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  2. Beryllium fluoride - Wikipedia

    en.wikipedia.org/wiki/Beryllium_fluoride

    Molecular BeF 2 in the gaseous state is isoelectronic to carbon dioxide. As a liquid, beryllium fluoride has a tetrahedral structure. The density of liquid BeF 2 decreases near its freezing point, as Be 2+ and F − ions begin to coordinate more strongly with one another, leading to the expansion of voids between formula units. [11]

  3. Linear molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Linear_molecular_geometry

    The linear molecular geometry describes the geometry around a central atom bonded to two other atoms (or ligands) placed at a bond angle of 180°. Linear organic molecules, such as acetylene (HC≡CH), are often described by invoking sp orbital hybridization for their carbon centers. Two sp orbitals

  4. Tetrafluoroberyllate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroberyllate

    The gas above molten sodium tetrafluoroberyllate contains BeF 2 and NaF gas. [11] Lithium tetrafluoroberyllate takes on the same crystal form as the mineral phenacite. As a liquid it is proposed for the molten salt reactor, in which it is called FLiBe. The liquid salt has a high specific heat, similar to that of water.

  5. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The fluorine–fluorine bond of the difluorine molecule is relatively weak when compared to the bonds of heavier dihalogen molecules. The bond energy is significantly weaker than those of Cl 2 or Br 2 molecules and similar to the easily cleaved oxygen–oxygen bonds of peroxides or nitrogen–nitrogen bonds of hydrazines. [8]

  6. Organoberyllium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoberyllium_chemistry

    The structure of dimethylberyllium. The coordination number of Be in organoberyllium compounds ranges from two to four. [4] Dimethylberyllium and dimethylmagnesium adopts the same structure. [5] Diethylberyllium, however, does not structurally resemble diethylmagnesium (which has the same structure as dimethylmagnesium). [6]

  7. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...

  8. Covalent bond - Wikipedia

    en.wikipedia.org/wiki/Covalent_bond

    A covalent bond forming H 2 (right) where two hydrogen atoms share the two electrons. A covalent bond is a chemical bond that involves the sharing of electrons to form electron pairs between atoms. These electron pairs are known as shared pairs or bonding pairs.

  9. Beryllium hydride - Wikipedia

    en.wikipedia.org/wiki/Beryllium_hydride

    Structure of gaseous BeH 2. Isolated molecules of BeH 2 (sometimes called dihydridoberyllium and written [BeH 2] to emphasize the differences with the solid state) are only stable as a dilute gas. When condensed, unsolvated BeH 2 will spontaneously autopolymerise.