Communication
Bis(imino)pyridine Ligand Deprotonation Promoted by a Transient Iron Amide
Corresponding author. E-mail: pc92@cornell.edu.
Abstract

Addition of 2 equiv of LiNMe2 to the bis(imino)pyridine ferrous dichloride, (iPrPDI)FeCl2 (iPrPDI = (2,6-iPr2−C6H3N
CMe)2C5H3N), resulted in deprotonation of the chelate methyl groups, yielding the bis(enamide)pyridine iron dimethylamine adduct, (iPrPDEA)Fe(NHMe2) (iPrPDEA = (2,6-iPr2−C6H3NC
CH2)2C5H3N). Performing a similar procedure with KN(SiMe3)2 in THF solution afforded the corresponding bis(THF) adduct, (iPrPDEA)Fe(THF)2. (iPrPDEA)Fe(NHMe2) has also been prepared by addition of the free amine to the iron dialkyl complex, (iPrPDI)Fe(CH2SiMe3)2, implicating formation of a transient iron amide that is sufficiently basic to deprotonate the bis(imino)pyridine methyl groups. Deprotonation of the amine ligand in (iPrPDEA)Fe(NHMe2) has been accomplished by addition of amide bases to afford the ferrous amide-ate complexes, [(iPrPDEA)Fe(μ-NMe2)M] (M = Li, K).
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History
- Published In Issue January 09, 2006
- Received October 24, 2005
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CMe)2C5H3N; X = Cl, Br) with sodium amalgam under 1 atm of dinitrogen afforded the square pyramidal, high spin iron(0) bis(dinitrogen) complex (iPrPDI)Fe(...
CMe2)2C6H3N), with 1 equiv of N2CHSiMe3 afforded the corresponding iron diazoalkane compound, (iPrPDI)Fe(N2CHSiMe3). Spectroscopic studies in ...

