Jump to main content
Jump to site search

Issue 41, 2009
Previous Article Next Article

Synthesis, structure and ethylene polymerisation behaviour of vanadium(IV and V) complexes bearing chelating aryloxides

Author affiliations

Abstract

The reaction of [V(Np-tolyl)Cl3] with the sulfur-bridged diphenol ligand 2,2′-thiobis(4,6-di-tert-butylphenol), {2,2′-S[4,6-(t-Bu)2C6H2OH]2} (LSH2) afforded the complexes [V(LS)2] (1) and [VOCl3(MeCN)2][H3Np-tolyl] (2). Complex 2 could also be prepared directly from [V(Np-tolyl)Cl3] and ‘wet’ acetonitrile. Reaction of [V(Np-tolyl)(Ot-Bu)3] with LSH2 afforded [VO(μ2-OH)(LS)]2·6(MeCN) (3), whilst reaction of [VO(On-Pr)3] with 2,2′-sulfinylbis(4,6-di-tert-butylphenol), {2,2′-SO2[4,6-(t-Bu)2C6H2OH]2} (LSO2H2), afforded [V(LSO2)2]·MeCN (4). The reaction of [VO(Oi-Pr)3] with the ethylidene-bridged diphenol 2,2′-ethylidenebis(4,6-di-tert-butylphenol), {2,2′-CH3CH[4,6-(t-Bu)2C6H2OH]2} (LH2) afforded the hydroxyl bridged complexes [(VOL)22-OH)(μ2-Oi-Pr)] (5) (major product) and [VO(μ2-OH)(L)]2·4(MeCN) (6) (minor product). In general, we find that controlled hydrolysis of [V(NAr)(On-Pr)3] (Ar = p-ClC6H4, p-OCNC6H4 or p-tolyl) in the presence of LH2 reproducibly led to the vanadyl complex [VO(μ-On-Pr)L]2·2(MeCN) (7), in which the n-propoxide bridges both unexpectedly lie above the V2O2 plane. Reaction of the linear triphenol 2,6-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-4-tert-butylphenol, [ArCH2Ar1CH2Ar] (Ar = 4,6-di-tert-butylphenol; Ar1 = 4-tert-butylphenol) (L1H3), and [VO(On-Pr)3] afforded the complex [VOL1]2·3(MeCN) (8), whilst reaction of [V(Np-tolyl)(Oi-Pr)3] with the related methylene-bridged linear triphenol 2,6-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-4-methylphenol, [ArCH2Ar2CH2Ar] (L2H3) (Ar2 = 4-methylphenol), gave {[V(μ2-O)(Np-tolyl)][VO(Oi-Pr)]L2}2·1.5(MeCN) (9). The crystal structures of 1 to 9 are reported. Complexes 14 and 79 were screened as pro-catalysts for the polymerisation of ethylene in the presence of the co-catalyst dimethylaluminium chloride (DMAC) and the re-activator ethyltrichloroacetate (ETA). All are highly active ethylene polymerisation catalysts with activities covering the range 2000 to 90 000 g mmol−1 h−1bar−1, and these results are discussed in terms of the ligands present at vanadium in the pro-catalyst. Complex 3 has also been screened for ethylene/propylene copolymerisation.

Graphical abstract: Synthesis, structure and ethylene polymerisation behaviour of vanadium(iv and v) complexes bearing chelating aryloxides

Back to tab navigation

Supplementary files

Publication details

The article was received on 28 Jan 2009, accepted on 15 May 2009 and first published on 07 Jul 2009


Article type: Paper
DOI: 10.1039/B901810G
Citation: Dalton Trans., 2009,0, 8900-8910
  •   Request permissions

    Synthesis, structure and ethylene polymerisation behaviour of vanadium(IV and V) complexes bearing chelating aryloxides

    D. Homden, C. Redshaw, L. Warford, D. L. Hughes, J. A. Wright, S. H. Dale and M. R. J. Elsegood, Dalton Trans., 2009, 0, 8900
    DOI: 10.1039/B901810G

Search articles by author

Spotlight

Advertisements