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Self-Assembled p-Carborane Analog of p-Mercaptobenzoic Acid on Au{111}

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F15%3A00445983" target="_blank" >RIV/61388955:_____/15:00445983 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378271:_____/15:00445983 RIV/61388980:_____/15:00445983

  • Result on the web

    <a href="http://dx.doi.org/10.1021/acs.chemmater.5b02263" target="_blank" >http://dx.doi.org/10.1021/acs.chemmater.5b02263</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.chemmater.5b02263" target="_blank" >10.1021/acs.chemmater.5b02263</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Self-Assembled p-Carborane Analog of p-Mercaptobenzoic Acid on Au{111}

  • Original language description

    The p-carborane cluster analog of p-mercaptobenzoic acid, 1-HS-12-COOH-1,12-C2B10H10, has been synthesized and characterized using nuclear magnetic resonance spectroscopy, single-crystal X-ray diffraction analysis, quantum- chemical calculations, and scanning tunneling microscopy. The single-crystal structure and selected packing aspects are discussed and presented in comparison with the two-dimensional periodic arrangements. Scanning tunneling micrographs, recorded under ambient conditions, are used to compare pure monolayers of 1-HS-1,12-C2B10H11 to co-adsorbed monolayers of both the parental precursor and carboxyl-functionalized p-carboranethiolate on Au{111}. Monolayers of both constituents are further characterized by X-ray photoelectron spectroscopy, which shows good agreement between the stoichiometry of each pure monolayer and the nominal stoichiometries of the respective molecules. Results indicate that most of the molecules of both derivatives adsorb as thiolates but that a small fraction of each adsorb as thiols, without complete SH bond scission, and consequently are labile relative to desorption. Wetting-angle measurements confirm the hydrophilic character of monolayers containing the carboxylic acid constituents. Mixed self-assembled monolayers with functionalized constituents of high axial symmetry provide a convenient basis for grafting two- and threedimensional structures.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CF - Physical chemistry and theoretical chemistry

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Chemistry of Materials

  • ISSN

    0897-4756

  • e-ISSN

  • Volume of the periodical

    27

  • Issue of the periodical within the volume

    15

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    5425-5435

  • UT code for WoS article

    000359499100033

  • EID of the result in the Scopus database

    2-s2.0-84938904576