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Impact of the Schiff base ligand substituents on the solid state and solution properties of eleven iron(iii) complexes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F19%3A73598089" target="_blank" >RIV/61989592:15310/19:73598089 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlehtml/2019/nj/c9nj03087e" target="_blank" >https://pubs.rsc.org/en/content/articlehtml/2019/nj/c9nj03087e</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c9nj03087e" target="_blank" >10.1039/c9nj03087e</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Impact of the Schiff base ligand substituents on the solid state and solution properties of eleven iron(iii) complexes

  • Original language description

    Investigations on a series of mononuclear iron(iii) Schiff base complexes of the general formula [Fe(L)Cl]center dot S (where L2- is a Schiff base ligand anion, S is a solvent molecule) are reported. Derivatives of salicylaldehyde or 2-hydroxy-1-naphthaldehyde were used in combination with linear either symmetrical or non-symmetrical aliphatic triamines to synthesize the Schiff base ligands and subsequent reactions with iron(iii) chloride afforded various [Fe(L)Cl] complexes. Compounds were characterized by conventional techniques and the crystal structures of all complexes were determined as well. A structural study revealed the relationship between the spatial arrangement of the N3O2-donor atom set and the length of the aliphatic part of the Schiff base ligand. Magnetic and EPR investigations confirmed the high spin state behaviour in all reported compounds and their analysis allowed quantification of the spin Hamiltonian parameters. Formation of hydrogen-bonded pseudodimers with an antiferromagnetic exchange coupling was found in the complexes with the shortest aliphatic part of the Schiff base ligands. Experimental exchange coupling constants were in good agreement with those obtained from DFT calculations and correlated with the strength of the hydrogen bonds. Cyclic and square wave voltammetry techniques were employed to investigate the redox properties of the reported compounds and the experimental redox potentials were compared with those obtained from the DFT calculations.

  • 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/LO1305" target="_blank" >LO1305: Development of the center of advanced technologies and materials</a><br>

  • Continuities

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

Others

  • Publication year

    2019

  • 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

  • Volume of the periodical

    43

  • Issue of the periodical within the volume

    35

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    13

  • Pages from-to

    13916-13928

  • UT code for WoS article

    000484979300024

  • EID of the result in the Scopus database

    2-s2.0-85072103043