Related Experiment Video
Updated: Feb 20, 2026

A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
Published on: November 12, 2016
Lanthanoid Pseudo-Grignard Reagents: A Major Untapped Resource
Safaa H Ali1, Glen B Deacon2, Peter C Junk1
1College of Science & Engineering, James Cook University, Townsville, Qld., 4811, Australia.
Abstract:
Pseudo-Grignard reagents PhLnI (Ln=Yb, Eu), readily prepared by the oxidative addition of iodobenzene to ytterbium or europium metal at -78 °C in tetrahydrofuran (THF) or 1,2-dimethoxyethane (DME), react with a range of bulky N,N'-bis(aryl)formamidines to generate an extensive series of LnII or more rarely LnIII complexes, namely [Eu(DippForm)I(thf)4 ]⋅thf (1), [{EuI2 (dme)2 }2 ] (2), [Eu(XylForm)I(dme)2 ]⋅0.5 dme (3 a), [Eu(XylForm)I(dme)(μ-dme)]n (3 b), [{Eu(XylForm)I(μ-OH)(thf)2 }2 ] (4), [Yb(DippForm)I(thf)3 ]⋅thf (5 a), [Yb(DippForm)I2 (thf)3 ]⋅2 thf (5 b), [{Yb(MesForm)I(thf)2 }2 ] (6), [{Yb(XylForm)I(thf)2 }2 ] (7 a), and [Yb(XylForm)2 I(dme)]⋅dme (7 b) {(Form=ArNCHNAr; XylForm (Ar=2,6-Me2 C6 H3 ), MesForm (Ar=2,4,6-Me3 C6 H2 ), DippForm (Ar=2,6-iPr2 C6 H3 )}. Reaction of PhEuI and MesFormH in DME consistently gave 2, and reaction with XylFormH in THF gave 4. Europium complexes 1 and 3 a are seven-coordinate divalent monomers, whilst 3 b is a seven-coordinate dme-bridged polymer. Complex 5 a of the smaller YbII is a six-coordinate monomer, but the related 6 and 7 a are six-coordinate iodide-bridged dimers. 4 is a trivalent seven-coordinate hydroxide-bridged dimer, whereas complexes 5 b and 7 b are seven-coordinate monomeric YbIII derivatives. A characteristic structural feature is that iodide ligands are cisoid to the formamidinate ligand. To illustrate the synthetic scope of the pseudo-Grignard reagents, [Yb(Ph2 pz)I(thf)4 ] (Ph2 pz=3,5-diphenylpyrazolate) was oxidised with 1,2-diiodoethane to afford seven-coordinate monomeric pyrazolato-ytterbium(III) iodide [Yb(Ph2 Pz)I2 (thf)3 ] (8) in high yield, whilst metathesis between [Yb(Ph2 pz)I(thf)4 ] and NaCp (Cp=C5 H5 ) gave [Yb(C5 H5 )(Ph2 pz)(thf)]n (9), a nine-coordinate η5 :η5 -Cp-bridged coordination polymer. Reaction of the pseudo-Grignard reagent MeYbI with KN(SiMe3 )2 gave [K(dme)4 ][Yb{N(SiMe3 )2 }3 ] (10) with a charge-separated three-coordinate homoleptic [Yb{N(SiMe3 )2 }3 ]- anion, a complex that could be obtained in high yield by deliberate synthesis from YbI2 and KN(SiMe3 )2 in DME.
More Related Videos
10:10Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
Published on: July 28, 2018
09:58Metal-free Synthesis of Ynones from Acyl Chlorides and Potassium Alkynyltrifluoroborate Salts
Published on: February 24, 2015
Related Concept Videos
Acid Halides to Alcohols: Grignard Reaction
Grignard reagents are a source of carbanions and function as nucleophiles. The mechanism begins with the nucleophilic attack by the carbanion at the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs,...
Nitriles to Ketones: Grignard Reaction
The mechanism begins with a nucleophilic attack by the Grignard...
Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents
Esters to Alcohols: Grignard Reaction
The reaction requires two equivalents of the Grignard reagent and introduces two identical alkyl groups, derived from the Grignard reagent, bonded to the hydroxyl-bearing carbon of the alcohol.
The reaction follows the typical nucleophilic acyl substitution mechanism. The Grignard...
Alcohols from Carbonyl Compounds: Grignard Reaction
Magnesium from the reagent coordinates with carbonyl oxygen, further reducing the carbonyl carbon's electron density. Thus, the...
Acid Halides to Ketones: Gilman Reagent
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...