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X-ray spectroscopy characterization of self-assembled monolayers of nitrile-substituted oligo(phenylene ethynylene)s with variable chain length

机译:可变链长的腈取代的低聚(亚苯基乙炔基)自组装单层的X射线光谱表征

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摘要

Self-assembled monolayers (SAMs) of nitrile-substituted oligo(phenylene ethynylene) thiols (NC-OPEn) with a variable chain length n (n ranging from one to three structural units) on Au(111) were studied by synchrotron-based high-resolution X-ray photoelectron spectroscopy and near-edge absorption fine-structure spectroscopy. The experimental data suggest that the NC-OPEn molecules form well-defined SAMs on Au(111), with all the molecules bound to the substrate through the gold–thiolate anchor and the nitrile tail groups located at the SAM–ambient interface. The packing density in these SAMs was found to be close to that of alkanethiolate monolayers on Au(111), independent of the chain length. Similar behavior was found for the molecular inclination, with an average tilt angle of ~33–36° for all the target systems. In contrast, the average twist of the OPEn backbone (planar conformation) was found to depend on the molecular length, being close to 45° for the films comprising the short OPE chains and ~53.5° for the long chains. Analysis of the data suggests that the attachment of the nitrile moiety, which served as a spectroscopic marker group, to the OPEn backbone did not significantly affect the molecular orientation in the SAMs.
机译:通过基于同步加速器的高电子学研究了在Au(111)上具有可变链长n(n为1至3个结构单元)的腈取代的低聚(亚苯基亚乙炔基)硫醇(NC-OPEn)的自组装单层(SAMs)分辨率X射线光电子能谱和近边缘吸收精细结构能谱。实验数据表明,NC-OPEn分子在Au(111)上形成了明确定义的SAM,所有分子均通过硫醇金锚定分子和位于SAM-环境界面的腈尾基团与底物结合。发现这些SAM中的堆积密度接近于Au(111)上链烷硫醇单分子层的堆积密度,与链长无关。对于分子倾斜也发现了类似的行为,所有目标系统的平均倾斜角约为33–36°。相反,发现OPEn主链的平均扭曲(平面构象)取决于分子长度,对于包含短OPE链的膜而言,其接近45°,对于长链膜而言,其约为53.5°。数据分析表明,用作光谱标记基团的腈部分与OPEn主链的连接不会显着影响SAM中的分子方向。

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