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Current Organocatalysis

Editor-in-Chief

ISSN (Print): 2213-3372
ISSN (Online): 2213-3380

Macrocylic Picolinamide Complexes and their Catalytic Reactivity in Allylic Oxidation

Author(s): Peng Yu, Shu Gao and Ruiren Tang

Volume 2, Issue 2, 2015

Page: [203 - 211] Pages: 9

DOI: 10.2174/2213337202666150415004223

Price: $65

Abstract

This paper describes the synthesis, characterization and catalytic activities of three closed-loop picolinamide complexes. They were prepared by Mn(II), Cu(II), Co(II) acetate and macrocylic ligand (L), which was formed by the condensation between 2,6-pyridinedicarboxylic acid chloride and 2,6-diaminopyridine. These complexes have been characterized by XRD, 1H NMR, IR, UV-vis DRS, Element analysis and TGA. Their catalytic activities in allylic oxidation of cyclohexene and isophorone with molecular oxygen as primary terminal oxidant were investigated for the first time. The influences of reaction temperature, the amount of catalyst and reaction time on the oxidation of cyclohexene by Co-L were also investigated. The results show that the Co-L can be obtained optimum catalytic efficiency, giving 58.2% conversion of cyclohexene and maximum selectivity of 83.4% for 2-cyclohexene-1-one; 15.4% conversion of isophorone and 46.2% selectivity of ketoisophorone. The heterogeneous catalysts can be easily separated for reuse at least three times without any significant change in selectivity.

Keywords: Allylic oxidation, cyclohexene, macrocylic picolinamide, metal organic complexes, molecular oxygen, α-isophorone.

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