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Chemistry

University of Nebraska - Lincoln

David Sellmyer Publications

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Full-Text Articles in Physics

Accessibility And Selective Stabilization Of The Principal Spin States Of Iron By Pyridyl Versus Phenolic Ketimines: Modulation Of The 6A1 ↔ 2T2 Ground-State Transformation Of The [Fen4O2]+ Chromophore, Musa S. Shongwe, Usama A. Al-Zaabi, Faizah Al-Mjeni, Carla S. Eribal, Imaddin A. Al-Omari, Hussein H. Hamdeh, Dariusz Matoga, Harry Adams, Michael J. Morris, Arnold L. Rheingold, Eckhard Bill, David J. Sellmyer Jan 2012

Accessibility And Selective Stabilization Of The Principal Spin States Of Iron By Pyridyl Versus Phenolic Ketimines: Modulation Of The 6A1 ↔ 2T2 Ground-State Transformation Of The [Fen4O2]+ Chromophore, Musa S. Shongwe, Usama A. Al-Zaabi, Faizah Al-Mjeni, Carla S. Eribal, Imaddin A. Al-Omari, Hussein H. Hamdeh, Dariusz Matoga, Harry Adams, Michael J. Morris, Arnold L. Rheingold, Eckhard Bill, David J. Sellmyer

David Sellmyer Publications

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 com-plexed 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–, PF6–) and [FeIII(hapRen)2]X (R = Me, Et; X– = ClO4–, BPh4–). Single-crystal X-ray …