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首页> 外文期刊>The Journal of Chemical Physics >Self-assembly and conformation of tetrapyridyl-porphyrin molecules on Ag(111)
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Self-assembly and conformation of tetrapyridyl-porphyrin molecules on Ag(111)

机译:四吡啶基卟啉分子在Ag(111)上的自组装和构象

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We present a low-temperature scanning tunneling microscopy (STM) study on the supramolecular ordering of tetrapyridyl-porphyrin (TPyP) molecules on Ag(111). Vapor deposition in a wide substrate temperature range reveals that TPyP molecules easily diffuse and self-assemble into large, highly ordered chiral domains. We identify two mirror-symmetric unit cells, each containing two differently oriented molecules. From an analysis of the respective arrangement it is concluded that lateral intermolecular interactions control the packing of the layer, while its orientation is induced by the coupling to the substrate. This finding is corroborated by molecular mechanics calculations. High-resolution STM images recorded at 15 K allow a direct identification of intramolecular features. This makes it possible to determine the molecular conformation of TPyP on Ag(111). The pyridyl groups are alternately rotated out of the porphyrin plane by an angle of 60 degrees. (c) 2006 American Institute of Physics.
机译:我们提出了对Ag(111)上的四吡啶基卟啉(TPyP)分子的超分子排序的低温扫描隧道显微镜(STM)研究。在较宽的底物温度范围内气相沉积表明TPyP分子易于扩散并自组装成大的,高度有序的手性域。我们确定了两个镜像对称的晶胞,每个晶胞包含两个不同取向的分子。从对各个布置的分析可以得出结论,横向分子间相互作用控制该层的堆积,而其取向是通过与基底的偶联而诱导的。分子力学计算证实了这一发现。以15 K记录的高分辨率STM图像可直接识别分子内特征。这使得有可能确定TPyP在Ag(111)上的分子构象。吡啶基交替地从卟啉平面旋转60度角。 (c)2006年美国物理研究所。

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