求，依托于学校的重大项目培育和新兴交叉学科研究课题，建立了生物医学工程与化学、物理、材料、电子和医学等"理-工-医"多学科交叉科研平台。基于"以人为本""全面发展"等现代教育理念和"以学生发展为中心"的高等教育思想，通过组建跨学科的研究生导师团，多导师联合指导，夯实学生多学科基础知识，加强学生对知识的理解和使用，拓宽研究生知识广度，着力培养研究生源头创新能力，打造研究生解决多学科交叉重要问题的能力。实践表明，多学科交叉科研平台在激发研究生源头创新思维、拓展专业知识、培养工程实践能力等方面起到重要的作用。对继续完善多学科交叉的研究生培养体系建设给出了建议。     

生物材料类大学生创新实验初探

为促进大学生积极参与国家大学生创新性实验计划项目,我院特推出“学业导师制”的管理模式,组织本科生按兴趣参加“科研训练”,并以科研小组为单位组织申报。以培养科研兴趣、加强科研训练、提高科研素养、实现科学理论与实验操作相结合为目的,就生物材料类项目的申请、组织实施、成果展示等方面提出相应的实施方案。     

本科生与研究生互动实验模式的探索与实践

提出了本科实验教学中本科生与研究生互动的实验教学“一二三模式”,旨在发挥科研与研究生的优势,为本科实验教学服务,提高本科实验教学质量,培养创新型人才。     

培养教育硕士专业学位研究生教学与科研技能的创新实践

为提高教育硕士专业学位研究生的培养质量,切实有效地解决人才培养中存在的实际问题,在内蒙古师范大学进行了“理论学习-实践训练-科学研究”三位一体的课程群教学改革与实践。通过任课教师和指导教师的教研合力,将多样化的有利于研究生教学能力和研究能力提高的实践活动有机地融合到专业学位课程的理论学习过程中,形成了教育硕士专业学位研究生教学和科研技能并重的创新培养模式。     

研究生参与实验室大型仪器管理的探索

阐述了研究生参与大型仪器管理的必要性、运行机制及实施环节,建立了"统一管理,专人负责,用管结合,开放使用"的管理模式.实践证明,这一措施的实施对规范大型仪器管理、提高仪器利用率以及实验室科研项目顺利进行起到了积极促进作用.     

中国科学院上海有机化学研究所

<正>中国科学院上海有机化学研究所成立于1950年5月,是一所历史悠久、集科研与教育为一体的国内外著名综合性研究机构。目前我所在学研究生441名。新建成的实验大楼、完备的实验条件、先进     

化学专业学术型硕士研究生培养与本科科研训练有效衔接的探究

阐述了高水平学术型硕士研究生培养与本科科研体验衔接的基本情况,以化学专业为例,就学术型硕士培养与本科创新性科研实践的衔接模式进行了详细的剖析,指出2者的衔接有助于高层次、高科研水平与高创新能力的硕士研究生培养。     

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.     

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%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

Synthesis of pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles by Curtius reaction in Morita-Baylis-Hillman derivatives

Synthesis of substituted pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles from the Morita-Baylis-Hillman derivatives of acrylates via saponification followed by Curtius reaction is described.     

正丁胺对激光染料荧光谱影响的研究

用正丁胺作为碳源,采用射频辉光放电制备碳膜,选用激光染料R6G和聚乙二醇混合液作为蒸气源,采用单源热蒸发,在蒸发室与染料同时沉积得到混合膜,用拉曼光谱和红外光谱分析了碳膜的结构和键合方式,分析表明:碳膜中存在胺基团和氢原子.混合膜的荧光谱测量结果表明,认为正丁胺对染料荧光谱的影响是因为胺基和氢原子的存在.     

Cu0-catalysed 1,3-dipolar cycloadditions of α-amino acid derived N,N-cyclic azomethine imines to ynones

A series of 20 CuAIAC reactions between eight 4-acylamino substituted pyrazolidine-3-one-1-azomethine imines and four terminal ynones were performed using Cu⁰ as catalyst. The corresponding fluorescent cycloadducts were obtained in very high yields upon simple workup. Thus, Cu-metal turned out to be a better catalyst than Cu^I in terms of yield and ease of isolation. Availability of azomethine imines, mild reaction conditions, and simple workup enable a “click” access to libraries of densely substituted 2,3-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-ones. Reactivity of differently substituted dipoles was evaluated experimentally and by quantum chemical methods (DFT).     

Synthesis and antioxidative/anti-inflammatory activity of novel fullerene–polyamine conjugates

(E)-4-(Fullerenopyrrolidin-1-yl)-3-methylbut-2-enoic acid and its corresponding succinimidyl ester, readily obtained through Prato-type modification of C₆₀, were used for the selective N-acylation of polyamines. The thus obtained conjugates were evaluated for their antioxidative and anti-inflammatory activity and their cytotoxicity was determined. Members of this family of compounds showed interesting anti-lipid peroxidation, anti-lipoxygenase and anti-inflammatory activity and comparable cytocompatibility to spermidine.