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  2. 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 ...

  3. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    To summarize, we are assuming that: (1) the energy of an electron in an isolated C(2p z) orbital is =; (2) the energy of interaction between C(2p z) orbitals on adjacent carbons i and j (i.e., i and j are connected by a σ-bond) is =; (3) orbitals on carbons not joined in this way are assumed not to interact, so = for nonadjacent i and j; and ...

  4. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    the molecule must be (close to) planar (p orbitals must be roughly parallel and able to interact, implicit in the requirement for conjugation); the molecule must be cyclic (as opposed to linear); the molecule must have a continuous ring of p atomic orbitals (there cannot be any sp 3 atoms in the ring, nor do exocyclic p orbitals count).

  5. Atomic orbital - Wikipedia

    en.wikipedia.org/wiki/Atomic_orbital

    The p z orbital is the same as the p 0 orbital, but the p x and p y are formed by taking linear combinations of the p +1 and p1 orbitals (which is why they are listed under the m = ±1 label). Also, the p +1 and p1 are not the same shape as the p 0, since they are pure spherical harmonics.

  6. Localized molecular orbitals - Wikipedia

    en.wikipedia.org/wiki/Localized_molecular_orbitals

    Localized molecular orbitals are molecular orbitals which are concentrated in a limited spatial region of a molecule, such as a specific bond or lone pair on a specific atom. They can be used to relate molecular orbital calculations to simple bonding theories, and also to speed up post-Hartree–Fock electronic structure calculations by taking ...

  7. Ligand field theory - Wikipedia

    en.wikipedia.org/wiki/Ligand_field_theory

    The metal also has six valence orbitals that span these irreducible representations - the s orbital is labeled a 1g, a set of three p-orbitals is labeled t 1u, and the d z 2 and d x 2 −y 2 orbitals are labeled e g. The six σ-bonding molecular orbitals result from the combinations of ligand SALCs with metal orbitals of the same symmetry. [8]

  8. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The oxygen atomic orbitals are labeled according to their symmetry as a 1 for the 2s orbital and b 1 (2p x), b 2 (2p y) and a 1 (2p z) for the three 2p orbitals. The two hydrogen 1s orbitals are premixed to form a 1 (σ) and b 2 (σ*) MO. Mixing takes place between same-symmetry orbitals of comparable energy resulting a new set of MO's for water:

  9. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    For four atoms bonded together in a chain, the torsional angle is the angle between the plane formed by the first three atoms and the plane formed by the last three atoms. There exists a mathematical relationship among the bond angles for one central atom and four peripheral atoms (labeled 1 through 4) expressed by the following determinant.