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Probing Conformer and Adsorption Footprint Distributions at the Single-Molecule Level in a Highly Organised Amino-Acid Assembly of (S)-Proline on Cu(110)

M. Forster ; M. S. Dyer ; Mats Persson (Institutionen för teknisk fysik, Material- och ytteori) ; R Raval
Journal of American Chemical Society (0002-7863). Vol. 131 (2009), 29, p. 10173.
[Artikel, refereegranskad vetenskaplig]

Establishing the nanoscale details of organized amino acid assemblies at surfaces is a major challenge in the field of organic-inorganic interfaces. Here, we show that the dense (4 x 2) overlayer of the amino acid, (S)-proline on a Cu(110) surface can be explored at the single-molecule level by scanning tunneling microscopy (STM), reflection absorption infrared spectroscopy (RAIRS), and periodic density functional theory (DFT) calculations. The combination of experiment and theory, allied with the unique structural rigidity of proline, enables the individual conformers and adsorption footprints adopted within the organized assembly to be determined. Periodic DFT calculations find two energetically favorable molecular conformations, projecting mirror-image chiral adsorption footprints at the surface. These two forms can be experimentally distinguished since the positioning of the amino group within the pyrrolidine ring leads each chiral footprint and associated conformer to adopt very different ring orientations, producing distinct contrasts in the STM images. DFT modeling shows that the two conformers can generate eight possible (4 x 2) overlayers with a variety of adsorption footprint arrangements. STM images simulated for each structural model enables a direct comparison to be made with the experiment and narrows the (4 x 2) overlayer to one specific structural model in which the juxtaposition of molecules leads to the formation of one-dimensional hydrogen bonded prolate chains directed along the [1 (1) over bar0] direction.

Denna post skapades 2009-12-26. Senast ändrad 2013-10-29.
CPL Pubid: 104902


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