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STM study of terephthalic acid self-assembly on Au(111): Hydrogen-bonded sheets on an inhomogeneous substrate

机译:对苯二甲酸在Au(111)上的自组装的STM研究:非均质基材上的氢键合板

摘要

The adsorption and ordering of the molecule terephthalic acid (TPA), 1,4-benzene-dicarboxylic acid C6H4-(COOH)(2), on the reconstructed Au(111) surface has been studied in situ in ultrahigh vacuum by scanning tunneling microscopy (STM) at room temperature. Two-dimensional (2D) self-assembled supramolecular domains evolve, wherein the well-known one-dimensional (1D) carboxyl H-bond pairing scheme is identified. Since the individual molecules occupy a distinct adsorption site and the supramolecular ordering usually extends over several substrate reconstruction domains, a significant variation in hydrogen bond lengths is encountered, which illustrates the versatility of hydrogen bridges in molecular engineering at surfaces. Ab initio calculations for a 1D H-bonded molecular chain provide insight into the limited geometric response of the molecules in different local environments.
机译:通过扫描隧道显微镜在超高真空下原位研究了分子对苯二甲酸(TPA)1,4,4-苯二甲酸C6H4-(COOH)(2)的吸附和有序化。 (STM)在室温下。二维(2D)自组装超分子域不断发展,其中确定了众所周知的一维(1D)羧基H键配对方案。由于各个分子占据一个独特的吸附位点,并且超分子顺序通常会延伸到几个底物重建域上,因此会遇到氢键长度的显着变化,这说明了氢键在表面分子工程中的多功能性。一维氢键分子链的从头算计算可洞悉不同局部环境中分子的有限几何响应。

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