In chelate complexes the metal ion performs a coordination with two or more donor atoms of the same ligand. The chelate impact means preferring metal ions in order to create complexes with chelating ligand instead of non-chelating ones in which the two types of ligands are capable of forming bonds of similar strength. The impact of the chelate is influenced by the effects of enthalpy and entropy [1]. Metal complexes of oxygen, sulfur and nitrogen-chelating ligands gained consideration owing to their curiously explanatory [2], biological [3] and physico-chemical [4], properties, articulated biological activities and for their utility as models of metalloenzyme dynamic sites [5]. In coordination of metals, sulfur and nitrogen atoms play a key part at the dynamic destinations of various metallobimolecules [6]. The intrigued in sulfur given chelating operators have developed exceptionally rapidly [7]. Coordination chemistry is centered on potential applications of macrocylic thio Schiff bases and their metal complexes [8]. Dithiocarbamates are very common compounds binding strongly and selectively to a wide range of metal ions, therefore, in the past decade self-assembly which is controlled by the MINI REVIEW Metal Complexes of Dithiocarbamate Derivatives and its Biological Activity