排序方式: 共有73条查询结果,搜索用时 15 毫秒
1.
Yu Liu Yong Chen Shi-Zhao Kang Li Li Chun-Hua Diao Heng-Yi Zhang 《Journal of inclusion phenomena and macrocyclic chemistry》2003,47(1-2):91-95
Two novel benzo-15-crown-5 tethered β-cyclodextrins 1 and 2have been synthesized by coupling substituted benzo-15-crown-5 with correspondingβ-cyclodextrin derivatives. Their inclusion complexation behavior withrepresentative guests, such as cyclohexanol, cyclohexane carboxylic acid, cyclohexaneacetic acid, sodium cyclohexane carboxylate, and potassium cyclohexane carboxylate,was investigated in aqueous solution by means of fluorescence spectrometry. As compared with parent β-cyclodextrin, benzo-15-crown-5 tethered β-cyclodextrins 1–2 display significantly enhanced molecular binding abilities and selectivities towards model substrates, especially towards substrates containing alkali-metal cations. These results indicate that, bearing two recognition sites in a single molecule, these supramolecular architectures can strongly enhance the molecular binding ability of parent β-cyclodextrin by the cooperative binding of the β-cyclodextrin cavity and the crown ether moiety. Possessing a shorter linker, crown ether-β-cyclodextrin 2 shows much higher binding affinity with guest molecules than crown ether-β-cyclodextrin 1, which may be attributed to the binding size and molecular multiple recognition behavior between host and guest. 相似文献
2.
3.
A water-soluble nanometer-scale metallocapped polyrotaxane has been prepared by the inclusion complexation of azo-calixarenes with metallo-bridged bis(beta-CD)s, displaying highly selective binding for Ca(2+). 相似文献
4.
A novel bis(beta-cyclodextrin) was synthesized, and its binding behavior with steroids was investigated to demonstrate that the cooperative co-inclusion of guest and tether by two cyclodextrin moieties is operative to afford the highest molecular selectivity of up to 3.6 for deoxycholate over taurocholate. 相似文献
5.
Two constitutional isomers of dibenzo-18-crown-6 derivatives (6 and 7) were synthesised and their binding behaviours towards trivalent lanthanoid cations (La3 + , Ce3 + , Pr3 + , Nd3 + , Sm3 + , Eu3 + , Gd3 + and Tb3 + ) were investigated. Both isomers expressed better binding affinities towards Sm3 + and Tb3 + than a group of other lanthanoids, as measured by the ligand-to-metal charge-transfer (LMCT) band intensity at ca. 425 nm using UV–vis spectroscopic method. Additionally, the trans isomer 7 was shown to have a higher binding ability than the cis isomer 6 towards Tb3 + . 相似文献
6.
A new diarylheptanoid glucoside,(8R,9R)-17-methoxy-2-oxatricyclo[13.2.2.13.7]icosa-l(17),3(20),4,6, 15,18-hexaene-4,9,10-triol-9-O-β-D-glucopyranoside(1),namely jugcathayenoside,together with two known diarylheptanoids,(+)-galeon(2) and 4-hydroxy-17-methoxy-2-oxatricyclo[13.2.2.13,7 ]icosa-1(17),3(20),4,6,15,18-hexaene-9-one(3),were isolated from the root bark of Juglans cathayensis. Their structures were elucidated on the basis of extensive spectroscopic data analysis. 相似文献
7.
8.
本文通过Click化学反应合成了一种含喹啉基和三唑基的开链冠醚, 考察和比较了主体化合物对镉等金属离子的荧光传感和选择性键合行为, 并通过荧光和核磁等手段研究了溶剂对其荧光传感的影响. 相似文献
9.
合成了一种18-冠-6修饰的苝酰亚胺衍生物(1), 研究了其作为主体对金属离子与阴离子的选择性识别行为. 结果表明, 主体1对Ba2+离子具有一定的选择性响应, 并可以通过Ba2+调控主体1的堆积行为; 主体1还对F-离子有选择性响应, F-与苝酰亚胺单元之间发生了阴离子-π相互作用. 相似文献
10.
In the presence of 1,2-bis(4,4'-dipyridinium)ethane, p-sulfonatocalix[5]arene (C5AS) adopts an unseen partial-cone conformation to form back-to-back dimers, whereas C5AS crystallizes in face-to-face dimers to form a wavy layer, rather than the expected bilayer, arrangement upon complexation with 1,2-bis(pyridinium)ethane. 相似文献