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The distinguishing effect of the magnetic states of cobalt on the performance of single-molecule magnet behaviors in closely related CoIIIDyIII and CoIIDyIII complexes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F24%3A73627719" target="_blank" >RIV/61989592:15310/24:73627719 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03979c" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03979c</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d4nj03979c" target="_blank" >10.1039/d4nj03979c</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The distinguishing effect of the magnetic states of cobalt on the performance of single-molecule magnet behaviors in closely related CoIIIDyIII and CoIIDyIII complexes

  • Original language description

    This report details the synthesis and characterization of heterobimetallic 3d-4f complexes, labeled as 1 and 2, utilizing a new Schiff base ligand derived from the condensation of 2-aminobenzyl alcohol with a methyl-substituted o-vanillin. A comprehensive structural analysis reveals that complex 1 comprises a CoIII-DyIII assembly, bridged by two alkoxide groups, in which the CoIII center adopts an octahedral geometry, and the DyIII ion is situated within a DyO9 coordination sphere. Under nearly identical reaction conditions, an intramolecular nucleophilic attack led to a subtle modification of approximately one-half of the ligand from H2L to HL &apos;, resulting in the isolation of complex 2. This complex features a CoII-DyIII core, bridged by a pivalate ion along with phenoxide groups. To the best of our knowledge, this is a rare instance of dinuclear Co-Dy systems exhibiting variable oxidation states of the cobalt center within a similar ligand framework. Both complexes 1 and 2 exhibit field-induced slow relaxation of magnetization, and theoretical analysis revealed that in complex 1, the principal magnetic axis aligns with the shortest Dy-O bond, underscoring the charge polarization effect exerted by the diamagnetic CoIII ion in tuning the crystal field around the DyIII ion, thereby influencing its magnetic anisotropy. Conversely, in complex 2, the ferromagnetic interaction between the CoII and DyIII ions significantly reduces quantum tunneling of magnetization (QTM). Additionally, we employed quantum theory of atoms in molecules (QT-AIM) calculations to investigate the nature of the coordination bonds in these 3d-4f complexes, which provided insights into the crystal field strength around the LnIII ions and their subsequent magnetic anisotropy. This study broadens the exploration of Schiff base-derived 3d-4f complexes and their magnetic properties, highlighting the potential for further advancements in this field.

  • 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

    <a href="/en/project/GA23-07175S" target="_blank" >GA23-07175S: Semicoordination: a route to chemically stable molecular nanomagnets</a><br>

  • Continuities

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

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

    NEW JOURNAL OF CHEMISTRY

  • ISSN

    1144-0546

  • e-ISSN

    1369-9261

  • Volume of the periodical

    48

  • Issue of the periodical within the volume

    48

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    13

  • Pages from-to

    20410-20422

  • UT code for WoS article

    001364000600001

  • EID of the result in the Scopus database

    2-s2.0-85210927018