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Comparative Study on the Supramolecular AssembliesFormed by Calixpyridinium and Two Alginates with Different Viscosities

机译:超分子组装的比较研究由杯形吡啶鎓和两种不同粘度的藻酸盐形成

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摘要

In this work, a comparative study on the supramolecular assemblies formed by calixpyridinium and two alginates with different viscosities was performed. We found that sodium alginate (SA) with medium viscosity (SA-M) had a better capability to induce aggregation of calixpyridinium in comparison with SA with low viscosity (SA-L) because of the stronger electrostatic interactions between calixpyridinium and SA-M. Therefore, the morphology of calixpyridinium–SA-M supramolecular aggregates was a compact spherical structure, while that of calixpyridinium–SA-L supramolecular aggregates was an incompact lamellar structure. As a result, adding much more amount of 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt to calixpyridinium–SA-M solution was required to achieve the balance of the competitive binding, and in comparison with calixpyridinium–SA-L supramolecular aggregates, calixpyridinium–SA-M supramolecular aggregates were more sensitive to alkali. However, for the same reason, in comparison with calixpyridinium–SA-M supramolecular aggregates, calixpyridinium–SA-L supramolecularaggregates were much more stable in water not only at room temperaturebut also at a higher temperature, and even in salt solution. Therefore,in comparison with calixpyridinium–SA-L supramolecular aggregates,calixpyridinium–SA-M supramolecular aggregates exhibited acompletely opposite response to acid because of the generation ofsalt. Because SA is an important biomaterial with excellent biocompatibility,it is anticipated that this comparative study is extremely importantin constructing functional supramolecular biomaterials.
机译:在这项工作中,对杯盖吡啶鎓和两种不同粘度的藻酸盐形成的超分子组装进行了比较研究。我们发现中等粘度(SA-M)的海藻酸钠(SA)与低粘度(SA-L)的SA相比,具有更好的诱导杯状吡啶鎓聚集的能力,因为杯状吡啶鎓与SA-M之间的静电相互作用更强。因此,杯形吡啶鎓-SA-M超分子聚集体的形态为紧凑的球形结构,而杯形吡啶鎓-SA-L超分子聚集体的形态为紧凑的层状结构。因此,需要向杯盖吡啶鎓-SA-M溶液中添加更多量的1,3,6,8-py四磺酸四钠盐以达到竞争结合的平衡,并且与杯盖吡啶鎓-SA-L超分子聚集体相比,杯盖吡啶鎓-SA-M超分子聚集体对碱更敏感。但是,出于同样的原因,与杯盖吡啶鎓-SA-M超分子聚集体相比,杯盖吡啶鎓-SA-L超分子聚集体集料不仅在室温下在水中更稳定而且还要在更高的温度下,甚至在盐溶液中。因此,与杯盖吡啶鎓-SA-L超分子聚集体相比,杯盖吡啶鎓-SA-M超分子聚集体表现出由于产生了对酸完全相反的反应盐。由于SA是具有出色生物相容性的重要生物材料,可以预期,这项比较研究非常重要在构建功能性超分子生物材料中的应用。

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