Chemisorption of ferrocene on Si(111)-Ag√3: Frustrated conformational flexibility

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Original languageEnglish
Pages (from-to)267-271
Number of pages5
JournalSurface Science
Volume605
Issue number3-4
Publication statusPublished - 22 Oct 2010

Abstract

The adsorption of ferrocene-dithiol on Si(111)-Ag√3× √3 reconstruction has been studied by scanning tunneling microscopy. Preferred chemisorption was found at defect sites, e.g. grain boundaries, with characteristic distortions of the two dimensional electron gas. Occasionally, adsorption also occurs at perfect terrace sites, where submolecular resolution was achieved and the adsorption geometry was deduced. Due to the formation of Ag-S bonds, the conformational flexibility of the free ferrocene is restricted. Thus, the frozen rotation leaves only two different rotational configurations of ferrocene.

Keywords

    Hybrid interface, Molecules, STM

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Chemisorption of ferrocene on Si(111)-Ag√3: Frustrated conformational flexibility. / Tegenkamp, Christoph; Schmeidel, Jedrzej; Pfnür, Herbert.
In: Surface Science, Vol. 605, No. 3-4, 22.10.2010, p. 267-271.

Research output: Contribution to journalArticleResearchpeer review

Tegenkamp C, Schmeidel J, Pfnür H. Chemisorption of ferrocene on Si(111)-Ag√3: Frustrated conformational flexibility. Surface Science. 2010 Oct 22;605(3-4):267-271. doi: 10.1016/j.susc.2010.10.027
Tegenkamp, Christoph ; Schmeidel, Jedrzej ; Pfnür, Herbert. / Chemisorption of ferrocene on Si(111)-Ag√3 : Frustrated conformational flexibility. In: Surface Science. 2010 ; Vol. 605, No. 3-4. pp. 267-271.
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abstract = "The adsorption of ferrocene-dithiol on Si(111)-Ag√3× √3 reconstruction has been studied by scanning tunneling microscopy. Preferred chemisorption was found at defect sites, e.g. grain boundaries, with characteristic distortions of the two dimensional electron gas. Occasionally, adsorption also occurs at perfect terrace sites, where submolecular resolution was achieved and the adsorption geometry was deduced. Due to the formation of Ag-S bonds, the conformational flexibility of the free ferrocene is restricted. Thus, the frozen rotation leaves only two different rotational configurations of ferrocene.",
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T2 - Frustrated conformational flexibility

AU - Tegenkamp, Christoph

AU - Schmeidel, Jedrzej

AU - Pfnür, Herbert

N1 - Funding information: We thank Ingmar Baumgardt and Holger Butenschön from the organic chemistry department in Hannover for functionalization of ferrocene molecules with thiol groups. The work was financially supported by the Deutsche Forschungsgemeinschaft .

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