共查询到20条相似文献,搜索用时 93 毫秒
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采用荧光光谱法和核磁共振技术研究了对磺化杯[4]芳烃(SC4A)与盐酸可卡因(CH)间的超分子作用。研究了pH值、温度、离子强度和SC4A浓度对主客体超分子作用的影响。在pH7.5的Britton-Robinson缓冲溶液中,CH的荧光强度随着SC4A的加入而呈下降趋势,荧光的猝灭反映了CH-SC4A包合物的形成。通过光谱滴定法验证了主客体化合物的化学计量之比为1∶1。根据线性方程计算出CH-SC4A包合物的结合常数为6.93×104L/mol。1H NMR研究证明CH中含N—CH3的桥环部分局部进入SC4A的疏水空腔。密度泛函理论计算验证了这一作用机理。 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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叔丁基杯[6]芳烃的去叔丁基反应 总被引:4,自引:0,他引:4
报道了以对叔丁基杯[6]芳烃为原料,室温时,在三氯化铝催化下选择性脱去叔丁基的工艺.探讨了在合成去叔丁基杯[6]芳烃实验中催化剂用量对反应结果的影响,并对反应机理进行了讨论.结果表明,当n(AlCl3)∶n(p-tert-calix[6]arene)=8~9.5∶1时,分离得到了两种去叔丁基杯[6]芳烃:5-叔丁基-37,38,39,40,41,42-六羟基杯[6]芳烃和37,38,39,40,41,42-六羟基杯[6]芳烃,当n(AlCl3)∶n(p-tert-calix[6]arene)=10.5∶1时,得到37,38,39,40,41,42-六羟基杯[6]芳烃,产率90.8%. 相似文献
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首次合成一系列杯[10]冠醚。通过将对叔丁基杯[10]芳烃和乙二醇双对甲苯磺酸酯或多甘醇双对甲苯磺酸酯在K2CO3/甲苯或Cs2CO3/丙酮体系中反应,得到一系列杯[10]冠醚:1,2-杯[10]冠-4、1,3-杯[10]冠-2、1,2-,1,3-杯[10]冠-3、1,4-杯[10]冠-4、和1,6-杯[10]冠-4。 相似文献
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合成和表征了一个新的杯[4]芳烃衍生物,11,23-二羟亚胺甲基-25,27-二羟基-26,28-二丙氧基杯[4]芳烃 (B)及其与乙腈生成的组成为B·2CH3CN的化合物。1H NMR显示,在B·2CH3CN中B采取锥型构象,X-射线衍射分析确证在溶液中所发现的构象。在晶格网络中存在着B·2CH3CN以二聚体形式的自插入现象。在B3LYP/6-311G(d)水平上计算了该自插入二聚体中的非共价相互作用能,并对基集叠加误差进行了校正。在二聚体中的B·2CH3CN,一个CH3CN通过与羟亚胺基形成氢键使之稳定,结合能为–5.02 kJ·mol-1,另一个CH3CN则通过与另一个羟亚胺基形成氢键以及与另一B·2CH3CN中B苯环空腔间的C–H···π相互作用使之稳定,结合能分别为–14.23 kJ·mol-1和–3.77 kJ·mol-1。自插入的驱动能为–7.54 kJ·mol-1。 相似文献
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In the present work, we synthesised a functionalised calix[4]arene with 5,11-di(N-methyl-E-(4-pyridylethylene) moiety (CX[4]), and investigated interactions of it with HemiMeQ[6], HemiMeQ[7], and Q[8]) in both water and DMSO using fluorescence spectrophotometry and 1H NMR spectroscopy. Titration 1H NMR spectra revealed that Q[n]s prefers to include the N-methyl-E-(4-pyridylethylene) moiety. In particular, the interaction of CX[4] with Q[8] in water resulted in intense fluorescence emission, and this interaction system can respond to compounds such as amantadine. 相似文献
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S. J. Thibodeaux M. Sañchez Peña Y. Zhang S. A. Shamsi I. M. Warner 《Chromatographia》1999,49(3-4):142-146
Summary This work focuses on the separation and identification of p-tert butyl calix[4]arene derivatives. An isocratic mixture of
65% (v/v) acetonitrile and 35% (v/v) water with 0.1% (v/v) phosphoric acid was used as the mobile phase. A Bio-Rad Bio-Sil
ODS-5S (250 mm×4 mm) column was used as the stationary phase with UV detection of the analytes at 274 nm. The reversed-phase
high performance liquid chromatographic method which was developed provided baseline separation of five p-tertbutyl calix[4]arene
derivatives in twenty minutes. 相似文献
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Zouhair Asfari Sebastiano Pappalardo J. Vicens 《Journal of inclusion phenomena and macrocyclic chemistry》1992,14(2):189-192
A doubly-crowned calix and a double-calixcrown derived from 4,6,10,12,16,18,22,24,25,26,27, 28-dodecamethyl-5,11,17, 23-tetrahydroxycalix[4]arene (1) have been prepared by reaction of appropriate oligoethylene glycol ditosylates with (1) in acetonitrile in the presence of potassium carbonate. A potassium template effect is observed during one of the double cyclizations. 相似文献
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Ghosh K Semwal A Nayak SK Banerjee SB Banerjee M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2007,66(4-5):1122-1125
[60]- and [70]Fullerenes have been shown to form 1:1 supramolecular complexes with bis[2-(5,11,17,23,29,35-hexa-tert-butyl-37,38,39,40,41-pentahydroxycalix[6]arenyl-oxy ethyl ether) (1) and 5,11,17,23,29,35-hexa-tert-butyl-37,38,40,41-tetra hydroxyl-39,42-(crown-4)calix[6]arene (2) in CHCl3 medium by electronic absorption spectroscopy. Formation constants (K) of the complexes of [60]- and [70]fullerenes with 1 and 2 have been determined at room temperature from which free energy of formation values of the complexes have been estimated. The very high formation constant value of [60]fullerene/1 complex (5900 dm3 mol-1) in indicative of formation of inclusion complex. Moreover, PM3 calculations reveal that intermolecular interaction between [60]fullerene and 1 proceeds through quite deep energy molecular orbital. 相似文献
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新型杯[4]芳烃衍生物的合成 总被引:1,自引:0,他引:1
以对叔丁基杯[4]芳烃为起始原料,通过一步或两步取代反应合成了对叔丁基杯[4]芳烃的衍生物(1和2),其结构经FT-IR,^1H NMR,FAB-MS表征. 相似文献
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