Abstract

Abstract The oxo-bridged dinuclear complex [Mo2O4(μ2-O)Cl2(pypzEA)2] (2) (pypzEA = ethyl[3-(pyridin-2-yl)-1H-pyrazol-1-yl]acetate) was obtained upon the treatment of [MoO2Cl2(pypzEA)] (1) with ethanol. The molecular structure of 2 consists of two highly distorted {MoClN2O3} octahedra sharing a corner oxygen atom, with a Mo O Mo “kink” angle of 163.2(2)° and a Mo⋯Mo separation of 3.7029(7) A. Catalytic results with 2 for the epoxidation of cis-cyclooctene using tert-butylhydroperoxide as oxidant compare favorably with those reported for related oxomolybdenum(VI) complexes. The reaction is homogeneous in nature, and a fraction of 2 dissolves and is converted to other types of soluble active species, one of which was isolated and identified as the oxodiperoxo complex [MoO(O2)2(pypzEA)] (3).

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