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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 trioxide powder.. Compounds of arsenic resemble in some respects those of phosphorus which occupies the same group (column) of the periodic table.The most common oxidation states for arsenic are: −3 in the arsenides, which are alloy-like intermetallic compounds, +3 in the arsenites, and +5 in the arsenates and most organoarsenic compounds.
[9] [1] One local name used in Bradford—an industrial town in the West Riding of Yorkshire—was "daft". [1] Arsenic trioxide in crystallised form. In the Victorian era, arsenic was an ingredient in several household products, including medicines (for external and internal use), candles, wallpaper, soft furnishings and colourants for foods. [10]
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
Arsenic is a chemical element with the symbol As and the atomic number 33. It is a metalloid and one of the pnictogens, and therefore shares many properties with its group 15 neighbors phosphorus and antimony. Arsenic is a notoriously toxic heavy metal.
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 ...
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]
Bonding in arsenate consists of a central arsenic atom, with oxidation state +5, double bonded to one oxygen atom and single bonded to a further three oxygen atoms. [2] The four oxygen atoms orient around the arsenic atom in a tetrahedral geometry. [2] Resonance disperses the ion's −3 charge across all four oxygen atoms.