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Multicolor photoluminescence of Cu14 clusters modulated using surface ligands

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F24%3A00588530" target="_blank" >RIV/61388980:_____/24:00588530 - isvavai.cz</a>

  • Result on the web

    <a href="https://hdl.handle.net/11104/0355578" target="_blank" >https://hdl.handle.net/11104/0355578</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d4sc01566e" target="_blank" >10.1039/d4sc01566e</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Multicolor photoluminescence of Cu14 clusters modulated using surface ligands

  • Original language description

    Copper nanoclusters exhibit unique structural features and their molecular assembly results in diverse photoluminescence properties. In this study, we present ligand-dependent multicolor luminescence observed in a Cu-14 cluster, primarily protected by ortho-carborane-9,12-dithiol (o-CBDT), featuring an octahedral Cu-6 inner kernel enveloped by eight isolated copper atoms. The outer layer of the metal kernel consists of six bidentate o-CBDT ligands, in which carborane backbones are connected through mu(3)-sulphide linkages. The initially prepared Cu-14 cluster, solely protected by six o-CBDT ligands, did not crystallize in its native form. However, in the presence of N,N-dimethylformamide (DMF), the cluster crystallized along with six DMF molecules. Single-crystal X-ray diffraction (SCXRD) revealed that the DMF molecules were directly coordinated to six of the eight capping Cu atoms, while oxygen atoms were bound to the two remaining Cu apices in antipodal positions. Efficient tailoring of the cluster surface with DMF shifted its luminescence from yellow to bright red. Luminescence decay profiles showed fluorescence emission for these clusters, originating from the singlet states. Additionally, we synthesized microcrystalline fibers with a one-dimensional assembly of DMF-appended Cu-14 clusters and bidentate DPPE linkers. These fibers exhibited bright greenish-yellow phosphorescence emission, originating from the triplet state, indicating the drastic surface tailoring effect of secondary ligands. Theoretical calculations provided insights into the electronic energy levels and associated electronic transitions for these clusters. This work demonstrated dynamic tuning of the emissive excited states of copper nanoclusters through the efficient engineering of ligands.

  • 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

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    <a href="/en/project/LTAIN19152" target="_blank" >LTAIN19152: Carborane-protected metal nanoclusters: A new family of materials with atomic precision</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Chemical Science

  • ISSN

    2041-6520

  • e-ISSN

    2041-6539

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    34

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    13741-13752

  • UT code for WoS article

    001283026100001

  • EID of the result in the Scopus database

    2-s2.0-85200385716