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Reaction environment and ligand lability in group 4 CpMXY (X, Y = Cl, OtBu) complexes.

作者信息

Boyde Nicholas C, Rightmire Nicholas R, Bierschenk Eric J, Steelman Grant W, Hanusa Timothy P, Brennessel William W

机构信息

Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.

Department of Chemistry, University of Rochester, Rochester, New York 14627, USA.

出版信息

Dalton Trans. 2016 Nov 22;45(46):18635-18642. doi: 10.1039/c6dt03199d.

Abstract

Despite their usefulness in catalytic and materials chemistry, the mixed cyclopentadienyl/alkoxide complexes of Ti, Zr, and Hf (CpM(OR)) have few reliable synthetic routes available to them. We describe the use of mechanical ball milling to promote halide metathesis from CpMCl, and compare these results to those obtained in hexanes and THF. Even without solvent, ring lability is extensive with titanium complexes, and alkoxide compounds with 0-3 Cp rings are isolated. The ball milling reactions are much faster than those in solution, but the distributions of products are similar to those obtained in hexanes, although different from those in THF. The range of compounds obtained from Zr and Hf starting materials is more limited, as Cp ring exchange does not occur.

摘要

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