When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Selenosulfide - Wikipedia

    en.wikipedia.org/wiki/Selenosulfide

    Simplest is the material selenium sulfide, which has medicinal properties. It adopt the diverse structures of elemental sulfur but with some S atoms replaced by Se. Other inorganic selenide sulfide compounds occur as minerals and as pigments. One example is antimony selenosulfide. The pigment cadmium red consists of cadmium sulfoselenide.

  3. Selenium compounds - Wikipedia

    en.wikipedia.org/wiki/Selenium_compounds

    The sulfoxide in sulfur chemistry is represented in selenium chemistry by the selenoxides (formula RSe(O)R), which are intermediates in organic synthesis, as illustrated by the selenoxide elimination reaction. Consistent with trends indicated by the double bond rule, selenoketones, R(C=Se)R, and selenaldehydes, R(C=Se)H, are rarely observed.

  4. Selenium - Wikipedia

    en.wikipedia.org/wiki/Selenium

    Selenium is found in metal sulfide ores, where it substitutes for sulfur. Commercially, selenium is produced as a byproduct in the refining of these ores. Minerals that are pure selenide or selenate compounds are rare. The chief commercial uses for selenium today are glassmaking and pigments. Selenium is a semiconductor and is used in photocells.

  5. Selenium sulfide - Wikipedia

    en.wikipedia.org/wiki/Selenium_sulfide

    Download as PDF; Printable version; In other projects ... move to sidebar hide. Selenium sulfide can refer to either of the following : Selenium disulfide, SeS 2 ...

  6. Sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Sulfoxide

    Enantiomers of methyl phenyl sulfoxide. A lone pair of electrons resides on the sulfur atom, giving it tetrahedral electron-pair geometry and trigonal pyramidal shape (steric number 4 with one lone pair; see VSEPR theory). When the two organic residues are dissimilar, the sulfur atom is a chiral center, for example, in methyl phenyl sulfoxide.

  7. Selenoxide elimination - Wikipedia

    en.wikipedia.org/wiki/Selenoxide_elimination

    Selenium in these reactions is almost always stereogenic, and the effect of epimerization at selenium (which is acid-catalyzed and occurs readily) on the elimination reaction is nearly unknown. In one example, separation and warming of selenoxides 1 and 2 revealed that 2 decomposes at 0 °C, while 1 , which presumably has more difficulty ...

  8. Organoselenium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoselenium_chemistry

    Selones (R 2 C=Se) are the selenium analogues of ketones. They are rare due to their tendency to oligomerize. [11] Diselenobenzoquinone is stable as a metal complex. [12] Selenourea is an example of a stable compound containing a C=Se bond. Thioselenides (R−Se−S−R), compounds with selenium(II)–sulfur(II) bonds, analogous to disulfides.

  9. Transition metal sulfoxide complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_sulfoxide...

    Being weakly basic, sulfoxide ligands are generally labile, i.e. they are rapidly displaced by other more basic ligands. O-bonded sulfoxide ligands are susceptible to oxidation at sulfur. In this way, the weakly bonded ligand is converted into a leaving group, such as dimethylsulfone. Since dmso is susceptible to deprotonation by strong base ...