Barlow Susan M, Louafi Souheila, Le Roux Delphine, Williams Jamie, Muryn Christopher, Haq Sam, Raval Rasmita
Surface Science Research Centre, University of Liverpool, Liverpool, L69 3BX, United Kingdom.
Langmuir. 2004 Aug 17;20(17):7171-6. doi: 10.1021/la049391b.
The bonding and self-assembly of a chirally organized monolayer of alanine on the Cu(110) surface has been investigated using reflection-absorption infrared spectroscopy, low-energy electron diffraction (LEED), and scanning tunneling microscopy (STM). This multitechnique approach has enabled an in-depth understanding of the hierarchy of chirality transfer: from a single adsorbed molecule, to size-defined chiral clusters, and then to an overall chiral assembly. The data have indicated that the alanine is in its anionic form, bound to the copper surface through the oxygens of the ionized carboxylate group and the nitrogen of the neutral amino group. Importantly, the methyl group is held away from the surface, resulting in direct chirality transfer into the footprint of the adsorbed alanine molecules, with the local adsorption motif for S-alanine being the mirror image of that created for R-alanine. STM has shown that S-alanine molecules self-organize to form size-defined chiral clusters of six or eight molecules at the surface, interspersed with chiral channels of bare metal. Together, these clusters and channels further self-assemble into a chiral array with one unique chiral domain sustained across the entire surface. A similar chiral assembly, but with the mirror organization, has been observed for R-alanine. Structural models for the individual clusters are proposed, and in conjunction with LEED data, overall models for these chiral phases of both S- and R-alanine have been constructed. Overall, this adsorption system has been found to be both strongly chemisorbed and capable of extensive intermolecular H-bonding, causing stresses that lead not only to the chiral self-organization of molecules but also to a specific self-organization of the empty chiral channels and spaces that intersperse the structure which, in turn, chirally assemble across macroscopic length scales to give a surface with global organizational chirality.
利用反射吸收红外光谱、低能电子衍射(LEED)和扫描隧道显微镜(STM)研究了丙氨酸在Cu(110)表面的手性组织单层的键合和自组装。这种多技术方法能够深入理解手性转移的层次结构:从单个吸附分子到尺寸确定的手性簇,再到整体手性组装。数据表明,丙氨酸呈阴离子形式,通过离子化羧基的氧和中性氨基的氮与铜表面结合。重要的是,甲基远离表面,导致手性直接转移到吸附的丙氨酸分子的足迹中,S-丙氨酸的局部吸附模式是R-丙氨酸所形成模式的镜像。STM表明,S-丙氨酸分子在表面自组织形成由六个或八个分子组成的尺寸确定的手性簇,其间穿插着裸金属的手性通道。这些簇和通道一起进一步自组装成手性阵列,在整个表面上维持一个独特的手性域。对于R-丙氨酸,观察到了类似的手性组装,但具有镜像结构。提出了单个簇的结构模型,并结合LEED数据,构建了S-和R-丙氨酸这些手性相的整体模型。总体而言,已发现该吸附系统既具有强烈的化学吸附作用,又能够进行广泛的分子间氢键作用,从而产生应力,不仅导致分子的手性自组织,还导致空的手性通道和穿插在结构中的空间的特定自组织,这些通道和空间又在宏观长度尺度上手性组装,形成具有全局组织手性的表面。