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Abstract

Three new molybdenum (VI) complexes of 4,6-O-ethylidene-β-d-glucopyranosylamine derived ligands has been synthesized and the same has been used in the oxidation of thioanisole along with an earlier reported analogous complex. A selective oxidation of thioanisole to methyl phenyl sulphoxide in high yield is achieved using 1:1 mixture of thioanisole and urea hydrogen peroxide (UHP) in ethanol. A longer reaction time or excess of UHP, leads to the formation of corresponding sulphone, which was confirmed using HPLC and NMR measurements.

Graphical Abstract

The oxidation of thioanisole into corresponding sulphoxide and sulphone has been explored using dioxo-molybdenum (VI) complexes of 4,6-O-ethylidene-β-d-glucopyranosylamine derived Schiff base ligands.

Details

Title
Synthesis and Characterization of Glucose Derived Dioxo-molybdenum (VI) Complexes and Their Application in Sulphide Oxidation
Author
Sah, Ajay K 1 ; Baig, Noorullah 1 

 Department of Chemistry, Birla Institute of Technology and Science, Pilani, Pilani Campus, Rajasthan, India 
Pages
905-909
Publication year
2015
Publication date
Mar 2015
Publisher
Springer Nature B.V.
ISSN
1011372X
e-ISSN
1572879X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2258880504
Copyright
Catalysis Letters is a copyright of Springer, (2015). All Rights Reserved.