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Epoxidation of alkenes using cost-effective green oxidant under eco-friend reaction condition

Authors: Agarwalla, Uday Sankar;

Epoxidation of alkenes using cost-effective green oxidant under eco-friend reaction condition

Abstract

Department of Chemistry, P. D. Women’s College, Jalpaiguri-735 101, West Bengal, India E-mail: udaygrwlla@gmail.com Manuscript received online 04 December 2019, revised 06 December 2019, accepted 09 December 2019 The catalytic properties of the mononuclear non-heme iron(III) complexes with N4 -donor ligands containing N,N´-bis(2- pyridylmethyl)-diamine moiety (diamines used are, 1,2-cyclohexanediamine in complex 1 and ethane-1,2-diamine in complex 2) have been investigated in the epoxidation of alkenes using green and environmentally benign hydrogen peroxide (H2O2 ) and tert-butyl hydroperoxide (tBuOOH) as terminal oxidants at room temperature. The analysis of the results obtained in the oxidation of cyclohexene suggests the involvement of radical-based pathway in the catalytic epoxidation reaction. The cataytic efficiency in terms of the yield of the oxidation products is found to be strongly dependent on the nature of the diamine moiety in the catalyst and the oxidant.

Keywords

catalysis, alkenes, epoxidation, tert-butyl hydroperoxide, hydrogen peroxide, Iron complexes

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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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