Neutral and bis-cationic palladium(II) complexes with 1,2-bis(di(2-methoxyphenyl)phosphino)ethane (o-MeO-dppe) and 1,3-bis(di(2- methoxyphenyl)phosphino)propane (o-MeO-dppp) have been synthesized and employed to catalyze the CO-ethylene copolymerization reaction in either protic or aprotic solvents. A comparison of the catalytic performance of these complexes with that of analogous precursors stabilized by 1,2-bis(diphenylphosphino)ethane (dppe) and 1,3-bis(diphenylphosphino)propane (dppp) ligands has shown significant differences in terms of catalytic productivity and molecular weight. In situ and operando high-pressure NMR experiments have provided valuable information on catalysis resting states and intermediates and have contributed to rationalize the observed productivity as well.

CO-ethylene copolymerization reactions in different reaction media catalyzed by palladium(II) complexes with chelating diphosphines bearing ortho-methoxy-substituted aryl groups

Bianchini Claudio;Meli Andrea;Oberhauser Werner;
2007

Abstract

Neutral and bis-cationic palladium(II) complexes with 1,2-bis(di(2-methoxyphenyl)phosphino)ethane (o-MeO-dppe) and 1,3-bis(di(2- methoxyphenyl)phosphino)propane (o-MeO-dppp) have been synthesized and employed to catalyze the CO-ethylene copolymerization reaction in either protic or aprotic solvents. A comparison of the catalytic performance of these complexes with that of analogous precursors stabilized by 1,2-bis(diphenylphosphino)ethane (dppe) and 1,3-bis(diphenylphosphino)propane (dppp) ligands has shown significant differences in terms of catalytic productivity and molecular weight. In situ and operando high-pressure NMR experiments have provided valuable information on catalysis resting states and intermediates and have contributed to rationalize the observed productivity as well.
2007
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Copolymerization
Palladium
2
2
2-Trifluoroethanol
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/171025
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