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合成了上缘特丁基脱去的杯[4]芳烃25,27-二丁氧基-26,28-二(ω-十一碳烯氧基)杯[4]芳烃(p-H-C[4]B)及其相应的聚硅氧烷化高分子(PSO-p-H-C[4]B),以有上缘用N,N-二乙基氨甲基取代的杯[4]芳烃5,11,17,23-四(N,N-二乙基氨甲基)-25,26,27,28-四(ω-十一碳烯氧基)杯[4]芳烃(p-DEAM-C[4]U),并首次将它们用作毛细管柱气相色谱固定液,涂制成色谱柱,考察了这些杯[4]芳烃色谱柱的性能。结果表明,研制的杯[4]芳烃柱对芳香位置异构体均有良好的分离能力。 相似文献
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杯「4」芳烃以Cl(CH2CH2O)nTs(n=1,2)烷基化。得到65-87%的下缘带有2-氯乙氧基和2-(2-氯乙氧基)乙氧基怀「4」芳烃。 相似文献
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杯芳烃固定液分子识别的热力学性质 总被引:3,自引:0,他引:3
用毛细管气相色谱法测得了5组芳香族位置异构体在杯芳冠醚聚硅氧烷(C[4]C5_PSO),二乙氧基杯芳烃聚硅氧烷(C[4]E_PSO)和二丁氧基杯芳烃聚硅氧烷(M_C[4]B_PSO)3种杯芳烃固定液上的热力学参数ΔH、ΔS、ΔG,然后用热力学及超热力学的方法探讨了杯芳烃对异构体的分子识别特性和保留机理。 相似文献
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1,4—双(氯甲基)—2—甲氧基—5—壬氧基苯的均聚和共聚研究 总被引:1,自引:0,他引:1
以1,4-双(氯甲基)-2,5一二甲基苯(BCMDMB)和1,4-双氯甲基-2-甲氧基-5-壬氧基苯(BCMMONOB)为单体,采用脱氯化氢法,合成了聚(2,5-二甲基)对亚苯基亚乙烯(PDMPV)和聚(2-甲氧基-5-壬氧基)对亚苯基亚乙烯(PMONOPV);并对BCMDMB和BCMMONOB的共聚进行了研究。结果表明,适宜的反应条件为:碱与单体的摩尔比为20∶1,在室温下聚合时间为30h,碱的pH=14时产率最高。用IR、1H-NMR、UV—Vis对聚合物进行了表征。 相似文献
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以对取代酚亚甲基桥三聚体和2,6-二溴甲基对取代酚为原料,在TiCl4催化下环化得到6种新的含不同取代基[Cl,Br,CH3,C(CH3)3]的杯[4]芳烃衍生物,核磁共振谱研究表明:它们在溶液中的优势构象为锥形构象。 相似文献
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对-叔丁基杯[4]芳烃在环己烷中的激光光解研究*袁立华1姚思德2庄志豪1林念芸2(1.四川联合大学化学系成都610064)(2.中国科学院上海原子核研究所辐射化学实验室上海201800)关键词对-叔丁基杯[4]芳烃激光光解三线态中图分类号O621.2... 相似文献
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Summary Two new kinds of calix[4]arene derivatives, 5, 11, 17, 23-tetra-tert-butyl-25,27-bis(isopropylcarbamoyl-methoxy)-26,28-diundecenyloxy
calix[4]arene (C[4]A) and 25,27-dibutoxy-5, 11, 17, 23-tetra-tert-butyl-26,28-diundecenyloxy calix[4]arene (C[4]B0, are prepared
and then are polymized by two different processes. Three calix[4]arene polysiloxane stationary phases for capillary gas chromatography
are obtained. Their chromatographic characteristics, including column efficiency, polarity, selectivity, glass-transition
temperature and thermal stability are studied. Retention mechanisms are also discussed. 相似文献
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杯芳烃衍生聚合物用作毛细管气相色谱固定相的研究 总被引:13,自引:0,他引:13
合成了两种不同构象的杯芳烃衍生聚合物(杯芳冠醚聚硅氧烷c-c[4]c5-pso和二乙氧基杯[4]芳烃聚硅氧烷p-c[4]-pso),并将其用作毛细管气相色谱固定液,使用温度高达320℃,对不同的极性化合物,特别是对酚类异构体有很好的分离能力。同时也研究了分离机理。 相似文献
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含杯[4]芳烃毛细管固定相的制备与色谱性能 总被引:6,自引:2,他引:4
杯芳烃是由对位取代的苯酚在邻位通过亚甲基连接起来的环状化合物,由于具有可调节大小的空腔,不仅能络合无机离子,而且还可络合有机分子,在分析分离方面有极好的应用前景[1,2].杯芳烃已用于气相色谱[3,4]、离子选择性萃取[5,6]、液相色谱[7,8]和... 相似文献
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Calix[4]arene-capped [3-(2-O-beta-cyclodextrin)-2-hydroxypropoxy]propylsilyl-appended silica particles (C4CD-HPS), a new type of substituted beta-cyclodextrin-bonded chiral stationary phase (CSP) for high-performance liquid chromatography (HPLC), have been synthesized by treatment of bromoacetate-substituted [3-(2-O-beta-cyclodextrin)-2-hydroxypropoxy]propylsilyl-appended silica particles (BACD-HPS) with calix[4]arene oxyanions in anhydrous N-methyl-2-pyrrolidone. The synthetic stationary phase is characterized by means of elemental analysis. This new type of CSP has a chiral selector with two recognition sites: calix[4]arene and beta-cyclodextrin (beta-CD). The chromatographic behavior of C4CD-HPS was studied with several disubstituted benzenes and some chiral drug compounds under reversed-phase conditions. The results show that C4CD-HPS has excellent selectivity for the separation of aromatic positional isomers and enantiomers of chiral compounds due to the cooperative functioning of calix[4]arenes and beta-CDs. 相似文献
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[reaction: see text] Two new calix[6]arene derivatives 3 and 4 in a 1,4-anti conformation and one calix[8]arene derivative 5 were synthesized. SAMs of calix[n]arene (n = 4, 6, 8) derivatives 1-5 were formed on gold bead electrodes. Cyclic voltammetry with Ru(NH3)6(3+/2+) as a redox probe, together with impedance spectroscopy and reductive desorption, indicates that SAMs of 5 have a higher coverage than those of 3 and 4 due to the presence of hydrogen bonding and possibly its conformation. Noncovalent immobilization of C60 on gold surfaces was achieved with SAMs of calix[8]arene derivative 5 but not with those of 1-4. 相似文献
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Wanbo Liu Mikael A. Minier Andreas H. Franz Matthew Curtis 《Supramolecular chemistry》2013,25(12):806-818
In this study, calix[4]arene derivatives (11–14) bearing a single nucleobase (adenine, thymine, cytosine or guanine) were synthesised via click chemistry. The complexation ability of the synthesised derivatives with alkali metal ions was measured using MALDI-TOF mass spectrometry, and their molecular assembly in CDCl3 was determined using 1H NMR. Calix[4]arene derivatives (11–14) formed 1:1 complexes with all alkali metal ions and the rank order for the complexation selectivity was Rb+ > Cs+ > K+ ? Na+ > Li+. The attachment of nucleobase at the upper rim of calix[4]arene had little effect on its complexation selectivity for alkali metal ions. Thymine-, adenine- and guanine-calix[4]arenes formed self-assembled structures in CDCl3 via base–base interactions. In addition, adenine-calix[4]arene (11) bound to thymine-calix[4]arene (12) to form a discrete species via Hoogsteen hydrogen bonding. 相似文献