Cationic zirconium complexes in situ generated from zirconium dibenzyl complexes bearing amine-bridged bis(phenolato) ligands have been developed to catalyze addition of C(sp(2))-H and C(sp(3))-H bonds of pyridine derivatives to alkenes. A series of zirconium complexes bearing different ligands have been synthesized, and their activities in catalyzing addition of C(sp(3))-H bonds of pyridine derivatives to alkenes have been studied and compared. Both reaction activity and regioselectivity are influenced by electronic and steric properties of ligand backbones. In addition, a cationic zirconium complex has been isolated and structurally characterized to shed some light on reaction mechanism.