A series of cyclic silylene-bridged (amidocyclopentadienyl)-dichlorotitanium(IV) complexes [TiCl 2 {η 5 -1-(CySitBuN-κN)-2,3,4,5-R 4 -C 5 }] was prepared, where CySi = silacyclobutyl (a), silacyclopentenyl (b), silacyclopentyl (c), and silacyclohexyl (d); R = H (4), Me (5). The starting silane, dichlorosilacycloalkane CySiCl 2 (1), was treated with NaCp (LiCp*), followed by LiNHtBu to yield the cyclic silylene-bridged ligands (R 4 C 5 )CySi(NHtBu) [R = H (2); Me (3)]. Subsequent deprotonation with n-butyllithium, followed by transmetalation with TiCl 4 yielded the desired constrained geometry complexes (CGCs) (CpCySiNtBu)TiCl 2 (4) and (Cp*CySiNtBu)TiCl 2 (5). The structures of the resulting cyclopentadienyl-(4b and 4c) and tetramethylcyclopentadienyl(silacycloalkyl)amidotitanium(IV) dichloride (5a, 5c, and 5d) species were studied by using X-ray crystallography to obtain geometrical information on cyclic silylene-modified CGCs. The ethylene polymerization by the cyclic silylene-bridged