两种吸附树脂对4B酸吸附行为的比较研究

研究了新型复合功能吸附树脂NDA-99和超高交联大孔吸附树脂JX-101对水溶液中4B酸(对甲苯胺-2-磺酸)的静态吸附行为和热力学特性，结果表明，NDA-99树脂对4B酸的吸附量明显大于JX-101树脂，两种树脂对4B酸的吸附均符合Freundlich吸附等温方程．其中，JX-101对4B酸的吸附属于物理吸附：NDA-99由于树脂表面存在弱碱性官能团，对4B酸的吸附表现为物理吸附和化学络合协同作用。     

几种吸附树脂对硝基化合物吸附性能的研究

研究NJ－8、AM－1、Amberlite XAD-4、JX－101 4种吸附树脂对对硝基苯乙酮和对硝基苯甲酸的静态吸附行为。结果表明：江苏南大戈德环保科技有限公司研制的NJ－8和AM－1两种吸附树脂对硝基化合物的吸附效果较好。并研究NJ－8型吸附树脂的动态吸附和脱附行为，结果显示：NJ－8型吸附树脂对对硝基苯甲酸的吸附容量为128mg/g干树脂，对对硝基苯乙酮的吸附容量为383mg/g干树脂。用8%NaOH:乙醇（体积比1：1）洗脱吸附酸的树脂，用甲醇或乙醇洗脱吸附酮的树脂，体积为5BV时，温度分别为333K和313K，脱附率均接近100％。     

大孔树脂对磺酸类化合物吸附行为的研究

用4种大孔树脂ND-022，ND-900，NDA-99和NDA-100作为吸附剂，分别对水溶液中甲基磺酸钠、苯磺酸钠、对甲基苯磺酸钠和2-萘磺酸钠等磺酸盐进行吸附．探讨了溶液的初始pH值对不同类型树脂吸附磺酸类物质的影响，并通过动态吸附实验研究了SO4^2-对树脂吸附磺酸盐的影响．实验结果表明，复合功能树脂NDA-99对磺酸类化合物具有良好的吸附性能，且其选择性优于弱碱树脂ND-900，这为进一步研究大孔树脂对磺酸类物质的吸附机理和实际工业应用提供了一定的理论依据。     

高分子材料的新领域——感光性树脂

感光性树脂在二十世纪五十年代之前,主要是用于印刷方面。利用天然高分子材料与红矾所制成的感光体系在印刷方面的尝试,已有一百多年的历史。在世界印刷史上,平印、凹印技术的发明,是基于这一发现的。这是印刷界一项重大的成就。二十世纪三十年代,随着合成树脂与塑料工业的发展,聚乙烯醇-重铬酸盐感光体系诞生,以后重氮、叠氮化物感光体系也相继问世。随着电子工业的迅速发展,感光性树脂 KPR 于五十年代初作为光致抗蚀剂出现于光刻技术中,成功地解决了微米级的图线的蚀刻,把电子工业向着微型与     

钇改性离子镀TiN膜的微观特性和附着机理

离子镀氮化钛(TiN)膜的应力状态和膜/基之间界面结构直接影响到涂层与基材的附着性。为了弄清涂层内部应力及界面结构对膜/基附着性的影响机理,人们对涂层自身应力和膜/基界面进行了一些相关的研究工作。我们通过添加钇离子镀TiN膜,借助钇的界面富集和改性作用,极大改善了TiN膜与基材的附着性。本文采用X射线线形分析法和透射电子显微镜(TEM)分析术,研究钇改性前后TiN膜内部微观应力和钇改性TiN膜[以Ti(Y)N表示]与A3钢基材界面的微观结构,从而探讨了涂层内部的微观应力和膜/基界面结构对其附着性的影响机理。     

纤维素基磁性聚偕氨肟树脂吸附Mn（Ⅶ）

用酸处理的纤维素基磁性聚偕氨肟树脂（AMAO）在溶液中吸附KMnO4，发生氧化还原反应的几率在2％以下；用碱处理的树脂（BMAO）作吸附剂，KMnO4还原为Mn（OH）4的比例剧增，达到或超过10％，并且与溶液的pH有关。但是，Mn（Ⅶ）被还原为Mn（Ⅳ）的量基本上不受KMnO4起始浓度、吸附剂添加量和吸附时间变化的影响。BMAO树脂吸附KMnO4的量是树脂偕氨肟基含量的5倍以上。超当量吸附现象反映了物理吸附的本质。     

2,5-取代-1,3,4-噁二唑化合物库的固相合成

本文使用组合化学方法以聚苯乙烯亚磺酸钠树脂（1）为载体合成了2，5-取代-1，3，4-二唑化合物库。树脂1首先与溴代乙酸乙酯反应生成聚合物支载的乙酸酯（2）。肼解后所得的肼树脂进一步与取代的苄氯反应得双欧讲树脂（4）。树脂4与三氯氧磷回流得聚合物支载的2，5-取代-1，3，4-二唑（5）。用W-溴代乙酰苯酮烷基化后聚合物支载的产物用三乙胺解脱得2-芳基-5-芳甲酰亚乙烯基-1，3，4-二唑化合物库，产率15％-36％。     

笼形聚偕胺肟树脂的研究—酚处理对树脂吸附贵金属性能的影响

研究了笼形聚偕胺肟树脂（CAO）和酸式（ACAO）及碱式（BCAO）树脂对于苯酚、对-氨基酚、对-硝基酚、对-甲氨基酚和对-苯二酚的吸附和吸留作用，测定了酚处理树脂的中和当量。它反映了笼形树脂吸留外来物的特性。酚处理树脂有效地吸附Ag 、AuCl4－、PtCl62-、PdCl42-和IrCl62-等贵金属离子，吸附方式似乎与溶液的pH值有关。SEM观察表明，Ag 、Au－Cl4-和IrCl62-离子在吸附过程中被还原为零价态，在树脂表面生成形态各异的结晶。     

弱碱性阴离子交换树脂分离1,6—二磷酸果糖的研究

采用弱碱性阴离子交换树脂HJ-30对发酵液中1，6-二磷酸果糖的分离进行了研究。详细地研究了树脂的吸附和脱附性能。实验结果表明，HJ-30树脂对FDP的吸附量达0．28gFDP／g湿树脂，以0．05mol／LNaCl洗脱光机磷和1mol／LNaCl洗脱1，6-二磷酸果糖，产品的收率和纯度分别为92％和99．4％。     

大孔吸附树脂提取穿心莲总内酯的研究

研究了大孔吸附树脂提取和纯化穿心莲总内酯的方法，采用HPLC法测定了穿心莲内酯的含量；考查了乙醇浓度对浸提效果的影响，并经动态吸附筛选了4种树脂；最后确定以ADS－7作为提取分离穿心莲总内酯的树脂，此树脂吸附量较高，脱附容量且能与杂质分离，有利于得到质量较好的穿心莲总内酯产品。     

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.