The arsenate is an ion with the chemical formula . Bonding in arsenate consists of a central arsenic atom, with oxidation state +5, Double bond to one oxygen atom and Single bond to a further three oxygen atoms. The four oxygen atoms orient around the arsenic atom in a tetrahedral geometry. Resonance disperses the ion's −3 charge across all four oxygen atoms.
Arsenate readily reacts with metals to form arsenate metal compounds. Arsenate is a moderate Oxidant and an electron acceptor, with an electrode potential of +0.56 Volt for its reduction to arsenite. Due to arsenic having the same valency and similar atomic radius to phosphorus, arsenate shares similar geometry and reactivity with phosphate. Arsenate can replace phosphate in Biochemistry and is Toxicity to most Organism.
Transition metal arsenate compounds are often brightly coloured and have been used to make Pigment. Copper arsenate was a minor compound used in the Egyptian blue pigment used by the ancient Egyptians and Ancient Rome. Cobalt violet pigment was made from cobalt arsenate before its toxicity led to its replacement by cobalt phosphate.
Chromated copper arsenate (CCA) has been a widely used wood preservative since the 1930s. Safety concerns have led to the phasing out of CCA-treated wood for Residential area projects in many countries. CCA remains a common and economical treatment choice for non-residential uses such as agriculture.
These values are similar to those of phosphoric acid. Hydrogen arsenate and dihydrogen arsenate predominate in aqueous solution near neutral pH.
The reduction potential (pe) of a solution also affects arsenate speciation. In natural waters, the Dissolved Oxygen is the main factor influencing reduction potential. Arsenates occur in oxygenated waters, which have a high pe, while arsenites are the main arsenic species in anoxic waters with a low pe.
A Pourbaix diagram shows the combined influence of pH and pe on arsenate speciation.
As with other arsenic compounds, arsenate binds to lipoic acid, inhibiting the conversion of pyruvate into acetyl-CoA, blocking the Krebs cycle and therefore resulting in further loss of ATP.
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