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  2. Organoselenium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoselenium_chemistry

    Organoselenium chemistry is the science exploring the properties and reactivity of organoselenium compounds, chemical compounds containing carbon-to-selenium chemical bonds. [1] [2] [3] Selenium belongs with oxygen and sulfur to the group 16 elements or chalcogens, and similarities in chemistry are to be expected. Organoselenium compounds are ...

  3. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbonhydrogen_bond...

    In organic chemistry and organometallic chemistry, carbonhydrogen bond activation (C−H activation) is a type of organic reaction in which a carbonhydrogen bond is cleaved and replaced with a C−X bond (X ≠ H is typically a main group element, like carbon, oxygen, or nitrogen).

  4. Hydrogen selenide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_selenide

    Hydrogen selenide is an inorganic compound with the formula H 2 Se. This hydrogen chalcogenide is the simplest and most commonly encountered hydride of selenium. H 2 Se is a colorless, flammable gas under standard conditions. It is the most toxic selenium compound [3] with an exposure limit of 0.05 ppm over an 8-hour period.

  5. Selenium compounds - Wikipedia

    en.wikipedia.org/wiki/Selenium_compounds

    Selenium forms two oxides: selenium dioxide (SeO 2) and selenium trioxide (SeO 3). Selenium dioxide is formed by the reaction of elemental selenium with oxygen: [5] + It is a polymeric solid that forms monomeric SeO 2 molecules in the gas phase. It dissolves in water to form selenous acid, H 2 SeO 3.

  6. Selenide - Wikipedia

    en.wikipedia.org/wiki/Selenide

    The parent inorganic selenide is hydrogen selenide (H 2 Se). It is a colorless, malodorous, toxic gas. It dissolves in aqueous solution, to give the hydrogenselenide or biselenide ion HSe −. At higher pH, selenide forms. Solutions of hydrogen selenide and selenide are oxidized by air to give elemental selenium: 2 SeH − + O 2 → 2 Se + 2 OH −

  7. Agostic interaction - Wikipedia

    en.wikipedia.org/wiki/Agostic_interaction

    The term agostic is reserved to describe two-electron, three-center bonding interactions between carbon, hydrogen, and a metal. Two-electron three-center bonding is clearly implicated in the complexation of H 2 , e.g., in W(CO) 3 (PCy 3 ) 2 H 2 , which is closely related to the agostic complex shown in the figure. [ 8 ]

  8. Selenoxide elimination - Wikipedia

    en.wikipedia.org/wiki/Selenoxide_elimination

    A second significant side reaction in reactions of ketones and aldehydes is selanylation of the intermediate selenoxide. This process leads to elimination products retaining a carbon-selenium bond, [16] and is more difficult to prevent than the seleno-Pummerer reaction. Tertiary selenoxides, which are unable to undergo enolization, do not react ...

  9. 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.