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HERO ID
4281644
Reference Type
Journal Article
Title
Development of a new methodology for the synthesis of chloro(glycinato) 1, 10-phenanthroline copper(II) monohydrate and analogous complexes and study of their catalytic utility towards selective hydroxylation of phenol
Author(s)
Baruah, S; Puzari, A
Year
2017
Volume
47
Issue
11
Page Numbers
1542-1547
DOI
10.1080/24701556.2017.1357607
Web of Science Id
WOS:000422948400008
Abstract
A new simple and convenient method has been developed for the synthesis of copper(II) complexes using Proline and Glycine as ligand. The complexes were characterized by using conventional spectroscopic techniques and by determining structure. Methodology developed gives substantial yield of the products. Chloro(Glycinato) 1,10-Phenanthroline Copper(II) monohydrate and other complexes effectively catalyze the selective orthohydroxylation of phenol, in presence of Hydrogen peroxide, in water. Catechol formation was confirmed by IR and NMR spectroscopy. Hydroxylation reaction produces moderate to good yield of the product catechol. Longer time duration results in decrease of yield.
Keywords
1,10-Phenanthroline; Glycine; Methodology; Hydroxylation; Phenol; Catechol; Regioselectivity
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