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Bonding Motifs in Metal-Organic Compounds on Surfaces

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F18%3A73591469" target="_blank" >RIV/61989592:15310/18:73591469 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378271:_____/18:00501415

  • Result on the web

    <a href="https://pubs.acs.org/doi/10.1021/jacs.8b06765" target="_blank" >https://pubs.acs.org/doi/10.1021/jacs.8b06765</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/jacs.8b06765" target="_blank" >10.1021/jacs.8b06765</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Bonding Motifs in Metal-Organic Compounds on Surfaces

  • Original language description

    The bonds in metal organic networks on surfaces govern the resulting geometry as well as the electronic properties. Here, we study the nature of these bonds by forming phenazine-copper complexes on a copper surface by means of atomic manipulation. The structures are characterized by a combination of scanning probe microscopy and density functional theory calculations. We observed an increase of the molecule-substrate distance upon covalent bond formation and an out-of-plane geometry that is in direct contradiction with the common expectation that these networks are steered by coordination bonds. Instead, we find that a complex energy balance of hybridization with the substrate, inhomogeneous Pauli repulsion, and elastic deformation drives the phenazine-copper interaction. Most remarkably, this attractive interaction is not driven by electron acceptor properties of copper but is of completely different donation/back-donation mechanism between molecular pi-like orbitals and sp-like metal states. Our findings show that the nature of bonds between constituents adsorbed on surfaces does not have to follow the common categories.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

  • ISSN

    0002-7863

  • e-ISSN

  • Volume of the periodical

    140

  • Issue of the periodical within the volume

    40

  • Country of publishing house

    AF - AFGHANISTAN

  • Number of pages

    6

  • Pages from-to

    12884-12889

  • UT code for WoS article

    000447354800038

  • EID of the result in the Scopus database

    2-s2.0-85054357687