Ce0.67Zr0.33O2对CH4燃烧催化剂Fe2O3/Al2O3的改性作用

固定n(Ce)/n(Zr)比为0.67/0.33,用共沉淀法制得一系列CeO2-ZrO2-Al2O3固溶体.采用这些固溶体作载体,以Fe2O3为活性组分,用浸渍法制备了一系列催化剂.BET结果显示,将适量Ce0.67Zr0.33O2引入到Al2O3载体中有助于催化剂保持较高的比表面积.TPR结果显示,载体中引入适量的Ce0.67Zr0.33O2可以改善催化剂的氧化还原性能.XRD结果表明,Fe2O3在CeO2-ZrO2-Al2O3载体上呈现出良好的分散状况,老化前后催化剂的晶相结构基本无明显变化.特别是当载体中m(Ce0.67Zr0.33O2)∶m(Al2O3)的值为1∶2时,Fe2O3/CeO2-ZrO2-Al2O3催化剂在甲烷催化燃烧中显示出最佳的催化性能和抗高温老化性能.     

Synthesis of diethers derived from furoin by phase transfer catalysis under microwave irradiation

A series of new diethers were obtained by alkylation of furoin under microwave irradiation (MWI) in phase transfer catalysis (PTC) conditions. The products of alkyl halides were synthesized in good yields (>75%) within a few minutes, and the products of dihalides were synthesized in fair yields (about 45%). The yields are dramatically improved compared to conventional heating under the same conditions, in spite of similar profiles of rising in temperature.     

2,4,6—三氧—1,3,5,2—三氮磷杂环己烷衍生物的合成及其抗肿瘤活性

利用Ｎ，Ｎ－二（２－氯乙基）氨基磷酰二异氰酸酯和胺的加成反应，合成了２，４，６三氧－１，３，５，２三氮磷杂环己烷衍生物，它们的结构经＾１ＨＮＭＲ，ＩＲ和元素分析所证实。初步生物活性测试结果表明，部分化合物具有一定的抗肿瘤活性。     

离子液体介导CO2化学转化研究进展

The efficient utilization of carbon dioxide (CO₂) as a C1 feedstock is of great significance for green and sustainable development. Therefore, the efficient chemical conversion of CO₂ into value-added products has recently attracted a lot of research attention in recent years. The transformation of CO₂ generally requires high-energy substrates, specific catalysts, and harsh reaction conditions due to its high thermodynamic stability and kinetic inertness. Consequently, several efforts have been dedicated toward the development of high-performance catalysts and new reaction routes for CO₂ conversion over the last few decades. To date, many routes of convert CO₂ into value-added chemicals have been proposed, together with the development of heterogeneous and homogeneous catalysts. Among the advanced catalysts reported to date, ionic liquids (ILs) have been widely investigated and show great potential for the efficient, selective, and economical conversion of CO₂ into highly valuable products under mild conditions, even under ambient conditions. Some task-specific ILs have been designed with unique functional groups (e.g., —OH, —SO₃H, —NH₂, —COOH, and —C≡N), which can act as the solvent, absorbent, activating agent, catalyst, or cocatalyst to realize the transformation of CO₂ under metal-free and mild conditions. In addition, a variety of catalytic systems composed of ILs and metal catalysts have also been reported for the transformation of CO₂, in which the combination of the IL and metal catalyst is responsible for CO₂ conversion with high efficiency. In this review article, we summarize the recent advances in IL-mediated CO₂ transformation into chemicals prepared via C—O, C—N, C—S, C—H, and C—C bond forming processes. ILs that can chemically capture CO₂ with high capacity are first introduced, which can activate CO₂ via the formation of IL-based carbonates or carbamates, thus realizing the transformation of CO₂ under metal-free and mild conditions. Recent progress in IL-mediated CO₂ transformations to form carbonates and various kinds of N- and S-containing compounds (e.g., oxazolidinones, ureas, benzimidazolones, formamides, methylamines, benzothiazoles, and other chemicals) as well as CO₂ hydrogenation to give formic acid, methane, acetic acid, low-carbon alcohols, and hydrocarbons has been summarized in this review with a focus on the reaction routes, catalytic systems, and reaction mechanism. In these reactions, ILs can simultaneously activate the substrate via strong H-bonding in addition to activating CO₂, and the cooperative effects among the ionic and molecular species and metal catalysts accomplish the reactions of CO₂ with various kinds of substrates to afford a wide range of value-added chemicals. Finally, the shortcomings and perspectives of ILs are discussed. In short, IL-mediated CO₂ transformations provide green and effective routes for the synthesis of high-value chemicals, which may have great potential for a wide range of applications.     

SDS胶束对孔雀绿褪色反应的影响

研究了十二烷基硫酸钠（SDS）表而活性剂胶束和预胶束对孔雀绿褪色可逆反应的影响，建立了1－1型可逆反应的胶束催化模型和预胶束催化模型，获得了胶束相中正逆反应的速率常数和预胶束的平均聚集数．结果表明，SDS胶束和预胶束对正反应有禁阻作用，而对逆反应有催化作用．     

相转移催化法合成N—2—苯基—1,2,3—三唑—4—甲酰基—N′—芳基硫脲

报道了２－苯基－１，２，３－三唑－４－甲酰氯和硫氰酸铵在ＰＥＧ－４００固液相转移催化下与芳胺反应，制得一系列新的含２－苯基－１，２，３－三唑环的硫脲衍生物，并经ＩＲ，＾１ＨＮＭＲ和元素进行了结构确证。     

过渡金属复合氧化物电子组态与表面光伏响应的关系（Ⅰ）：M…

利用表面光电压谱及场诱导表面光电压谱研究了部分过渡金属复合氧化物的电子组态与其光伏响应的关系，结果表明，在过渡金属Ｍ（Ｍ＝Ｃｕ，Ｃｏ，Ｎｉ）铁酸盐系列样品中，开壳层的Ｃｕ和Ｃｏ的电荷转移跃迁具有双激发态的成分，其中含有较强的低能电子跃迁；与它们相比，闭壳层的Ｎｉ和铁酸盐的ＣＴ跃迁则需要较大的能量。     

纳米级金膜微电极的制作,表征及异相催化反应

报道了纳米级金膜微电极的制作方法，用ＸＰＳ及ＳＥＭ对电极表面进行了表征，考察了该电极的循环伏安及计时电流特性，在聚吡咯修饰微带金电极上成功地实现了葡萄糖氧化酶和电子传递媒体Ｆｅ（ＣＮ）６＾３－的同时固定，并研究了ＧＯＤ／Ｆｅ（ＣＮ）６＾３－／ＰＰｙ微酶电极对葡萄糖的响应，稳态响应电流与葡萄糖浓度之间存在Ｍｉｃｈｅａｌｉｓ－Ｍｅｎｔｅｎ动力学特征。     

八—4—(四氢糠氧基)双酞菁衍生物钕(Ⅲ)、铕(Ⅲ)的合成和LB膜的气敏性

八—４—（四氢糠氧基）双酞菁衍生物钕（Ⅲ）、铕（Ⅲ）的合成和ＬＢ膜的气敏性张引＊辛春梅王丹（吉林省教育学院化学系，长春１３００２２）梁冰洁＊＊陈文启席时权（中科院长春应用化学研究所，长春１３００２２）关键词：希土双酞菁衍生物ＬＢ膜气敏性荧光性紫外可见...     

非均相羰基氧化合成碳酸二苯酯反应液组分的分析

通过色质联用仪对非均相催化一步合成碳酸二苯酯(DPC)过程中的反应液的主要产物及副产物进行了定性分析，其结果发现该反应的主要副产物为苯氧基丙酸和4-苯氧基苯酚以及四丁基铵盐；用气相色谱外标法对反应液中的DPC进行了定量分析，并通过回归法得到了定量分析：DPC的计算方程式，实验证明该方程在DPC的浓度小于10％范围内比较可靠。