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Iron complexes derived from {nacnac-(CH2py)2}- and {nacnac-(CH2py)(CHpy)}n ligands: stabilization of iron(II) via
Valerie A Williams1, Peter T Wolczanski, Jörg Sutter
1Baker Laboratory, Department of Chemistry & Chemical Biology, Cornell University , Ithaca, New York 14853, United States.
Abstract:
Nacnac-based tetradentate chelates, {nacnac-(CH2py)2}(-) ({nn(PM)2}(-)) and {nacnac-(CH2py)(CHpy)}(n) ({nn(PM)(PI)}(n)) have been investigated in iron complexes. Treatment of Fe{N(TMS)2}2(THF) with {nn(PM)2}H afforded {nn(PM)2}FeN(TMS)2 [1-N(TMS)2], which led to {nn(PM)2}FeCl (1-Cl) from HCl and to {nn(PM)2}FeN3 (1-N3) upon salt metathesis. Dehydroamination of 1-N(TMS)2 was induced by L (L = PMe3, CO) to afford {nn(PM)(PI)}Fe(PMe3)2 [2-(PMe3)2] and {nn(PM)(PI)}FeCO (3-CO). Substitution of 2-(PMe3)2 led to {nn(PM)(PI)}Fe(PMe3)CO [2-(PMe3)CO], and exposure to a vacuum provided {nn(PM)(PI)}Fe(PMe3) (3-PMe3). Metathesis routes to {nn(PM)(PI)}FeL2 (2-L2; L = PMe3, PMe2Ph) and {nn(PM)(PI)}FeL (3-L; L = PMePh2, PPh3) from [{nn(PM)(PI)}(2-)]Li2 and FeBr2(THF)2 in the presence of L proved feasible, and 1e(-) and 2e(-) oxidation of 2-(PMe3)2 afforded 2(+)-(PMe3)2 and 2(2+)-(PMe3)2 salts. Mössbauer spectroscopy, structural studies, and calculational assessments revealed the dominance of iron(II) in both high-spin (1-X) and low-spin (2-L2 and 3-L) environments, and the redox noninnocence (RNI) of {nn(PM)(PI)}(n) [2-L2, 3-L, n = 2-; 2(+)-(PMe3)2, n = 1-; 2(2+)-(PMe3)2, n = 0]. A discussion regarding the utility of RNI in chemical reactivity is proffered.
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