Journal
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 696, Issue 6, Pages 1258-1261Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2010.11.035
Keywords
Zirconium; Sulfur; Cyclooctane; [OSSO]-type ligand; Dialkyl complexes
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Funding
- JSPS
- Mitsubishi Chemical Corporation
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Dimethyl and bis[(trimethylsilyl) methyl] zirconium complexes ([OSSO]ZrR2) [4, R = Me; 5, R = CH2SiMe3] having [OSSO]-type bis(phenolato) ligand 1 based on the trans-1,2-cyclooctanediylbis(thio) core have been synthesized by the reactions of the corresponding dichloro zirconium complex 3 with 2 equiv. of MeMgBr and Me3SiCH2MgCl, respectively, in Et2O/toluene at -78 degrees C. The molecular structures of these complexes 3-5 were characterized by NMR spectroscopy, elemental analyses, and X-ray crystallography. H-1 and C-13 NMRdata of complexes 3-5 exhibited that they took the C-2-symmetry in solution in the NMRtime scale. In the crystal structures of 3-5, each zirconium center lies at the center of a distorted octahedral coordination sphere with cis sulfur atoms and trans oxygen atoms, which adopts a cis-alpha [(Lambda*, S*, S*)] configuration. (C) 2010 Elsevier B.V. All rights reserved.
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