Ethylene Polymerization at High Temperatures Catalyzed
by Double-Decker-Type Dinuclear Iron and Cobalt Complexes: Dimer Effect
on Stability of the Catalyst and Polydispersity of the Product
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Abstract
Dinuclear
Fe and Co complexes with a double-decker structure were
synthesized by using macrocyclic ligands having two bis(imino)pyridine
groups. X-ray crystallography of the dinuclear Co complex revealed
that the two bis(imino)pyridine Co moieties stack in an antiparallel
manner with a distance of 7.74 Å. A dinuclear Fe complex catalyzes
ethylene polymerization at 80–120 °C (5 atm ethylene)
to produce polymers with a relatively narrow molecular weight distribution
(<i>M</i><sub>w</sub>/<i>M</i><sub>n</sub> = 1.75–2.77);
its highest activity is 975 g (mmol Fe)<sup>−1</sup> h<sup>–1</sup> atm<sup>–1</sup> at 100 °C. Ethylene
polymerization at room temperature under 1 atm ethylene catalyzed
by the dinuclear Co and Fe complexes produces polymers with much higher
molecular weight (<i>M</i><sub>n</sub> up to 15.5-fold increase)
than the corresponding mononuclear complexes