Fabrication of a Complex Two-Dimensional Adenine-Perylene-3,4,9, 10-tetracarboxylic Dianhydride Chiral Nanoarchitecture through Molecular Self-Assembly

Xiaonan Sun, Manuela Mura, Harry T. Jonkman, Lev N. Kantorovich*, Fabien Silly

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

The two-dimensional self-assembly of a nonsyrnmetric adenine DNA base mixed with symmetric perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA) molecules is investigated using scanning tunneling microscopy (STM). We experimentally observe that these two building blocks form a complex close-packed chiral supramolecular network on Au(111). The unit cell of the adenine PTCDA nanoarchitecture is composed of 14 molecules. The high stability of this structure relies on PTCDA-PTCDA and PTCDA-adenine hydrogen bonding. Detailed theoretical analysis based on the density functional theory (DFT) calculations reveals that adenine molecules work as a "glue", providing additional strengthening to the PTCDA-based skeleton of this sophisticated multicomponent nanoarchitecture. At the same time, we find that orientation and chirality of adenine molecules across the monolayer is likely to vary, leading to a disorder in the atomistic structure of the entire assembly.

Original languageEnglish
Pages (from-to)2493-2499
Number of pages7
JournalJournal of Physical Chemistry C
Volume116
Issue number3
DOIs
Publication statusPublished - 26-Jan-2012

Keywords

  • DENSITY-FUNCTIONAL THEORY
  • HOMOPAIRING POSSIBILITIES
  • SUPRAMOLECULAR NETWORKS
  • MELAMINE
  • SURFACE
  • DNA
  • AU(111)
  • DIMENSIONS
  • URACIL
  • ROBUST

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