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

Homden, Damien; Redshaw, Carl; Warford, Lee; Hughes, David L.; Wright, Joseph A.; Dale, Sophie H.; Elsegood, Mark R.J.

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 [VOCl 3(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)2C6H 2OH]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′-CH 3CH[4,6-(t-Bu)2C6H2OH]2} (LH2) afforded the hydroxyl bridged complexes [(VOL) 2(μ2-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, [ArCH2Ar1CH 2Ar] (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 1-4 and 7-9 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 90000 g mmol-1 h-1 bar-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. © 2009 The Royal Society of Chemistry.

Citation

Homden, D., Redshaw, C., Warford, L., Hughes, D. L., Wright, J. A., Dale, S. H., & Elsegood, M. R. (2009). Synthesis, structure and ethylene polymerisation behaviour of vanadium(iv and v) complexes bearing chelating aryloxides. Dalton Transactions : an international journal of inorganic chemistry, 8900-8910. https://doi.org/10.1039/b901810g

• Journal Article Type: Article
• Publication Date: Oct 21, 2009
• Deposit Date: Jun 8, 2022
• Journal: Dalton Transactions
• Print ISSN: 1477-9226
• Electronic ISSN: 1477-9234
• Publisher: Royal Society of Chemistry
• Peer Reviewed: Peer Reviewed
• Issue: 41
• Pages: 8900-8910
• DOI: https://doi.org/10.1039/b901810g
• Public URL: https://hull-repository.worktribe.com/output/3622516