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Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
Hybridization of Atomic Orbitals II03:35

Hybridization of Atomic Orbitals II

sp3d and sp3d 2 Hybridization
Valence Bond Theory and Hybridized Orbitals02:38

Valence Bond Theory and Hybridized Orbitals

According to valence bond theory, a covalent bond results when: (1) an orbital on one atom overlaps an orbital on a second atom, and (2) the single electrons in each orbital combine to form an electron pair. The strength of a covalent bond depends on the extent of overlap of the orbitals involved. Maximum overlap is possible when the orbitals overlap on a direct line between the two nuclei.
A σ bond (single bond in a Lewis structure) is a covalent bond in which the electron density is...
Molecular Orbital Theory II03:51

Molecular Orbital Theory II

Molecular Orbital Energy Diagrams
¹H NMR: Long-Range Coupling01:27

¹H NMR: Long-Range Coupling

The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene π orbitals.
Resonance and Hybrid Structures02:16

Resonance and Hybrid Structures

According to the theory of resonance, if two or more Lewis structures with the same arrangement of atoms can be written for a molecule, ion, or radical, the actual distribution of electrons is an average of that shown by the various Lewis structures.
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.

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Related Experiment Video

Updated: Jun 28, 2026

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
12:11

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry

Published on: April 8, 2020

Range separation and local hybridization in density functional theory.

Thomas M Henderson1, Benjamin G Janesko, Gustavo E Scuseria

  • 1Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005-1892, USA.

The Journal of Physical Chemistry. A
|November 14, 2008
PubMed
Summary

This study reviews novel density functional theory (DFT) exchange-correlation functionals. New flexible functionals aim to improve accuracy and reduce empirical parameters for modeling molecular properties.

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Last Updated: Jun 28, 2026

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Area of Science:

  • Computational chemistry
  • Quantum mechanics
  • Materials science

Background:

  • Kohn-Sham density functional theory (DFT) is standard for modeling molecular properties.
  • Hybrid functionals improve accuracy but have limitations and empirical parameters.
  • Accurate modeling of large molecules and solids is computationally demanding.

Purpose of the Study:

  • To review the development of novel exchange-correlation functionals in DFT.
  • To explore flexible functional forms like local and range-separated hybrids.
  • To construct functionals obeying exact constraints with minimal empirical parametrization.

Main Methods:

  • Developing novel exchange-correlation functionals.
  • Focusing on local and range-separated hybrid functional forms.
  • Ensuring functionals adhere to known exact constraints.

Main Results:

  • Global hybrids have successes but also failures and empirical parameters.
  • Novel functionals offer more flexibility and aim for reduced parametrization.
  • The work is contextualized with other new approximate density functionals.

Conclusions:

  • New DFT functionals are being developed to overcome limitations of existing methods.
  • Flexibility and adherence to exact constraints are key for improved accuracy.
  • Future work will focus on further refining these novel functionals.