Half-sandwich Mo(III) complexes with asymmetric diazadiene ligands

François Stoffelbach (1) , Philippe Richard (1) , Rinaldo Poli (2) , Titus Jenny (3) , Corinne Savary (3)

1 LSEO - Laboratoire de Synthèse et Electrosynthèse Organométalliques
2 LCC - Laboratoire de chimie de coordination
3 UNIFR - Université de Fribourg = University of Fribourg

The asymmetric 1,4-diazadiene ligands R*N=CHCH=NR* [R* = (S)-CH(CH3)Ph], R*2dad, and 2,2’-bis(4-ethyloxazoline), as-ox, have been used to generate half-sandwich MoIII derivatives by addition to Cp2Mo2Cl4. Ligand R*2dad affords a mononuclear, paramagnetic 17-electron product, CpMoCl2(R*2dad), whereas as-ox leads to the isolation of a dinuclear compound where only one molecule of ligand has been added per two Mo atoms, Cp2Mo2Cl4(as-ox). In the presence of free as-ox, this compound coexists with the paramagnetic mononuclear complex in solution. Both products are capable to control the radical polymerization of styrene under typical atom transfer radical polymerization (ATRP) conditions. However, the tacticity of the resulting polystyrene does not differ from that given by conventional free radical polymerization.

Mots clés: Molybdenum; Atom transfer radical polymerization; Polystyrene; Half-sandwich complexes; Diazadiene

Domaines: Chimie de coordination; Catalyse; Polymères

François Stoffelbach, Philippe Richard, Rinaldo Poli, Titus Jenny, Corinne Savary. Half-sandwich Mo(III) complexes with asymmetric diazadiene ligands. Inorganica Chimica Acta, 2006, 359 (14), pp.4447-4453. ⟨10.1016/j.ica.2006.04.013⟩. ⟨hal-03195897⟩