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Arsenic (III) binding sites usually use thiol groups of cysteine residues. The catalysis involves thiolates of Cys72, Cys174, and Cys224. In an SN2 reaction, the positive charge on the SAM sulfur atom pulls the bonding electron from the carbon of the methyl group, which interacts with the arsenic lone pair to form an As−C bond, leaving SAH. [31]
Arsenic forms colorless, odorless, crystalline oxides As 2 O 3 ("white arsenic") and As 2 O 5 which are hygroscopic and readily soluble in water to form acidic solutions. Arsenic(V) acid is a weak acid and the salts are called arsenates , [ 5 ] the most common arsenic contamination of groundwater , and a problem that affects many people.
From one acute exposure, someone who has inhaled lewisite can develop chronic respiratory disease; eye exposure to lewisite can cause permanent visual impairment or blindness. [ 5 ] Chronic exposure to lewisite can cause arsenic poisoning (due to its arsenic content) and development of a lewisite allergy .
Bioremediation of ground water contaminated with arsenic aims to convert arsenite, the toxic form of arsenic to humans, to arsenate. Arsenate (+5 oxidation state) is the dominant form of arsenic in surface water, while arsenite (+3 oxidation state) is the dominant form in hypoxic to anoxic environments.
In its standard state arsine is a colorless, denser-than-air gas that is slightly soluble in water (2% at 20 °C) [1] and in many organic solvents as well. [citation needed] Arsine itself is odorless, [5] but it oxidizes in air and this creates a slight garlic or fish-like scent when the compound is present above 0.5 ppm. [6]
Arsenic-arsenic bonds are very weak, and oligomeric arsenic compounds are even more liable to oxidize than their hydrogenated precursors. [6]: 318–320 The following reaction can, however, be prepared through electrochemical reduction in a zinc-sulfate cell. [6]: 473 Oxidation first forms polymeric arsinoxides, e.g.: MeAs + O → MeAsO
Cummins' Mo(N(tBu)Ar) 3 catalyst, also known to split the N-N triple bond in dinitrogen, reacts with yellow arsenic to form a terminal arsenic moiety triple-bonded to the metal center - one of only several compounds known to contain a terminal arsenic atom. [15] Complexes with metal-metal multiple bonds also enable mild As 4 activation ...
Phosphorous acid exists as the dihydroxy tautomer in contrast to arsenous acid.. As(OH) 3 is a pyramidal molecule consisting of three hydroxyl groups bonded to arsenic. The 1 H NMR spectrum of arsenous acid solutions consists of a single signal consistent with the molecule's high symmetry. [3]