Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Christoph Krüger
  • Peter Augustín
  • Ivan Nemec
  • Zdeňek Trávníček
  • Hiroki Oshio
  • Roman Boča
  • Franz Renz
  • Zdeňek Trávníček

Organisationseinheiten

Externe Organisationen

  • Slowakische Technische Universität Bratislava (STU)
  • Palacky University
  • University of Tsukuba
  • University of SS Cyril and Methodius, Trnava
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Details

OriginalspracheEnglisch
Seiten (von - bis)902-915
Seitenumfang14
FachzeitschriftEuropean Journal of Inorganic Chemistry
Ausgabenummer5-6
Frühes Online-Datum4 Dez. 2012
PublikationsstatusVeröffentlicht - Feb. 2013

Abstract

Iron(III) mononuclear complexes that involve pentadentate Schiff base ligands and chlorido, azido, cyanido, cyanato, thiocyanato, or selenocyanato coligands were synthesized, structurally characterized, and subjected to a magnetochemical investigation. The Schiff bases were derived either from 5-chlorosalicylaldehyde or the 2-hydroxyacetonaphthone analogues by using an asymmetric 1,6-diamino-4-azahexane. A polymorphism that originated from different pentadentate ligand conformations on the iron center or different arrangements of noncovalent contacts was detected for the thiocyan ato complexes. The central iron(III) atoms are mostly in the high-spin states, except for that with the coordinated cyanido ligand. Four complexes that contain the thiocyanato or selenocyanato ligand exhibit spin crossover, centered at the critical temperature (Tc) of 42, 114, 282, and 293 K, respectively. The magnetic data of all compounds were analyzed using the spin Hamiltonian formalism including the zerofield splitting (ZFS) term, and in the case of the spin-crossover compounds, the Ising-like model with vibrations was applied.

ASJC Scopus Sachgebiete

Zitieren

Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands. / Krüger, Christoph; Augustín, Peter; Nemec, Ivan et al.
in: European Journal of Inorganic Chemistry, Nr. 5-6, 02.2013, S. 902-915.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Krüger, C, Augustín, P, Nemec, I, Trávníček, Z, Oshio, H, Boča, R, Renz, F & Trávníček, Z 2013, 'Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands', European Journal of Inorganic Chemistry, Nr. 5-6, S. 902-915. https://doi.org/10.1002/ejic.201201038
Krüger, C., Augustín, P., Nemec, I., Trávníček, Z., Oshio, H., Boča, R., Renz, F., & Trávníček, Z. (2013). Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands. European Journal of Inorganic Chemistry, (5-6), 902-915. https://doi.org/10.1002/ejic.201201038
Krüger C, Augustín P, Nemec I, Trávníček Z, Oshio H, Boča R et al. Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands. European Journal of Inorganic Chemistry. 2013 Feb;(5-6):902-915. Epub 2012 Dez 4. doi: 10.1002/ejic.201201038
Krüger, Christoph ; Augustín, Peter ; Nemec, Ivan et al. / Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands. in: European Journal of Inorganic Chemistry. 2013 ; Nr. 5-6. S. 902-915.
Download
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T1 - Spin Crossover in Iron(III) Complexes with Pentadentate Schiff Base Ligands and Pseudohalido Coligands

AU - Krüger, Christoph

AU - Augustín, Peter

AU - Nemec, Ivan

AU - Trávníček, Zdeňek

AU - Oshio, Hiroki

AU - Boča, Roman

AU - Renz, Franz

AU - Trávníček, Zdeňek

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N2 - Iron(III) mononuclear complexes that involve pentadentate Schiff base ligands and chlorido, azido, cyanido, cyanato, thiocyanato, or selenocyanato coligands were synthesized, structurally characterized, and subjected to a magnetochemical investigation. The Schiff bases were derived either from 5-chlorosalicylaldehyde or the 2-hydroxyacetonaphthone analogues by using an asymmetric 1,6-diamino-4-azahexane. A polymorphism that originated from different pentadentate ligand conformations on the iron center or different arrangements of noncovalent contacts was detected for the thiocyan ato complexes. The central iron(III) atoms are mostly in the high-spin states, except for that with the coordinated cyanido ligand. Four complexes that contain the thiocyanato or selenocyanato ligand exhibit spin crossover, centered at the critical temperature (Tc) of 42, 114, 282, and 293 K, respectively. The magnetic data of all compounds were analyzed using the spin Hamiltonian formalism including the zerofield splitting (ZFS) term, and in the case of the spin-crossover compounds, the Ising-like model with vibrations was applied.

AB - Iron(III) mononuclear complexes that involve pentadentate Schiff base ligands and chlorido, azido, cyanido, cyanato, thiocyanato, or selenocyanato coligands were synthesized, structurally characterized, and subjected to a magnetochemical investigation. The Schiff bases were derived either from 5-chlorosalicylaldehyde or the 2-hydroxyacetonaphthone analogues by using an asymmetric 1,6-diamino-4-azahexane. A polymorphism that originated from different pentadentate ligand conformations on the iron center or different arrangements of noncovalent contacts was detected for the thiocyan ato complexes. The central iron(III) atoms are mostly in the high-spin states, except for that with the coordinated cyanido ligand. Four complexes that contain the thiocyanato or selenocyanato ligand exhibit spin crossover, centered at the critical temperature (Tc) of 42, 114, 282, and 293 K, respectively. The magnetic data of all compounds were analyzed using the spin Hamiltonian formalism including the zerofield splitting (ZFS) term, and in the case of the spin-crossover compounds, the Ising-like model with vibrations was applied.

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