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  2. Hydride - Wikipedia

    en.wikipedia.org/wiki/Hydride

    The hydride reacts with the weak Bronsted acid releasing H 2. Hydrides such as calcium hydride are used as desiccants, i.e. drying agents, to remove trace water from organic solvents. The hydride reacts with water forming hydrogen and hydroxide salt. The dry solvent can then be distilled or vacuum transferred from the "solvent pot".

  3. Transition metal hydride - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_hydride

    The reaction involves no changes in the oxidation state of the metal and can be viewed as splitting H 2 into hydride (which binds to the metal) and proton (which binds to the base). ML n x+ + base + H 2 ⇌ HML n (x-1)+ + Hbase + Such reaction are assumed to involve the intermediacy of dihydrogen complexes. Bifunctional catalysts activate H 2 ...

  4. Binary compounds of hydrogen - Wikipedia

    en.wikipedia.org/wiki/Binary_compounds_of_hydrogen

    Binary hydrogen compounds in group 1 are the ionic hydrides (also called saline hydrides) wherein hydrogen is bound electrostatically. Because hydrogen is located somewhat centrally in an electronegative sense, it is necessary for the counterion to be exceptionally electropositive for the hydride to possibly be accurately described as truly behaving ionic.

  5. Hydrogen-moderated self-regulating nuclear power module

    en.wikipedia.org/wiki/Hydrogen-moderated_self...

    This was tried in operation Upshot–Knothole, [7] where hydrogen was used to reduce the critical mass. The test explosions codenamed Ruth and Ray used in the core uranium hydride. Ruth used the hydrogen isotope protium (1 H) and Ray used the hydrogen isotope deuterium (2 H or 2 D) as neutron moderators. The predicted yield was 1.5 to 3 kt TNT ...

  6. Ionic hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Ionic_hydrogenation

    One hydride serves as the hydride source, and the other serves as a proton source. [2] In the case of ionic hydrogenation, a dihydride complex is regenerated by hydrogen gas following hydrogenation. Typical catalysts are tungsten or molybdenum complexes. An example of such a catalyst is CpMo(CO) 2 (PR 3)(OCR' 2)]+ where M = W or Mo. [7]

  7. Hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation

    The transition state of two transfer-hydrogenation reactions from ruthenium-hydride complexes onto carbonyls. Transfer hydrogenation uses hydrogen-donor molecules other than molecular H 2. These "sacrificial" hydrogen donors, which can also serve as solvents for the reaction, include hydrazine, formic acid, and alcohols such as isopropanol. [18]

  8. Magnesium hydride - Wikipedia

    en.wikipedia.org/wiki/Magnesium_hydride

    MgH 2 readily reacts with water to form hydrogen gas: MgH 2 + 2 H 2 O → 2 H 2 + Mg(OH) 2. At 287 °C it decomposes to produce H 2 at 1 bar pressure. [16] The high temperature required is seen as a limitation in the use of MgH 2 as a reversible hydrogen storage medium: [17] MgH 2 → Mg + H 2

  9. Magnesium monohydride - Wikipedia

    en.wikipedia.org/wiki/Magnesium_monohydride

    An electric discharge through hydrogen gas at low pressure (20 pascals) containing pieces of magnesium can produce MgH. [7] Thermally produced hydrogen atoms and magnesium vapour can react and condense in a solid argon matrix. This process does not work with solid neon, probably due to the formation of MgH 2 instead. [8]