2018
Hexanuclear iron(III) alpha-aminophosphonate: synthesis, structure, and magnetic properties of a molecular wheel
DOROSHENKO, Iaroslav, Michal BABIAK, Axel BUCHHOLZ, Jiří TUČEK, Winfried PLASS et. al.Základní údaje
Originální název
Hexanuclear iron(III) alpha-aminophosphonate: synthesis, structure, and magnetic properties of a molecular wheel
Autoři
DOROSHENKO, Iaroslav (804 Ukrajina, domácí), Michal BABIAK (703 Slovensko, domácí), Axel BUCHHOLZ (276 Německo), Jiří TUČEK (203 Česká republika), Winfried PLASS (276 Německo) a Jiří PINKAS (203 Česká republika, garant, domácí)
Vydání
New Journal of Chemistry, Cambridge, ROYAL SOC. CHEMISTRY, 2018, 1144-0546
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.069
Kód RIV
RIV/00216224:14310/18:00102320
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000423702900045
Klíčová slova anglicky
iron; phosphonate; hexanuclear; Moessbauer spectroscopy;antiferromagnetic coupling
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 23. 4. 2024 11:02, Mgr. Michal Petr
Anotace
V originále
A new hexanuclear molecular iron phosphonate complex, [Fe-6(HAIPA)(12)(OH)(6)]center dot nH(2)O (1 center dot n(2)O) (H(2)AIPA = NH2(CH3)(2)CP(O)(OH)(2), (2-aminopropan-2-yl) phosphonic acid), was synthesized from Fe2+ and Fe3+ salts in water by interaction with the ligand salts. Addition of corresponding amounts of sodium or tetramethylammonium salts of H2AIPA to the solution of iron precursors led to the formation of large bright-green crystals of complex 1. Isolated products were studied by spectroscopic and analytical methods -IR, Mossbauer spectroscopy, TG/DSC, ICP-OES, and CHN analysis. A novel {Fe-6} hexanuclear molecular structure of 1 was confirmed by single crystal X-ray diffraction analysis. An octahedral coordination environment of iron cations is formed by phosphonate and hydroxo oxygens. Twelve phosphonate groups and six -OH groups act as bridging ligands and bind six Fe octahedra. Because of protonation of the amino group, the phosphonate anions coordinate in the zwitterionic form as HAIPA(-) (NH3+(CH3)(2)CPO32-). The iron cations are present in the form of high-spin Fe3+, which was confirmed by the bond valence sum (BVS) calculations and the Fe-57 Mossbauer spectra. The magnetic measurements show antiferromagnetic coupling between the iron centers with decreasing temperature.
Návaznosti
LM2015043, projekt VaV |
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LQ1601, projekt VaV |
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