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A combined experimental and theoretical study on a single, unsupported oxo-bridged Mn(iii,iii) dimer coordinated to two iminobenzosemiquinone π-radical anions

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F21%3A00543394" target="_blank" >RIV/61388963:_____/21:00543394 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15640/21:73611124

  • Result on the web

    <a href="https://doi.org/10.1039/D1DT00489A" target="_blank" >https://doi.org/10.1039/D1DT00489A</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d1dt00489a" target="_blank" >10.1039/d1dt00489a</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A combined experimental and theoretical study on a single, unsupported oxo-bridged Mn(iii,iii) dimer coordinated to two iminobenzosemiquinone π-radical anions

  • Original language description

    Ligand H2LAP comprises a non-innocent 2-aminophenol unit and an innocent bis(pyridin-2-ylmethyl)amine unit. The ligand, upon reaction with an equivalent amount of Mn(ClO4)2·6H2O in the presence of Et3N under air in MeOH, provided a mono(oxo)-bridged dinuclear Mn2 complex ({[(LISQ)MnIII–O–MnIII(LISQ)][(ClO4)]2}, 1). X-ray crystal structure analysis of complex 1 revealed that in the dicationic unit, the physical oxidation state of each Mn ion was +III and the 2-aminophenol unit of ligand H2LAP was in its one-electron oxidized iminobenzosemiquinone form. 1H-NMR measurement of complex 1 confirmed that the complex acquired a diamagnetic ground state (St = 0). Thus, antiferromagnetic couplings among the paramagnetic centers were realized. The UV-Vis-NIR spectrum of complex 1 was consisted of ligand-to-metal charge-transfer transitions in the visible region, while ligand-to-metal and metal-to-ligand charge-transfer transitions were noticed in the near-infrared region due to the presence of iminobenzosemiquinone radical units. The cyclic voltammogram of the complex showed three one-electron oxidation waves and two one-electron reduction waves. While the first two oxidation processes were metal-based, the two successive reductions were ligand-centered. DFT-based theoretical studies confirmed the assignment.

  • 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

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Dalton Transactions

  • ISSN

    1477-9226

  • e-ISSN

    1477-9234

  • Volume of the periodical

    50

  • Issue of the periodical within the volume

    25

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    8768-8775

  • UT code for WoS article

    000657790000001

  • EID of the result in the Scopus database

    2-s2.0-85108868156