http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16859
Synthesis of palladium(II) complexes containing a new ±-D-xylofuranose-modified diphosphine and their application as catalyst precursors in the co- and terpolymerization of CO-ethene and propene (Articolo in rivista)
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- Label
- Synthesis of palladium(II) complexes containing a new ±-D-xylofuranose-modified diphosphine and their application as catalyst precursors in the co- and terpolymerization of CO-ethene and propene (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/b719748a (literal)
- Alternative label
Muñoz-Moreno, Bianca K.; Claver, Carmen; Ruiz, Aurora; Bianchini, Claudio; Meli, Andrea; Oberhauser, Werner (2008)
Synthesis of palladium(II) complexes containing a new ±-D-xylofuranose-modified diphosphine and their application as catalyst precursors in the co- and terpolymerization of CO-ethene and propene
in Dalton transactions (2003. Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Muñoz-Moreno, Bianca K.; Claver, Carmen; Ruiz, Aurora; Bianchini, Claudio; Meli, Andrea; Oberhauser, Werner (literal)
- Pagina inizio
- Pagina fine
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- ICCOM-CNR
Dept. de Quimica Fisica i Inorganica, Facultat de Quimica, Universitat Rovira i Virgili, c/Marcel.li Domingo, Tarragona, Spain (literal)
- Titolo
- Synthesis of palladium(II) complexes containing a new ±-D-xylofuranose-modified diphosphine and their application as catalyst precursors in the co- and terpolymerization of CO-ethene and propene (literal)
- Abstract
- The diphosphine 3,5-dideoxy-1,2-O-isopropylidene-3,5-bis(di(2-methoxyphenyl)phosphanyl)-a-Dxylofuranose
(o-MeO-xylophos), which differs from the known 3,5-dideoxy-1,2-O-isopropylidene-3,5-
bis(diphenylphosphanyl)-a-D-xylofuranose (xylophos) by the presence of 2-methoxy substituents on the
P-aryl rings, has been synthesized and characterized. These two ligands have been employed to stabilize
the PdII complexes [PdCl2(o-MeO-xylophos)] (1a), [PdCl2(xylophos)] (2a), [PdClMe(o-MeO-xylophos)]
(1b), [PdClMe(xylophos)] (2b), [Pd(OTs)(H2O)(o-MeO-xylophos)](OTs) (1c) and
[Pd(OTs)(H2O)(xylophos)](OTs) (2c). All complexes have been characterized by multinuclear-NMR
spectroscopy. The solid-state structure of 1a has been determined by a single crystal X-ray analysis. The
Pd-aqua complexes 1c and 2c have been employed to catalyse the CO-ethene and CO-propene
copolymerization as well as the CO-ethene-propene terpolymerization reaction in MeOH. The
catalytic activity and the molecular weight of the polyketones have been compared to those of the
products obtained with analogous catalysts, [Pd(H2O)2(o-MeO-dppp)](OTs)2 (3c) and
[Pd(H2O)(OTs)(dppp)](OTs) (4c), bearing the classical 1,3-bis(diphenylphoshino)propane ligand
(dppp). Under comparable catalytic conditions, all catalysts produce structurally similar polymeric
materials, with 1c yielding the largest propene incorporation as well as the highest productivity of
low-molecular-weight terpolymers. (literal)
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