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Two‑dimensional crystallization of pentagonal symmetric molecules

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F25%3A00644258" target="_blank" >RIV/68378271:_____/25:00644258 - isvavai.cz</a>

  • Result on the web

    <a href="https://hdl.handle.net/11104/0374107" target="_blank" >https://hdl.handle.net/11104/0374107</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11224-025-02584-6" target="_blank" >10.1007/s11224-025-02584-6</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Two‑dimensional crystallization of pentagonal symmetric molecules

  • Original language description

    Fivefold symmetry is incompatible with the translational periodicity of two-dimensional crystalline lattices. Nonetheless, aperiodic tilings, such as those introduced by Penrose and anticipated in Islamic geometric art, have demonstrated that local fivefold symmetry and long-range order can coexist without periodic repetition. Inspired by these mathematical constructs, recent advances in surface science have enabled the study of molecular self-assembly in two dimensions using molecules with intrinsic fivefold symmetry. In particular, penta-substituted derivatives of corannulene—rigid, bowl-shaped molecules resembling hard pentagons—exhibit intriguing self-assembly behavior on metal surfaces. Scanning tunneling microscopy (STM) reveals that these molecules organize into dense monolayers with stripe and rotator packing motifs reminiscent of theoretically predicted pentagonal tilings. Subtle variations in chirality and substitution patterns lead to diverse plane group symmetries (pm, p1, p2gg), domain boundaries, and packing densities. The balance between molecular geometry, chirality, and substrate interactions governs the emergence of ordered phases. These findings deepen our understanding of symmetry frustration, quasiperiodicity, and the transition between local and global order in molecular monolayers, with implications for the design of functional nanostructured materials.

  • 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

    10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Result continuities

  • Project

    <a href="/en/project/GA24-11064S" target="_blank" >GA24-11064S: Chirality-selective electron transport in single molecular devices</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Structural Chemistry

  • ISSN

    1040-0400

  • e-ISSN

    1572-9001

  • Volume of the periodical

    36

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    1973-1982

  • UT code for WoS article

    001550651400001

  • EID of the result in the Scopus database

    2-s2.0-105013559023