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The well-known catalyst precursor 2,6-bis[1-((2,6-diisopropylphenyl)imino)ethyl]pyridine ( 1 ) is functionalized by various alkenyl groups to yield the corresponding alkenyl-functionalized 2,6-bis[1-((2,6-diisopropylphenyl)imino)ethyl]pyridine ligand. Reaction of these novel functionalized bis(imino)pyridyl ligands with iron(II) chloride results in the formation of precatalysts 5 − 7, which possess different spacer moieties. The possibility of self-immobilization has been investigated with respect to the chain length of the alkenyl moiety. Additionally, experiments to heterogenize these functionalized iron(II) complexes on modified silica via hydrosilation are presented ( 8 − 10 ). The immobilization has been studied by IR, and the resulting polymers have been characterized by GPC and static light scattering.
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Kaul et al. (2001) studied this question.
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