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首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >The synthesis and molecular recognition study of β-cyclodextrin derivatives modified by spiro[2H-benzopyran-2,2′-indoline]
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The synthesis and molecular recognition study of β-cyclodextrin derivatives modified by spiro[2H-benzopyran-2,2′-indoline]

机译:螺[2H-苯并吡喃-2,2'-二氢吲哚]修饰的β-环糊精衍生物的合成及分子识别研究

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摘要

In this study, we adopted the condensation reaction between the aldehyde group in spiro[2H-benzopyran-2,2′-indoline] and the ethylene diamine in β-cyclodextrins to synthesize 1,3,3-trimethyl-6′-mono-(6-deoxy-ethylenediimine-β-cyclodextrin)-spiro[2H-benzopyran-2,2′-indoline] (β-CD-SPBI). The structure of the target compound was characterized by elemental analysis, NMR and IR spectroscopy. The UV–Vis and fluorescence spectroscopy were investigated in different solvents. The preliminary study of its molecular recognition was also conducted. The results indicated that β-CD-SPBI existed as two structural isomers, both of which showed significant fluorescent characteristics and β-CD-SPBI could showed the capacity of dual molecular recognition of a drug, ribavirin.
机译:在这项研究中,我们采用了螺[2H-苯并吡喃-2,2'-二氢吲哚]中的醛基与β-环糊精中的乙二胺之间的缩合反应,合成了1,3,3-三甲基-6'-单- (6-脱氧乙二亚胺-β-环糊精)-螺[2H-苯并吡喃-2,2'-二氢吲哚](β-CD-SPBI)。通过元素分析,NMR和IR光谱表征目标化合物的结构。在不同溶剂中研究了UV-Vis和荧光光谱。还对其分子识别进行了初步研究。结果表明,β-CD-SPBI具有两种结构异构体,均具有显着的荧光特性,β-CD-SPBI可以显示出对药物利巴韦林的双重分子识别能力。

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