Abstract
The tauto-merism (Scheme 1) of these ligands as well as the wellknown tendency of sulfur donors to act as bridging ligandsallows various structural possibilities for the correspondingmetal complexes. As part of our studies on the coordination chemistry of d-block metal complexes with schiff base ligands, we haveearlier reported the synthesis and spectroscopic and electro-chemical properties for the dioxomolybdenum(VI) com-plexes, such as [MoO
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