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Biocidal and catalytic efficiency of ruthenium(III) complexes with tridentate Schiff base ligands
Author(s) -
Arunachalam S.,
Padma Priya N.,
Boopathi K.,
Jayabalakrishnan C.,
Chinnusamy V.
Publication year - 2010
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.1647
Subject(s) - chemistry , schiff base , ruthenium , triphenylphosphine , catalysis , ligand (biochemistry) , medicinal chemistry , osmium , polymer chemistry , triphenylarsine , organic chemistry , biochemistry , receptor
The reaction of the Schiff bases (obtained by condensing isatin with o ‐aminophenol/ o ‐aminothiophenol/ o ‐aminobenzoic acid) with [RuX 3 (EPh 3 ) 3 ] (where X = Cl/Br; E = P/As) in benzene afforded new, air‐stable Ru(III) complexes of the general formula [Ru(L)X(EPh 3 ) 2 ] (L = dianion of tridentate Schiff bases). In all these reactions, the Schiff base ligand replaces one triphenylphosphine/triphenylarsine and two chlorides/bromides from the ruthenium precursors. The complexes were characterized by elemental analyses, spectral (FT–IR, UV–vis, 1 H and 13 C NMR for the ligands, and EPR) and electrochemical studies. All the metal complexes exhibit characteristic LMCT absorption bands in the visible region. The catalytic reactivity proved these complexes to be efficient catalysts in the oxidation of alcohols and CC coupling. All the complexes were screened for their biocidal efficiency against bacteria such as Staphylococcus epidermidis and Escherichia coli and fungi such as Botrytis cinerea and Aspergillus niger at 0.25, 0.50 and 1% concentrations. Copyright © 2010 John Wiley & Sons, Ltd.