Sulfate-Templated 2D Anion-Layered Supramolecular Self-Assemblies

被引:36
作者
Aletti, Anna B. [1 ,2 ]
Blasco, Salvador [1 ,2 ,3 ]
Aramballi, Savyasachi J. [1 ,2 ]
Kruger, Paul E. [4 ]
Gunnlaugsson, Thorfinnur [1 ,2 ]
机构
[1] Univ Dublin, Trinity Coll Dublin, Sch Chem, Dublin 2, Ireland
[2] Univ Dublin, Trinity Coll Dublin, AMBER Adv Mat & BioEngn Res Ctr, Dublin 2, Ireland
[3] Univ Valencia, Dept Quim Inorgan, Inst Ciencia Mol, Inorgan, Edificio Inst Paterna, Valencia 46980, Spain
[4] Univ Canterbury, Sch Phys & Chem Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Private Bag 4800, Christchurch 8041, New Zealand
基金
爱尔兰科学基金会;
关键词
PROTONATION CONSTANTS; RECOGNITION; BINDING; CAGE; GELS; NMR;
D O I
10.1016/j.chempr.2019.06.023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using solution and solid-state analyses, we demonstrate that the tripodal N-methylated(1,3,5-benzene-tricarboxamide)-tris(phenylurea) BTA ligands, possessing urea functionalities in the meta position, are able to form extended self-assembly 2D networks via hydrogen bonding templated by sulfate (SO42-). The divergence of the urea binding sites confers a propeller-like conformation to the ligands and is key to formation of the self-assemblies. Studies in solution and in the solid state as well as scanning electron microscopy (SEM) on the self-assembly properties of the ligands showed that the convergence also leads to the formation of hierarchical structures, including porous films and spherical nano-sized particles; the morphological outcome is highly solvent dependent.
引用
收藏
页码:2617 / 2629
页数:13
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