Cazacu Adinela, Tong Christine, van der Lee Arie, Fyles Thomas M, Barboiu Mihail
Institut Européen des Membranes--UMR-CNRS 5635, Place Eugène Bataillon, CC 047, F-34095 Montpellier, Cedex 5, France.
J Am Chem Soc. 2006 Jul 26;128(29):9541-8. doi: 10.1021/ja061861w.
The self-assembly of ureido crown-ether derivatives has been examined in homogeneous solution, in the solid state, and in planar bilayer membranes. The self-assembly is driven by head-to-tail hydrogen bonding between the urea functional groups. Dimers and higher oligomers are formed in CDCl3 solution as assessed by the change in the ureido NH chemical shift as a function of concentration. Single-crystal X-ray diffraction shows that an antiparallel association of the ureas produces columnar channels composed of face-to-face crown ethers. Powder X-ray diffraction studies also show the presence of a minor phase based upon a parallel urea association leading to an alternative columnar arrangement of the crown ethers. In bilayer membranes at low concentration of ureido crown ether added, membrane disruption is observed together with rare single-channel openings, but at higher concentration, a rich array of interconverting channel conductance states is observed. The channel results are interpreted as arising from discreet stacks of ureido crown ethers where the transport of cations would occur via the macrocycles, admixed with larger pores formed by association of the crown ether headgroups around a central large pore.
已在均相溶液、固态和平面双层膜中研究了脲基冠醚衍生物的自组装。自组装由脲官能团之间的头对尾氢键驱动。通过脲基NH化学位移随浓度的变化评估,在CDCl₃溶液中形成了二聚体和更高的低聚物。单晶X射线衍射表明,脲的反平行缔合产生了由面对面的冠醚组成的柱状通道。粉末X射线衍射研究还表明,基于平行脲缔合存在一个次要相,导致冠醚的另一种柱状排列。在添加低浓度脲基冠醚的双层膜中,观察到膜破坏以及罕见的单通道开放,但在较高浓度下,观察到一系列丰富的相互转换的通道电导状态。通道结果被解释为来自脲基冠醚的离散堆叠,其中阳离子的运输将通过大环发生,并与由围绕中心大孔的冠醚头基缔合形成的较大孔混合。