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Dehydrocyclization of peripheral alkyl groups in porphyrins at Cu(100) and Ag(111) surfaces

机译:Cu(100)和Ag(111)表面卟啉中外围烷基的脱氢环化

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The self-assembly of organic and metal-organic species at metal surfaces is a topic of high interest for applications that can benefit from tunable surface functionalization through, organic:building block design. As the complexity of molecular building blocks increases to direct ordering and function, thermal stability of the adsorbate often increases opening up new surface-catalyzed reaction pathways. We report dehydrocyclization of octaethylporphyrin to tetrabenzoporphyrin on the Cu(100) and Ag(111) surfaces at 500-600 K. Dehydrocyclization of smaller species is not typically observed on these surfaces at low pressure due to short adsorption lifetimes. The dehydrocyclization of peripheral ethyl groups forms benzo groups which then undergo additional dehydrogenation. The reaction products are characterized by high resolution electron energy loss spectroscopy (HREELS), scanning tunneling microscopy (STM), and X-ray photoelectron spectroscopy (XPS). These results extend our understanding of reaction pathways that may be encountered as molecular building blocks increase in size and complexity on relatively inert surfaces. (C) 2016 Elsevier B.V. All rights reserved.
机译:有机和金属有机物种在金属表面的自组装是应用的一个高度关注的话题,这些应用可以通过有机:构件设计而受益于可调整的表面功能化。随着分子结构单元的复杂性增加以指导有序和功能的发展,被吸附物的热稳定性通常会增加开放新的表面催化反应路径的机会。我们报告在500-600 K在铜(100)和银(111)表面上的八乙基卟啉脱氢环化为四苯并卟啉。较小的物种通常在低压下由于短的吸附寿命而未观察到较小物种的脱氢环化。外围乙基的脱氢环化形成苯并基,然后进行额外的脱氢。反应产物的特征在于高分辨率电子能量损失谱(HREELS),扫描隧道显微镜(STM)和X射线光电子能谱(XPS)。这些结果扩展了我们对在相对惰性表面上分子构造单元的尺寸和复杂性增加时可能遇到的反应途径的理解。 (C)2016 Elsevier B.V.保留所有权利。

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