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-ethylenedii-mine-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-脱氧亚乙基二胺-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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