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Highly Active Multidentate Ligand‐Based Alkyne Metathesis Catalysts
Authors:Dr Ya Du  Dr Haishen Yang  Chengpu Zhu  Michael Ortiz  Kenji D Okochi  Prof?Dr Richard Shoemaker  Dr Yinghua Jin  Prof?Dr Wei Zhang
Institution:Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO, USA
Abstract:Alkyne metathesis catalysts composed of molybdenum(VI) propylidyne and multidentate tris(2‐hydroxylbenzyl)methane ligands have been developed, which exhibit excellent stability (remains active in solution for months at room temperature), high activity, and broad functional‐group tolerance. The homodimerization and cyclooligomerization of monopropynyl or dipropynyl substrates, including challenging heterocycle substrates (e.g., pyridine), proceed efficiently at 40–55 °C in a closed system. The ligand structure and catalytic activity relationship has been investigated, which shows that the ortho groups of the multidentate phenol ligands are critical to the stability and activity of such a catalyst system.
Keywords:alkylidyne  alkyne metathesis  homogeneous catalysis  molybdenum  multidentate ligand
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