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首页> 外文期刊>Chemistry: A European journal >Supramolecular Assemblies of Sulfonatocalixarenes with Phenanthroline:Factors Governing Capsule Formation versus Bilayer Arrangements
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Supramolecular Assemblies of Sulfonatocalixarenes with Phenanthroline:Factors Governing Capsule Formation versus Bilayer Arrangements

机译:磺胺杯芳烃与菲咯啉的超分子组装:控制胶囊形成与双层排列的因素。

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Four crystalline complexes were prepared by the inclusion com-plexation of the 1,10-phenanthrolinium ion(Phen)with p-sulfonatothiacalix[4]-arene(TCAS)(2 from a solution at pH 1-2 and 4 from 1M HCl)and with p-sulfonatocalix[5]arene(C5AS)(3 from a solution at pH 1-2 and 5 from 1M HCl)upon varying the acidity of the solution.By combining the results obtained for complexes 2-5 with those for our previously reported complex(1),p-sulfonatocalix[4]arene(C4AS)complexed to Phen,it was revealed that p-sulfonatocalixarenes(CASs)form"bis-molecular"capsules(1,2,and 3)around Phen at pH 1-2,whereas complexes 4 and 5 display distinct host-guest inclusion behavior at higher acid concentrations.The degree of compactness of the capsules increases with the enlargement of the calixarene cavity,which is affected significantly by both the penetration depth of Phen and the structure of the Phen dimer.Furthermore,the complexation behavior of TCAS/C5AS with Phen in 1M DCl was investigated by using NMR spectroscopy,and was discussed in comparison with the previously reported results obtained from solutions at pH 2.0.
机译:通过将1,10-菲咯啉离子(Phen)与对-磺基噻唑杯[4]-芳烃(TCAS)包合络合制备四种晶体复合物(2来自pH 1-2的溶液和4来自1M HCl的溶液)并使用对-磺基磺酸杯[5]芳烃(C5AS)(3在pH 1-2的溶液中和3从1M HCl的溶液中)改变溶液的酸度。将配合物2-5的结果与我们的配合物相结合先前报道的复合物(1),对-磺基杯[4]芳烃(C4AS)与Phen复合,发现对-磺基杯芳烃(CASs)在pH值附近形成“双分子”胶囊(1,2和3)。在图1-2中,配合物4和5在较高的酸浓度下表现出明显的主客体夹杂行为。胶囊的致密程度随杯芳烃腔的扩大而增加,这受苯酚和苯酚的渗透深度的显着影响。此外,利用NMR光谱研究了TCAS / C5AS与Phen在1M DCl中的络合行为。 opy,并与先前报道的从pH 2.0溶液获得的结果进行了比较。

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