Synthesis of a Bis(thiophenolate)pyridine Ligand and Its Titanium, Zirconium, and Tantalum Complexes

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• 作者：Taylor N. Lenton ; David G. VanderVelde ; John E. Bercaw
• 刊名：Organometallics
• 出版年：2012
• 出版时间：November 12, 2012
• 年：2012
• 卷：31
• 期：21
• 页码：7492-7499
• 全文大小：440K
• 年卷期：v.31,no.21(November 12, 2012)
• ISSN：1520-6041

文摘

A precursor to a new tridentate LX₂ type ligand, bis(thiophenol)pyridine ((SNS)H₂ = (2-C₆H₄SH)₂-2,6-C₅H₃N), was prepared. Bis(thiophenolate)pyridine complexes of Ti, Zr, and Ta having dialkylamido coligands were synthesized and structurally characterized. The zirconium complex (SNS)Zr(NMe₂)₂ (4) displays C₂ symmetry in the solid state, unlike a related bis(phenolate)pyridine compound, C_s-symmetric (ONO)Ti(NMe₂)₂. This change is likely the result of strain about the sulfur atom in the six-membered chelate with longer metal鈥搒ulfur and carbon鈥搒ulfur bonds. Solid-state structures of tantalum complexes (SNS)Ta(NMe₂)₃ (5) and (SNS)TaCl(NEt₂)₂ (6) also display pronounced C₂ twisting of the SNS ligand. 1D and 2D NMR experiments show that 5 is fluxional, with rotation about the Ta鈥揘(amide) bonds occurring on the NMR time scale that interchange the equatorial amide methyl groups (螖G₃₉₃ = 25.0(3) kcal/mol). The fluxional behavior of 6 in solution was also studied by variable-temperature ¹H NMR. Observation of separate signals for the diastereotopic protons of the methylene unit of the diethylamide indicates that the complex remains locked on the NMR time scale in one diastereomeric conformation at temperatures below 鈭?0 掳C, fast rotation about the equatorial amide Ta鈥揘 bonds occurs at higher temperature (螖G₃₉₃ = 13.4(3) kcal/mol), and exchange of diastereomeric methylene protons occurs via inversion at Ta that interconverts antipodes (螖G₃₉₃ 鈮?14(1) kcal/mol).