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首页> 外文期刊>Journal of the Chemical Society, Perkin Transactions 1 >Synthesis and complexation properties of C-pivot lariat ethers containing 16-crown-5, 19-crown-6 and 22-crown-7 rings toward alkali metal cations
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Synthesis and complexation properties of C-pivot lariat ethers containing 16-crown-5, 19-crown-6 and 22-crown-7 rings toward alkali metal cations

机译:含16冠5、19冠6和22冠7环的C-枢轴套索状醚对碱金属阳离子的合成和络合特性

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A new series of C-pivot lariat ethers 1-5 having an oxyquinoline moiety as part of the electron-donating sidearm were obtained from crown ether derivatives of low symmetry such as 3n-methylene-(3n + 1)-crown-n (n = 5, 6, 7) and their complexation properties toward alkali metal cations were evaluated by measuring the extractability, stability constant in THF, characteristic absorption in the UV spectrum in THE and passive transport ability. The difference in the skeletal structure of the pivot position of the lariat ethers 1a and 4 was found to remarkably affect their complexation properties; that is, the former having a 2-methylglycerol structure around the pivot carbon showed much higher complexing ability than did the latter. The effect of the crown ring size and the number of heteroatoms of the electron-donating sidearm on the complexation properties was also examined and discussed. As a result, K+ selectivity was attained by 16-crown-5 and 19-crown-6 derivatives (1 and 2), whereas 22-crown-7 derivatives 3 showed Rb+ selectivity. [References: 43]
机译:从低对称度的冠醚衍生物(例如3n-亚甲基-(3n + 1)-冠-n(n)中获得了一系列新的具有氧喹啉部分作为给电子侧臂一部分的C-枢轴套索醚1-5 = 5、6、7)和它们对碱金属阳离子的络合性能通过测量可萃取性,在THF中的稳定常数,在THE中UV光谱中的特征吸收和被动传输能力来评估。发现套索状醚1a和4的枢轴位置的骨架结构上的差异显着影响了它们的络合性质。也就是说,前者在枢轴碳周围具有2-甲基甘油结构显示出比后者高得多的络合能力。还研究并讨论了冠环尺寸和供电子侧臂杂原子数目对络合性能的影响。结果,通过16-冠-5和19-冠-6衍生物(1和2)获得了K +选择性,而22-冠-7衍生物3显示了Rb +选择性。 [参考:43]

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