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Coexistence of one- and two-dimensional supramolecular assemblies of terephthalic acid on Pd(111) due to self-limiting deprotonation

  • M. E. Cañas-Ventura
  • , F. Klappenberger
  • , S. Clair
  • , S. Pons
  • , K. Kern
  • , H. Brune
  • , T. Strunskus
  • , Ch Wöll
  • , R. Fasel
  • , J. V. Barth
  • École Polytechnique Fédérale de Lausanne (EPFL)
  • Laboratory for Functional Polymers
  • Institute of Physical and Chemical Research (RIKEN)
  • LORIA, UMR 7503, University of Lorraine
  • Max Planck Institute for Solid State Research
  • Max-Planck-lnstitut für Kohlenforschung
  • University of British Columbia

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

The adsorption of terephthalic acid [C6 H4 (COOH)2, TPA] on a Pd(111) surface has been investigated by means of scanning tunneling microscopy (STM), x-ray photoelectron spectroscopy, and near-edge x-ray absorption fine structure spectroscopy under ultrahigh vacuum conditions at room temperature. We find the coexistence of one- (1D) and two-dimensional (2D) molecular ordering. Our analysis indicates that the 1D phase consists of intact TPA chains stabilized by a dimerization of the self-complementary carboxyl groups, whereas in the 2D phase, consisting of deprotonated entities, the molecules form lateral ionic hydrogen bonds. The supramolecular growth dynamics and the resulting structures are explained by a self-limiting deprotonation process mediated by the catalytic activity of the Pd surface. Our models for the molecular ordering are supported by molecular mechanics calculations and a simulation of high resolution STM images.

Original languageEnglish
Article number184710
JournalJournal of Chemical Physics
Volume125
Issue number18
DOIs
StatePublished - 2006
Externally publishedYes

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