Cationic Organomagnesium Complexes as Highly Active Initiators for the Ring-Opening Polymerization of ε-Caprolactone

Species of the form [LH]+[BR4]− (R = pentafluorophenyl, phenyl, 1) were synthesized by reaction of Brönsted acids with a novel bis-phosphinimine ligand (L = 4,6-(MesNPPh2)2dibenzofuran). Corresponding cationic complexes [LMg n Bu]+[BR4]− (2) were produced by reaction of [Mg n Bu2] with [LH]+[BR4]−...

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Veröffentlicht in:Organometallics 2010-03, Vol.29 (5), p.1079-1084
Hauptverfasser: Ireland, Benjamin J, Wheaton, Craig A, Hayes, Paul G
Format: Artikel
Sprache:eng
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Zusammenfassung:Species of the form [LH]+[BR4]− (R = pentafluorophenyl, phenyl, 1) were synthesized by reaction of Brönsted acids with a novel bis-phosphinimine ligand (L = 4,6-(MesNPPh2)2dibenzofuran). Corresponding cationic complexes [LMg n Bu]+[BR4]− (2) were produced by reaction of [Mg n Bu2] with [LH]+[BR4]−. Organomagnesium species 2a and 2b exhibit extremely high activity as initiators for the polymerization of ε-caprolactone, yielding near-quantitative conversion of monomer to high molecular weight (>2.0 × 105 g/mol) polymer in 4 min at ambient temperature.
ISSN:0276-7333
1520-6041
DOI:10.1021/om900669y