The manipulation of phosphate ester linkages is very important in the chemistry of life. Cells possess highly evolved enzymatic machinery to make and break these linkages, which are otherwise extremely stable at physiological pH. Selected nucleases and phosphatases, for example, are capable of accelerating the rate of hydrolysis of specific P-O bonds by factors of up to 10(16) and 10(21), respectively. Over the past few decades, chemists have sought to develop low-molecular weight synthetic mimics of such enzymes, not only to help to improve our fundamental understanding of mechanistic aspects of enzyme action, but also with a view to developing new biotechnological tools (artificial restriction enzymes and footprinting agents) and nucleic acid-targetting therapeutics. This review focuses on research undertaken over the past few decades which has sought to mimic the hydrolytic action of metal-containing nucleases with synthetic transition metal complexes that cleave through a hydrolytic mechanism. It concentrates primarily on copper(II), zinc(II) and nickel(II) complexes and traces the evolution of such complexes from simple monomeric systems capable of hydrolysing activated phosphate esters, to the more sophisticated designs that mimic aspects of the cooperative interplay between metal ions, key amino acid residues and microenvironmental effects employed by metallo-nucleases and -phosphatases to achieve their remarkable catalytic efficiencies.
Desbouis, D., Troitsky, I. P., Belousoff, M. J., Spiccia, L., & Graham, B. (2012). Copper(II), zinc(II) and nickel(II) complexes as nuclease mimetics. Coordination Chemistry Reviews, 256(11-12), 897 - 937. https://doi.org/10.1016/j.ccr.2011.12.005