The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

  • M. Glöckle
  • W. Kaim
  • A. Klein
  • E. Roduner
  • G. Hübner
  • S. Zalis
  • J. Van Slageren
  • F. Renz
  • P. Gütlich

Organisationseinheiten

Externe Organisationen

  • Universität Stuttgart
  • Akademie Věd České Republiky (AV ČR)
  • Universiteit van Amsterdam (UvA)
  • Johannes Gutenberg-Universität Mainz
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Details

OriginalspracheEnglisch
Seiten (von - bis)2256-2262
Seitenumfang7
FachzeitschriftInorganic chemistry
Jahrgang40
Ausgabenummer10
PublikationsstatusVeröffentlicht - 7 Mai 2001

Abstract

The conceptually simple mixed-valent diiron compound (NEt4)5Fe(μ-tz)Fe(CN)5] with the 1,2,4,5-tetrazine (tz) bridging ligand was obtained as a thermally and air-stable material that displays large and highly variable electrochemical comproportionation constants between about 108 (in water) and 1019.0 (in acetonitrile). Strong metal-metal interaction is also evident from spectroscopic results obtained for the solid and for the dissolved species. The rather intense intervalence charge-transfer band occurs around 2400 nm; infrared and Mössbauer spectra reveal the high spectroscopic symmetry of the system according to an (Fe2.5)2 formulation. DFT calculations on the [(NC)5Fe(μ-tz)Fe(CN)5]6- ion confirm the presence of very low-lying π*(tz) and high-lying d(Fe) orbitals.

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The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states. / Glöckle, M.; Kaim, W.; Klein, A. et al.
in: Inorganic chemistry, Jahrgang 40, Nr. 10, 07.05.2001, S. 2256-2262.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Glöckle, M, Kaim, W, Klein, A, Roduner, E, Hübner, G, Zalis, S, Van Slageren, J, Renz, F & Gütlich, P 2001, 'The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states', Inorganic chemistry, Jg. 40, Nr. 10, S. 2256-2262. https://doi.org/10.1021/ic001229i
Glöckle, M., Kaim, W., Klein, A., Roduner, E., Hübner, G., Zalis, S., Van Slageren, J., Renz, F., & Gütlich, P. (2001). The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states. Inorganic chemistry, 40(10), 2256-2262. https://doi.org/10.1021/ic001229i
Glöckle M, Kaim W, Klein A, Roduner E, Hübner G, Zalis S et al. The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states. Inorganic chemistry. 2001 Mai 7;40(10):2256-2262. doi: 10.1021/ic001229i
Glöckle, M. ; Kaim, W. ; Klein, A. et al. / The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states. in: Inorganic chemistry. 2001 ; Jahrgang 40, Nr. 10. S. 2256-2262.
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title = "The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states",
abstract = "The conceptually simple mixed-valent diiron compound (NEt4)5Fe(μ-tz)Fe(CN)5] with the 1,2,4,5-tetrazine (tz) bridging ligand was obtained as a thermally and air-stable material that displays large and highly variable electrochemical comproportionation constants between about 108 (in water) and 1019.0 (in acetonitrile). Strong metal-metal interaction is also evident from spectroscopic results obtained for the solid and for the dissolved species. The rather intense intervalence charge-transfer band occurs around 2400 nm; infrared and M{\"o}ssbauer spectra reveal the high spectroscopic symmetry of the system according to an (Fe2.5)2 formulation. DFT calculations on the [(NC)5Fe(μ-tz)Fe(CN)5]6- ion confirm the presence of very low-lying π*(tz) and high-lying d(Fe) orbitals.",
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TY - JOUR

T1 - The stable diiron(2.5) complex ion [(NC)5Fe(μ-tz)Fe(CN)5]5-, tz = 1,2,4,5-tetrazine, and its neighboring oxidation states

AU - Glöckle, M.

AU - Kaim, W.

AU - Klein, A.

AU - Roduner, E.

AU - Hübner, G.

AU - Zalis, S.

AU - Van Slageren, J.

AU - Renz, F.

AU - Gütlich, P.

PY - 2001/5/7

Y1 - 2001/5/7

N2 - The conceptually simple mixed-valent diiron compound (NEt4)5Fe(μ-tz)Fe(CN)5] with the 1,2,4,5-tetrazine (tz) bridging ligand was obtained as a thermally and air-stable material that displays large and highly variable electrochemical comproportionation constants between about 108 (in water) and 1019.0 (in acetonitrile). Strong metal-metal interaction is also evident from spectroscopic results obtained for the solid and for the dissolved species. The rather intense intervalence charge-transfer band occurs around 2400 nm; infrared and Mössbauer spectra reveal the high spectroscopic symmetry of the system according to an (Fe2.5)2 formulation. DFT calculations on the [(NC)5Fe(μ-tz)Fe(CN)5]6- ion confirm the presence of very low-lying π*(tz) and high-lying d(Fe) orbitals.

AB - The conceptually simple mixed-valent diiron compound (NEt4)5Fe(μ-tz)Fe(CN)5] with the 1,2,4,5-tetrazine (tz) bridging ligand was obtained as a thermally and air-stable material that displays large and highly variable electrochemical comproportionation constants between about 108 (in water) and 1019.0 (in acetonitrile). Strong metal-metal interaction is also evident from spectroscopic results obtained for the solid and for the dissolved species. The rather intense intervalence charge-transfer band occurs around 2400 nm; infrared and Mössbauer spectra reveal the high spectroscopic symmetry of the system according to an (Fe2.5)2 formulation. DFT calculations on the [(NC)5Fe(μ-tz)Fe(CN)5]6- ion confirm the presence of very low-lying π*(tz) and high-lying d(Fe) orbitals.

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