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Selenium can exist with oxidation state −2, +2, +4, +6. Se(II) is the dominant form in organoselenium chemistry. Se(II) is the dominant form in organoselenium chemistry. Down the group 16 column, the bond strength becomes increasingly weaker (234 kJ / mol for the C−Se bond and 272 kJ/mol for the C−S bond) and the bond lengths longer ( C ...
Selenium trioxide may be synthesized by dehydrating selenic acid, H 2 SeO 4, which is itself produced by the oxidation of selenium dioxide with hydrogen peroxide: [26] SeO 2 + H 2 O 2 → H 2 SeO 4 Hot, concentrated selenic acid reacts with gold to form gold(III) selenate.
Whereas SO 2 tends to be molecular and SeO 2 is a one-dimensional chain, TeO 2 is a cross-linked polymer. [5] SeO 2 is considered an acidic oxide: it dissolves in water to form selenous acid. [6] Often the terms selenous acid and selenium dioxide are used interchangeably. It reacts with base to form selenite salts containing the SeO 2− 3 anion.
The isotope selenium-75 has radiopharmaceutical uses. For example, it is used in high-dose-rate endorectal brachytherapy, as an alternative to iridium-192. [8]In paleobiogeochemistry, the ratio in amount of selenium-82 to selenium-76 (i.e, the value of δ 82/76 Se) can be used to track down the redox conditions on Earth during the Neoproterozoic era in order to gain a deeper understanding of ...
Phosphorus - selenium glasses have been examined using 31 P-NMR and Raman spectroscopy. Glasses are formed in P x Se 1− x over the range of compositions 0 < x < 0.8 with a small window around 0.52 – 0.60 centred on 0.57 (corresponding to the compound P 4 Se 3 ) where there is a tendency to crystallise.
Selenocysteine is an analogue of the more common cysteine with selenium in place of the sulfur. Selenocysteine is present in several enzymes (for example glutathione peroxidases , tetraiodothyronine 5′ deiodinases , thioredoxin reductases , formate dehydrogenases , glycine reductases , selenophosphate synthetase 2 , methionine- R -sulfoxide ...
In the decade that ensued, selenium-mediated oxidation rapidly expanded in use, and in 1939, Andre Guillemonat and co-workers disclosed the selenium dioxide-mediated oxidation of olefins at the allylic position. [2] Today, selenium-dioxide-mediated oxidation of methylene groups to alpha ketones and at the allylic position of olefins is known as ...