堆积
氢键
化学
超分子化学
共价键
超分子聚合物
结晶学
聚合物
分子间力
侧链
分子
有机化学
晶体结构
作者
Luc Brunsveld,J.A.J.M. Vekemans,J. H. K. Ky Hirschberg,Rint P. Sijbesma,E. W. Meijer
标识
DOI:10.1073/pnas.072659099
摘要
Bifunctional ureido- s -triazines provided with penta(ethylene oxide) side chains are able to self assemble in water, leading to helical columns via cooperative stacking of the hydrogen-bonded pairs (DADA array). Monofunctional ureido- s -triazines do not form such helical architectures. The presence of a linker, covalently connecting the two ureido- s -triazine units, is essential as it generates a high local concentration of aromatic units, favorable for stacking interactions. This hydrophobic stacking of the aromatic units occurs at concentrations as low as 5⋅10 −6 M and can be visualized by using fluorescence spectroscopy. The stacking generates a hydrophobic microenvironment that allows intermolecular hydrogen bonding to occur at higher concentrations because the hydrogen bonds are shielded from competitive hydrogen bonding with water. This hierarchical process results in the formation of a helical self-assembled polymer in water at concentrations above 10 −4 M. Chiral side chains attached to the ureido- s -triazine units bias the helicity of these columns as concluded from CD spectroscopy and “Sergeants and Soldiers” experiments.
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