Effect of Coordination Geometry on Magnetic Properties in a Series of Cobalt(II) Complexes and Structural Transformation in Mother Liquor

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F20%3A73603256" target="_blank" >RIV/61989592:15310/20:73603256 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216305:26620/20:PU137426

Výsledek na webu

<a href="https://pubs.acs.org/doi/10.1021/acs.inorgchem.0c00538" target="_blank" >https://pubs.acs.org/doi/10.1021/acs.inorgchem.0c00538</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acs.inorgchem.0c00538" target="_blank" >10.1021/acs.inorgchem.0c00538</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Effect of Coordination Geometry on Magnetic Properties in a Series of Cobalt(II) Complexes and Structural Transformation in Mother Liquor

Popis výsledku v původním jazyce

The three Co(II) complexes [Co(bbp)(2)][Co(NCS)(4)]center dot 4DMF (1), [Co(bbp)(NCS)2(DMF)]center dot 2DMF (2), and [Co(bbp)(NCS)(2)] (3) have been synthesized and characterized by single-crystal X-ray diffraction, magnetic, and various spectroscopic techniques. Complexes 1 and 3 are obtained by the reaction of Co(NCS) 2 with 2,6-bis(1H-benzo[d]imidazol-2-yl)pyridine (bbp), and complex 1 undergoes a structural transformation to form complex 2. A single-crystal X-ray study revealed that complex 1 is comprised of two Co(II) centers, a cationic octahedral Co(II) unit and an anionic tetrahedral Co(II) unit, while the Co(II) ion is in a distorted-octahedral environment in 2. Moreover, in complex 3, the Co(II) ion is in a distorted-square-pyramidal geometry. The effect of coordination geometry on the magnetic properties was studied by both static and dynamic magnetic measurements. Direct current (dc) magnetic susceptibility measurements showed that all of the Co(II) ions are in high-spin state in these complexes. Alternating current (ac) magnetic susceptibility measurements indicated that complexes 2 and 3 display slow relaxation of magnetization in an external dc magnetic field, while complex 1 displayed no such property. EPR experiments and theoretical calculations were consistent with the above findings.

Název v anglickém jazyce

Effect of Coordination Geometry on Magnetic Properties in a Series of Cobalt(II) Complexes and Structural Transformation in Mother Liquor

Popis výsledku anglicky

The three Co(II) complexes [Co(bbp)(2)][Co(NCS)(4)]center dot 4DMF (1), [Co(bbp)(NCS)2(DMF)]center dot 2DMF (2), and [Co(bbp)(NCS)(2)] (3) have been synthesized and characterized by single-crystal X-ray diffraction, magnetic, and various spectroscopic techniques. Complexes 1 and 3 are obtained by the reaction of Co(NCS) 2 with 2,6-bis(1H-benzo[d]imidazol-2-yl)pyridine (bbp), and complex 1 undergoes a structural transformation to form complex 2. A single-crystal X-ray study revealed that complex 1 is comprised of two Co(II) centers, a cationic octahedral Co(II) unit and an anionic tetrahedral Co(II) unit, while the Co(II) ion is in a distorted-octahedral environment in 2. Moreover, in complex 3, the Co(II) ion is in a distorted-square-pyramidal geometry. The effect of coordination geometry on the magnetic properties was studied by both static and dynamic magnetic measurements. Direct current (dc) magnetic susceptibility measurements showed that all of the Co(II) ions are in high-spin state in these complexes. Alternating current (ac) magnetic susceptibility measurements indicated that complexes 2 and 3 display slow relaxation of magnetization in an external dc magnetic field, while complex 1 displayed no such property. EPR experiments and theoretical calculations were consistent with the above findings.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

<a href="/cs/project/LQ1601" target="_blank" >LQ1601: CEITEC 2020</a><br>

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2020

Kód důvěrnosti údajů

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

Název periodika

INORGANIC CHEMISTRY

ISSN

0020-1669

e-ISSN

—

Svazek periodika

59

Číslo periodika v rámci svazku

10

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

15

Strana od-do

7067-7081

Kód UT WoS článku

000535304900041

EID výsledku v databázi Scopus

2-s2.0-85084581585