a variety of group 4 metal catalytic systems (c2-symmetric {ebthi}-, {sbi}-type zirconocene complexes (c2-1–4); c1-symmetric (c1-5–8) and cs-symmetric (cs-9) {cp/flu}-type zirconocene complexes; cp*2zrcl2 (cp* 2-10)), half-metallocene complexes (cpticl3, hm-11), constrained-geometry (cgc-12) titanium catalysts) and post-metallocene catalysts (dow’s ortho-metallated amido-pyridino hafnium comple...

Group 4 metallocene complexes are effective catalysts in the ring-opening copolymerisation of epoxides and anhydrides to afford bio-derived polymers.

Reaction of the PEt3 adduct of a disilylated five-membered cyclic germylene with group 4 metallocene dichlorides in the presence of magnesium led to the formation of the respective germylene metallocene phosphine complexes of titanium, zirconium, and hafnium. Attempts to react the related NHC adduct of a disilylated four-membered cyclic germylene under the same conditions with Cp2TiCl2 did not ...

Metallocene and ansa-metallocene complexes of group 3 metals and the Lanthanides have shown to be effective catalysts for a number of chemical reactions. These include alkene polymerization, hydrosilation, hydroboration, hydrogenation and hydroamination. The coordinatively unsaturated, monomeric permethylyttrocene complexes in particular have proven to be highly effective for carrying out these...

Reduction of group 4 metallocene dichlorides with magnesium in the presence of cyclic disilylated stannylene or plumbylene phosphine adducts yielded the respective metallocene tetrylene phosphine complexes. Under the same conditions the use of the respective dimerized stannylene or plumbylene gave metallocene ditetrylene complexes. A computational analysis of these reactions revealed for all in...

A study of the full dehydrogenation of hydrazine borane (H2N-NH2·BH3) to give H2 and N2 as gaseous products catalysed by a variety of group 4 metallocene alkyne complexes of the type CpM(L)(η(2)-Me3SiC2SiMe3) (Cp' = substituted or unsubstituted η(5)-cyclopentadienyl; M = Ti, no L; M = Zr, L = pyridine) and group 4 metallocene hydrides is presented. Volumetric data show that the amount of hydrog...

A variety of group 4 metal catalytic systems (C2-symmetric {EBTHI}-, {SBI}-type zirconocene complexes (C2-1–4); C1-symmetric (C1-5–8) and Cs-symmetric (Cs-9) {Cp/Flu}-type zirconocene complexes; Cp*2ZrCl2 (Cp* 2-10)), half-metallocene complexes (CpTiCl3, HM-11), constrained-geometry (CGC-12) titanium catalysts) and post-metallocene catalysts (Dow’s ortho-metallated amido-pyridino hafnium comple...

New permethylindenyl-phenoxide (PHENI*) ansa -metallocene titanium complexes immobilised on inorganic solid supports are highly effective catalysts for ethylene polymerisation capable of producing disentangled ultra-high molecular weight polyethylene.

Functional group transformations at the group 4 metallocene framework have been demonstrated, which have provided relatively straightforward access to otherwise synthetically challenging derivatives. The pendant nitrile group in Ti and Zr metallocene complexes of the type [(η(5)-C5Me5)(η(5)-C5H4CMe2CH2CN)MCl2] was converted into an intramolecularly bound ketimido moiety by alkylation, which too...

Dehydrogenation of Me(2)NH·BH(3) (1) by group 4 metallocene alkyne complexes of the type Cp(2)M(L)(η(2)-Me(3)SiC(2)SiMe(3)) [Cp = η(5)-cyclopentadienyl; M = Ti, no L (2Ti); M = Zr, L = pyridine (2Zr)] and group 4 metal amido complexes of the type M(NMe(2))(4) [M = Ti (8Ti), Zr (8Zr)] is presented.