建立教学、科研、生产三结合的教学新体系

南开大学高分子化学研究所坚持科研既要促进学科发展、培养人材,又要繁荣经济、为四个现代化服务的指导思想,实行研究所办工厂,建立教学与科研、生产三结合的教学新体系,加强专业、课程、教材、实验室等基本建设,在提高教学质量、培养研究生、开展基础研究和应用研究、发展生产等方面,取得了显著的成果。在教学方面,现有23名硕士研究生和9名博士研究生在高分子所学习。在科研方面,现设有离子交换树脂与吸附树脂一室、二室、高分子试剂、生物技术、高分子催化剂、高分子表征和高分子物理与物化等7个实验     

试剂级离子交换树脂和吸附树脂的开发与生产

随着科学技术的不断发展,在许多学科领域的科学研究中都用到不同性能的离子交换树脂、吸附树脂、高分子试剂和高分子催化剂等,仅仅依靠工业化的树脂品种已远远不能满足这种需求。为了国内外学者在科研中能够方便地获得所需的各种类型的树脂,很有必要开展试剂     

中国科大功能高分子课程教学四十年

<正>功能高分子出现于上世纪中叶，以离子交换树脂和螯合树脂为代表，派生出化学功能型高分子，催生了固相合成的诞生。上世纪中后期，功能高分子在电学、光学和生物学等领域得到了广泛研究和应用。时至今日，功能高分子不仅有着广泛的实际应用，而且也成为高分子、材料以及其他学科的重要研究对象，成为促进国家高水平持续发展的关键材料。为推动我国功能高分子领域的基础研究和应用开发的创新性发展，加强并做好该领域的人才培养，功能高分子课程教学是不可或缺的环节。     

石蜡基微胶囊相变材料研究进展北大核心CSCD

本文从微胶囊壁材出发,重点介绍了石蜡基/高分子、无机和高分子-无机杂化壳微胶囊的制备及应用,并总结了上述微胶囊的优势和不足。其中石蜡基/高分子壳微胶囊的壁材包括三聚氰胺-甲醛树脂、脲醛树脂、三聚氰胺-甲醛-尿素树脂、聚氨酯树脂、丙烯酸树脂等,石蜡基/无机壳微胶囊的壁材包括二氧化硅、二氧化钛、碳酸钙、氧化锌等,石蜡基/高分子-无机杂化壳的壁材包括三聚氰胺-甲醛树脂、三聚氰胺-甲醛-尿素树脂、丙烯酸树脂等与二氧化钛、二氧化硅等无机粒子复合。并对石蜡基微胶囊相变材料的未来发展方向和应用前景进行展望,以期为今后研究提供借鉴。     

吸附树脂和离子交换树脂研究的新进展——介绍南开大学高分子化学研究所的部分工作

本文介绍了南开大学高分子化学研究所近年来在吸附树脂、离子交换树脂和某些具有络合基因的树脂的合成、性能和应用方面的最新研究成果。     

智能高分子材料

本文介绍了形状记忆树脂、高分子凝胶、本征导电聚合物、高分子复合材料、高分子薄膜、超分子聚合物、液晶聚合物等智能高分子材料的一般概念及其应用的一些方面。     

无皂相反转乳化法制备高分子水基分散体系

高分子树脂水基分散体系是指高分子树脂以微粒形式分散于水中, 包括高分子乳液、高分子悬浮液等体系. 由于高分子树脂水基分散体系具有低成本, 高性能, 无污染等优点, 一直受到普遍关注.     

南开大学在离子交换与吸附科学技术领域的部分成果简介

在何炳林教授指导下,经过三十多年的发展,南开大学在离子交换树脂与吸附树脂的研究与生产方面,已形成了一个完整的体系。该校高分子化学研究所,化学系,高分子化学研究所所办化工厂,生物系,分子生物研究所和校测试分析中心密切配合,并与全国各地的有关单位进行协作,在新树脂的研制与生产,树脂性能的测试、树脂的应用和基础理论研究诸方面,取得了一系列重要的科研成果,尤其是吸附树脂的研究,已达到国际先进水平。我们选取了该校在这一领域中的部分科技成果作简略介绍,以飧读者。     

我国高分子学科发展动态与国家自然科学基金概述

汇总了高分子学科近期的发展情况,介绍了国内高分子部分研究与开发进展,概述了几次学科研讨会所探讨的基本问题。在国家自然科学基金介绍中,着重强调了获资助单位分布广泛性增加、申请数增长偏慢和选题应该更多地关注高分子应用中的基本科学问题,还探讨了国家自然科学基金申请写作注意事项。     

晶须及其在高分子材料中的应用

简要介绍了目前高分子材料改性中常用的晶须，如钛酸钾晶须、硼酸铝晶须、氧化锌晶须等，主要对其在橡胶、热塑性弹性体、热塑性树脂以及热固性树脂中的应用作了详尽论述。     

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.     

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.     

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.     

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.