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  2. Germanium dichloride - Wikipedia

    en.wikipedia.org/wiki/Germanium_dichloride

    The structure of gas-phase molecular GeCl 2 shows that it is a bent molecule, as predicted by VSEPR theory. [5] The dioxane complex, GeCl 2 ·dioxane, has been used as a source of molecular GeCl 2 for reaction syntheses, as has the in situ reaction of GeCl 4 and Ge metal. GeCl 2 is quite reactive and inserts into many types of chemical bonds. [6]

  3. Germanium dichloride dioxane - Wikipedia

    en.wikipedia.org/wiki/Germanium_dichloride_dioxane

    It is prepared by reduction of a dioxane solution of germanium tetrachloride with tributyltin hydride: [2]. GeCl 4 + 2 Bu 3 SnH + C 4 H 8 O 2 → GeCl 2 (O 2 C 4 H 8) + 2 Bu 3 SnCl + H 2

  4. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    A diatomic molecular orbital diagram is used to understand the bonding of a diatomic molecule. MO diagrams can be used to deduce magnetic properties of a molecule and how they change with ionization. They also give insight to the bond order of the molecule, how many bonds are shared between the two atoms. [12]

  5. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    In chemistry, orbital hybridisation (or hybridization) is the concept of mixing atomic orbitals to form new hybrid orbitals (with different energies, shapes, etc., than the component atomic orbitals) suitable for the pairing of electrons to form chemical bonds in valence bond theory.

  6. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    In chemistry, isovalent or second order hybridization is an extension of orbital hybridization, the mixing of atomic orbitals into hybrid orbitals which can form chemical bonds, to include fractional numbers of atomic orbitals of each type (s, p, d). It allows for a quantitative depiction of bond formation when the molecular geometry deviates ...

  7. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    This is a weighted sum of the wavefunctions. Now choose a second hybrid orbital s + √ λ j p j, where p j is directed in some way and λ j is the amount of p character in this second orbital. The value of λ j and direction of p j must be determined so that the resulting orbital can be normalized and so that it is orthogonal to the first ...

  8. Orbital overlap - Wikipedia

    en.wikipedia.org/wiki/Orbital_overlap

    In chemical bonds, an orbital overlap is the concentration of orbitals on adjacent atoms in the same regions of space. Orbital overlap can lead to bond formation. Linus Pauling explained the importance of orbital overlap in the molecular bond angles observed through experimentation; it is the basis for orbital hybridization.

  9. Lone pair - Wikipedia

    en.wikipedia.org/wiki/Lone_pair

    The s character rich O σ(out) lone pair orbital (also notated n O (σ)) is an ~sp 0.7 hybrid (~40% p character, 60% s character), while the p lone pair orbital (also notated n O (π)) consists of 100% p character. Both models are of value and represent the same total electron density, with the orbitals related by a unitary transformation.