Accessibility and selective stabilization of the principal spin states of iron by pyridyl versus phenolic ketimines: Modulation of the 6 A 12 T 2 ground-state transformation of the [FeN4O2]+ chromophore

Musa S. Shongwe, Usama A. Al-Zaabi, Faizah Al-Mjeni, Carla S. Eribal, Ekkehard Sinn, Imaddin A. Al-Omari, Hussein H. Hamdeh, Dariusz Matoga, Harry Adams, Michael J. Morris, Arnold L. Rheingold, Eckhard Bill, David J. Sellmyer

Research output: Contribution to journalArticle

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Abstract

Several potentially tridentate pyridyl and phenolic Schiff bases (apRen and HhapRen, respectively) were derived from the condensation reactions of 2-acetylpyridine (ap) and 2′-hydroxyacetophenone (Hhap), respectively, with N-R-ethylenediamine (RNHCH2CH2NH2, Ren; R = H, Me or Et) and complexed in situ with iron(II) or iron(III), as dictated by the nature of the ligand donor set, to generate the six-coordinate iron compounds [FeII(apRen)2]X2 (R = H, Me; X - = ClO4-, BPh4-, PF 6-) and [FeIII(hapRen)2]X (R = Me, Et; X- = ClO4-, BPh4-). Single-crystal X-ray analyses of [FeII(apRen)2](ClO 4)2 (R = H, Me) revealed a pseudo-octahedral geometry about the ferrous ion with the FeII-N bond distances (1.896-2.041 Å) pointing to the 1A1 (dπ 6) ground state; the existence of this spin state was corroborated by magnetic susceptibility measurements and Mössbauer spectroscopy. In contrast, the X-ray structure of the phenolate complex [FeIII(hapMen) 2]ClO4, determined at 100 K, demonstrated stabilization of the ferric state; the compression of the coordinate bonds at the metal center is in accord with the 2T2 (dπ5) ground state. Magnetic susceptibility measurements along with EPR and Mössbauer spectroscopic techniques have shown that the iron(III) complexes are spin-crossover (SCO) materials. The spin transition within the [Fe IIIN4O2]+ chromophore was modulated with alkyl substituents to afford two-step and one-step 6A 12T2 transformations in [Fe III(hapMen)2]ClO4 and [FeIII(hapEen) 2]ClO4, respectively. Previously, none of the X-salRen- and X-sal2trien-based ferric spin-crossover compounds exhibited a stepwise transition. The optical spectra of the LS iron(II) and SCO iron(III) complexes display intense dπ → pπ* and pπ → dπ CT visible absorptions, respectively, which account for the spectacular color differences. All the complexes are redox-active; as expected, the one-electron oxidative process in the divalent compounds occurs at higher redox potentials than does the reverse process in the trivalent compounds. The cyclic voltammograms of the latter compounds reveal irreversible electrochemical generation of the phenoxyl radical. Finally, the H2salen-type quadridentate ketimine H2hapen complexed with an equivalent amount of iron(III) to afford the μ-oxo-monobridged dinuclear complex [{FeIII(hapen)}2(μ-O)] exhibiting a distorted square-pyramidal geometry at the metal centers and considerable antiferromagnetic coupling of spins (J ≈ -99 cm-1).

Original languageEnglish
Pages (from-to)8241-8253
Number of pages13
JournalInorganic Chemistry
Volume51
Issue number15
DOIs
Publication statusPublished - Aug 6 2012

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Chromophores
Ground state
chromophores
Iron
Stabilization
stabilization
Modulation
modulation
iron
ground state
crossovers
ethylenediamine
Magnetic susceptibility
Metals
Iron Compounds
iron compounds
magnetic permeability
ketimine
X rays
Condensation reactions

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Physical and Theoretical Chemistry

Cite this

Accessibility and selective stabilization of the principal spin states of iron by pyridyl versus phenolic ketimines : Modulation of the 6 A 12 T 2 ground-state transformation of the [FeN4O2]+ chromophore. / Shongwe, Musa S.; Al-Zaabi, Usama A.; Al-Mjeni, Faizah; Eribal, Carla S.; Sinn, Ekkehard; Al-Omari, Imaddin A.; Hamdeh, Hussein H.; Matoga, Dariusz; Adams, Harry; Morris, Michael J.; Rheingold, Arnold L.; Bill, Eckhard; Sellmyer, David J.

In: Inorganic Chemistry, Vol. 51, No. 15, 06.08.2012, p. 8241-8253.

Research output: Contribution to journalArticle

Shongwe, Musa S. ; Al-Zaabi, Usama A. ; Al-Mjeni, Faizah ; Eribal, Carla S. ; Sinn, Ekkehard ; Al-Omari, Imaddin A. ; Hamdeh, Hussein H. ; Matoga, Dariusz ; Adams, Harry ; Morris, Michael J. ; Rheingold, Arnold L. ; Bill, Eckhard ; Sellmyer, David J. / Accessibility and selective stabilization of the principal spin states of iron by pyridyl versus phenolic ketimines : Modulation of the 6 A 12 T 2 ground-state transformation of the [FeN4O2]+ chromophore. In: Inorganic Chemistry. 2012 ; Vol. 51, No. 15. pp. 8241-8253.
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title = "Accessibility and selective stabilization of the principal spin states of iron by pyridyl versus phenolic ketimines: Modulation of the 6 A 1 ↔ 2 T 2 ground-state transformation of the [FeN4O2]+ chromophore",
abstract = "Several potentially tridentate pyridyl and phenolic Schiff bases (apRen and HhapRen, respectively) were derived from the condensation reactions of 2-acetylpyridine (ap) and 2′-hydroxyacetophenone (Hhap), respectively, with N-R-ethylenediamine (RNHCH2CH2NH2, Ren; R = H, Me or Et) and complexed in situ with iron(II) or iron(III), as dictated by the nature of the ligand donor set, to generate the six-coordinate iron compounds [FeII(apRen)2]X2 (R = H, Me; X - = ClO4-, BPh4-, PF 6-) and [FeIII(hapRen)2]X (R = Me, Et; X- = ClO4-, BPh4-). Single-crystal X-ray analyses of [FeII(apRen)2](ClO 4)2 (R = H, Me) revealed a pseudo-octahedral geometry about the ferrous ion with the FeII-N bond distances (1.896-2.041 {\AA}) pointing to the 1A1 (dπ 6) ground state; the existence of this spin state was corroborated by magnetic susceptibility measurements and M{\"o}ssbauer spectroscopy. In contrast, the X-ray structure of the phenolate complex [FeIII(hapMen) 2]ClO4, determined at 100 K, demonstrated stabilization of the ferric state; the compression of the coordinate bonds at the metal center is in accord with the 2T2 (dπ5) ground state. Magnetic susceptibility measurements along with EPR and M{\"o}ssbauer spectroscopic techniques have shown that the iron(III) complexes are spin-crossover (SCO) materials. The spin transition within the [Fe IIIN4O2]+ chromophore was modulated with alkyl substituents to afford two-step and one-step 6A 1 ↔ 2T2 transformations in [Fe III(hapMen)2]ClO4 and [FeIII(hapEen) 2]ClO4, respectively. Previously, none of the X-salRen- and X-sal2trien-based ferric spin-crossover compounds exhibited a stepwise transition. The optical spectra of the LS iron(II) and SCO iron(III) complexes display intense dπ → pπ* and pπ → dπ CT visible absorptions, respectively, which account for the spectacular color differences. All the complexes are redox-active; as expected, the one-electron oxidative process in the divalent compounds occurs at higher redox potentials than does the reverse process in the trivalent compounds. The cyclic voltammograms of the latter compounds reveal irreversible electrochemical generation of the phenoxyl radical. Finally, the H2salen-type quadridentate ketimine H2hapen complexed with an equivalent amount of iron(III) to afford the μ-oxo-monobridged dinuclear complex [{FeIII(hapen)}2(μ-O)] exhibiting a distorted square-pyramidal geometry at the metal centers and considerable antiferromagnetic coupling of spins (J ≈ -99 cm-1).",
author = "Shongwe, {Musa S.} and Al-Zaabi, {Usama A.} and Faizah Al-Mjeni and Eribal, {Carla S.} and Ekkehard Sinn and Al-Omari, {Imaddin A.} and Hamdeh, {Hussein H.} and Dariusz Matoga and Harry Adams and Morris, {Michael J.} and Rheingold, {Arnold L.} and Eckhard Bill and Sellmyer, {David J.}",
year = "2012",
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TY - JOUR

T1 - Accessibility and selective stabilization of the principal spin states of iron by pyridyl versus phenolic ketimines

T2 - Modulation of the 6 A 1 ↔ 2 T 2 ground-state transformation of the [FeN4O2]+ chromophore

AU - Shongwe, Musa S.

AU - Al-Zaabi, Usama A.

AU - Al-Mjeni, Faizah

AU - Eribal, Carla S.

AU - Sinn, Ekkehard

AU - Al-Omari, Imaddin A.

AU - Hamdeh, Hussein H.

AU - Matoga, Dariusz

AU - Adams, Harry

AU - Morris, Michael J.

AU - Rheingold, Arnold L.

AU - Bill, Eckhard

AU - Sellmyer, David J.

PY - 2012/8/6

Y1 - 2012/8/6

N2 - Several potentially tridentate pyridyl and phenolic Schiff bases (apRen and HhapRen, respectively) were derived from the condensation reactions of 2-acetylpyridine (ap) and 2′-hydroxyacetophenone (Hhap), respectively, with N-R-ethylenediamine (RNHCH2CH2NH2, Ren; R = H, Me or Et) and complexed in situ with iron(II) or iron(III), as dictated by the nature of the ligand donor set, to generate the six-coordinate iron compounds [FeII(apRen)2]X2 (R = H, Me; X - = ClO4-, BPh4-, PF 6-) and [FeIII(hapRen)2]X (R = Me, Et; X- = ClO4-, BPh4-). Single-crystal X-ray analyses of [FeII(apRen)2](ClO 4)2 (R = H, Me) revealed a pseudo-octahedral geometry about the ferrous ion with the FeII-N bond distances (1.896-2.041 Å) pointing to the 1A1 (dπ 6) ground state; the existence of this spin state was corroborated by magnetic susceptibility measurements and Mössbauer spectroscopy. In contrast, the X-ray structure of the phenolate complex [FeIII(hapMen) 2]ClO4, determined at 100 K, demonstrated stabilization of the ferric state; the compression of the coordinate bonds at the metal center is in accord with the 2T2 (dπ5) ground state. Magnetic susceptibility measurements along with EPR and Mössbauer spectroscopic techniques have shown that the iron(III) complexes are spin-crossover (SCO) materials. The spin transition within the [Fe IIIN4O2]+ chromophore was modulated with alkyl substituents to afford two-step and one-step 6A 1 ↔ 2T2 transformations in [Fe III(hapMen)2]ClO4 and [FeIII(hapEen) 2]ClO4, respectively. Previously, none of the X-salRen- and X-sal2trien-based ferric spin-crossover compounds exhibited a stepwise transition. The optical spectra of the LS iron(II) and SCO iron(III) complexes display intense dπ → pπ* and pπ → dπ CT visible absorptions, respectively, which account for the spectacular color differences. All the complexes are redox-active; as expected, the one-electron oxidative process in the divalent compounds occurs at higher redox potentials than does the reverse process in the trivalent compounds. The cyclic voltammograms of the latter compounds reveal irreversible electrochemical generation of the phenoxyl radical. Finally, the H2salen-type quadridentate ketimine H2hapen complexed with an equivalent amount of iron(III) to afford the μ-oxo-monobridged dinuclear complex [{FeIII(hapen)}2(μ-O)] exhibiting a distorted square-pyramidal geometry at the metal centers and considerable antiferromagnetic coupling of spins (J ≈ -99 cm-1).

AB - Several potentially tridentate pyridyl and phenolic Schiff bases (apRen and HhapRen, respectively) were derived from the condensation reactions of 2-acetylpyridine (ap) and 2′-hydroxyacetophenone (Hhap), respectively, with N-R-ethylenediamine (RNHCH2CH2NH2, Ren; R = H, Me or Et) and complexed in situ with iron(II) or iron(III), as dictated by the nature of the ligand donor set, to generate the six-coordinate iron compounds [FeII(apRen)2]X2 (R = H, Me; X - = ClO4-, BPh4-, PF 6-) and [FeIII(hapRen)2]X (R = Me, Et; X- = ClO4-, BPh4-). Single-crystal X-ray analyses of [FeII(apRen)2](ClO 4)2 (R = H, Me) revealed a pseudo-octahedral geometry about the ferrous ion with the FeII-N bond distances (1.896-2.041 Å) pointing to the 1A1 (dπ 6) ground state; the existence of this spin state was corroborated by magnetic susceptibility measurements and Mössbauer spectroscopy. In contrast, the X-ray structure of the phenolate complex [FeIII(hapMen) 2]ClO4, determined at 100 K, demonstrated stabilization of the ferric state; the compression of the coordinate bonds at the metal center is in accord with the 2T2 (dπ5) ground state. Magnetic susceptibility measurements along with EPR and Mössbauer spectroscopic techniques have shown that the iron(III) complexes are spin-crossover (SCO) materials. The spin transition within the [Fe IIIN4O2]+ chromophore was modulated with alkyl substituents to afford two-step and one-step 6A 1 ↔ 2T2 transformations in [Fe III(hapMen)2]ClO4 and [FeIII(hapEen) 2]ClO4, respectively. Previously, none of the X-salRen- and X-sal2trien-based ferric spin-crossover compounds exhibited a stepwise transition. The optical spectra of the LS iron(II) and SCO iron(III) complexes display intense dπ → pπ* and pπ → dπ CT visible absorptions, respectively, which account for the spectacular color differences. All the complexes are redox-active; as expected, the one-electron oxidative process in the divalent compounds occurs at higher redox potentials than does the reverse process in the trivalent compounds. The cyclic voltammograms of the latter compounds reveal irreversible electrochemical generation of the phenoxyl radical. Finally, the H2salen-type quadridentate ketimine H2hapen complexed with an equivalent amount of iron(III) to afford the μ-oxo-monobridged dinuclear complex [{FeIII(hapen)}2(μ-O)] exhibiting a distorted square-pyramidal geometry at the metal centers and considerable antiferromagnetic coupling of spins (J ≈ -99 cm-1).

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