Kim Moonhee, Hohman J Nathan, Morin Elizabeth I, Daniel Thomas A, Weiss Paul S
Department of Chemistry and Physics, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
J Phys Chem A. 2009 Apr 23;113(16):3895-903. doi: 10.1021/jp810048n.
We have investigated the formation of 2-adamantanethiolate self-assembled monolayers on Au{111} and their displacement by n-dodecanethiol, using scanning tunneling microscopy, X-ray photoelectron spectroscopy, and infrared reflection absorption spectroscopy. Well-ordered 2-adamantanethiolate monolayers undergo rapid and significant molecular exchange upon exposure to n-dodecanethiol solutions, but their structures and intermolecular interactions template the growth of n-dodecanethiolate domains. Annealing 2-adamantanethiolate monolayers at 78 degrees C decreases the density of vacancy islands, while increasing the overall order and the average domain sizes in the films. This results in slower displacement by n-dodecanethiol molecules, as compared to unannealed monolayers. The secondary sulfur position on the adamantyl cage influences the lattice structure and exchange of 2-adamantanethiolate monolayers by alkanethiols.
我们利用扫描隧道显微镜、X射线光电子能谱和红外反射吸收光谱,研究了2-金刚烷硫醇盐自组装单分子层在Au{111}上的形成及其被正十二烷硫醇取代的过程。有序的2-金刚烷硫醇盐单分子层在暴露于正十二烷硫醇溶液时会发生快速且显著的分子交换,但其结构和分子间相互作用为正十二烷硫醇盐域的生长提供了模板。在78摄氏度下对2-金刚烷硫醇盐单分子层进行退火处理,可降低空位岛的密度,同时提高薄膜的整体有序度和平均域尺寸。与未退火的单分子层相比,这导致正十二烷硫醇分子的取代速度变慢。金刚烷基笼上的二级硫位置会影响2-金刚烷硫醇盐单分子层被链烷硫醇取代时的晶格结构和交换情况。