Synthesis and crystal structure of Ni,Cu complexes of 5-methyl-10,10,15,15,20,20-hexaethylcalix[4]pyrrole mono-Schiff bases

The functionalized calix[4]pyrrole meso-substituted Schiff bases were conveniently prepared by fourstep synthetic route. Furthermore, the nickel and copper complexes of calix[4]pyrrolemeso-substituted Schiff base with 1:2 stoichiometry were obtained. The crystal structures of the calix[4]pyrroles and their metal complexes were determined by X-ray diffraction.     

Synthesis and characterization of bis-[1]rotaxanes via salen-bridged bis-pillar[5]arenes

The series of salen-bridged bis-pillar[1]arenes were conveniently prepared by condensation reaction of5,5'-methylenebis(2-hydroxybenzalde hyde)or 5,5'-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde)with mono-amido-functionalized pillar[5]arenes containing different terminal aminoalkyl groups in refluxing ethanol.The^1H NMR and 2D-NOESY spectra indicated that the salen-bridged bis-pillar[5]arenes with longer allcylene linker(n=3,4,6)formed the fascinating bis-[1]rotaxanes,while the salenbridged bis-pillar[5]arenes with short hydrazine and ethylenediamino linker(n=0,2)predominately existed in free form.The single crystal structure of the bis-pillar[5]are ne ambiguously indicated that two propylenediamino linker inserted in to two cavities of pillar[5]arene to form a novel bis-[1]rotaxanes.     

糖基修饰大环化合物的研究进展

糖类分子作为生命过程中多种特殊受体的底物,在生物信息传递中发挥着重要的作用.近年来,已通过各种方法高效率地制备了一些新型的糖基修饰的杯芳烃、环糊精和冠醚等大环分子,它们在生物凝集素特异性识别、选择性离子识别及手性催化等方面的应用引起了研究者的广泛兴趣.本文从糖基修饰大环分子的合成、功能化及其相关应用方面综述了目前糖基功...     

Microporous polycarbazole with high specific surface area for gas storage and separation

Microporous polycarbazole via straightforward carbazole-based oxidative coupling polymerization is reported. The synthesis route exhibits cost-effective advantages, which are essential for scale-up preparation. The Brunauer-Emmett-Teller specific surface area for obtained polymer is up to 2220 m(2) g(-1). Gas (H(2) and CO(2)) adsorption isotherms show that its hydrogen storage can reach to 2.80 wt % (1.0 bar and 77 K) and the uptake capacity for carbon dioxide is up to 21.2 wt % (1.0 bar and 273 K), which show a promising potential for clean energy application and environmental field. Furthermore, the high selectivity toward CO(2) over N(2) and CH(4) makes the obtained polymer possess potential application in gas separation.     

蝶状铁硒簇合物双(μ-P-甲苯硒基)六羰基二铁双膦取代衍生物的~1H和~(13)CNMR谱的归属研究

测得并解析了2个蝶状铁硒取代衍生物（μ-p-MeC6H4Se）2Fe2（CO）。（PH2PCH2CH2PPH2）（A）和（μ-P-MeC6H4Se）2Fe2（CO）4（cis-Ph2PCH=CHPPh2）（B）的1H-1HCOSY谱和1H-13CCOSY谱以及A的1H－1HNOESY谱，从而进一步确证了它们的结构．     

间苯二酚杯芳烃树枝醇类化合物的合成

用间苯二酚杯芳烃的氧代乙酸乙酯类衍生物1a～1b分别与三羟甲基甲胺和二乙醇胺在乙醇/甲苯中进行酰胺化反应, 合成了四种新型的间苯二酚杯芳烃树枝醇化合物2a～2d, 树枝醇2a～2d外缘的羟基用乙酸酐酯化, 得到全乙酰基衍生物3a～3d. 化合物结构都用¹H NMR, IR和元素分析等方法进行了表征, 对树枝醇化合物的聚集状态进行了光学显微镜观察.     

One-pot multicomponent synthesis of substituted 5,7-dihydro-1,6-naphthyridines and 5,6,7,8-tetrahydroquinolines

An one-pot approach was developed for the synthesis of substituted 5,7-dihydro-1,6-naphthyridines and 5,6,7,8-tetrahydroquinolines with moderate to good yields. This pathway is a modified two-step synthesis of Kröhnke pyridine and involves a four-component tandem reaction of N-phenacylpyridinium bromide, aromatic aldehydes, substituted or nitrogen-containing cyclic ketones and a nitrogen source. This multi-component reaction is performed using microwave irradiation heating of the reaction substrates under an environment of NH₄OAc/HOAc.

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