The catalyst is named after German chemist Walter Kaminsky, who first described it in 1980 along with Hansjörg Sinn and others.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> Prior to Kaminsky's work, titanium chlorides supported on various materials were widely used (and still are) as heterogeneous catalysts for alkene polymerization. These halides are typically activated by treatment with trimethylaluminium. Kaminsky discovered that titanocene and related complexes emulated some aspects of these Ziegler–Natta catalysts but with low activity. He subsequently found that high activity could be achieved upon activation of these metallocenes with methylaluminoxane (MAO). The MAO serves two roles: (i) alkylation of the metallocene halide and (ii) abstraction of an anionic ligand (chloride or methyl) to give an electrophilic catalyst with a labile coordination site.<ref name=Kaminsky/><ref name=chen>Template:Cite journal</ref>
Ligand design
Kaminsky's discovery of well-defined, high activity homogeneous catalysts led to many innovations in the design of novel cyclopentadienyl ligands. These innovations include ansa-metallocenes, Cs-symmetric fluorenyl-Cp ligands,<ref>Template:Cite journal</ref> constrained geometry catalysts,<ref>Template:Cite journal</ref> Some Kaminsky-inspired catalysts use of chiral metallocenes that have bridged cyclopentadienyl rings. These innovations made possible highly stereoselective (or stereoregular) polymerization of α-olefins, some of which have been commercialized.<ref name=Klosin/>