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Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

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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...
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¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)01:20

¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)

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When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
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Potential Due to a Polarized Object01:29

Potential Due to a Polarized Object

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A neutral atom consists of a positively charged nucleus surrounded by a negatively charged electron cloud. When placed in an external electric field, the external electric force pulls the electrons and nucleus apart, opposite to the intrinsic attraction between the nucleus and the electrons. The opposing forces balance each other with a slight shift between the center of masses of the nucleus and the electron cloud, resulting in a polarized atom. On the other hand, a few molecules, like water,...
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π Molecular Orbitals of 1,3-Butadiene01:24

π Molecular Orbitals of 1,3-Butadiene

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Conjugated dienes have lower heats of hydrogenation than cumulated and isolated dienes, making them more stable. The enhanced stabilization of conjugated systems can be understood from their π molecular orbitals.
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
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Valence Bond Theory and Hybridized Orbitals02:38

Valence Bond Theory and Hybridized Orbitals

33.0K
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...
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VSEPR Theory02:37

VSEPR Theory

15.8K
Valence shell electron-pair repulsion theory (VSEPR theory) enables us to predict the molecular structure around a central atom from an examination of the number of bonds and lone electron pairs in its Lewis structure. The VSEPR model assumes that electron pairs in the valence shell of a central atom will adopt an arrangement that minimizes repulsions between these electron pairs by maximizing the distance between them. The electrons in the valence shell of a central atom form either bonding...
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Related Experiment Video

Updated: Mar 30, 2026

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
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Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry

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Unifying General and Segmented Contracted Basis Sets. Segmented Polarization Consistent Basis Sets.

Frank Jensen1

  • 1Department of Chemistry, Aarhus University , DK-8000 Aarhus, Denmark.

Journal of Chemical Theory and Computation
|November 19, 2015
PubMed
Summary
This summary is machine-generated.

We introduce P-orthogonalization, a method to create efficient segmented contracted basis sets from general contracted ones without losing accuracy. This enhances computational chemistry for density functional theory calculations.

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Area of Science:

  • Computational Chemistry
  • Quantum Chemistry
  • Theoretical Chemistry

Background:

  • General contracted (GC) basis sets offer high accuracy but can be computationally expensive.
  • Existing methods for basis set manipulation may involve trade-offs between efficiency and accuracy.
  • Density Functional Theory (DFT) calculations require accurate and efficient basis sets for reliable results.

Purpose of the Study:

  • To develop a method (P-orthogonalization) for converting general contracted basis sets into computationally efficient segmented contracted basis sets.
  • To ensure the converted basis sets retain the full accuracy of the original general contracted basis sets.
  • To construct and evaluate a new series of polarization consistent basis sets (pcs-n) for DFT.

Main Methods:

  • The P-orthogonalization procedure is applied to remove redundancies between general contracted functions.
  • The method is used to create segmented contracted versions of polarization consistent basis sets.
  • Benchmark calculations are performed using various exchange-correlation functionals and molecular systems (H-Kr).

Main Results:

  • The P-orthogonalization method successfully converts GC basis sets to segmented contracted forms with preserved accuracy.
  • The new pcs-n basis sets demonstrate uniform error control for basis set incompleteness across diverse molecular systems and DFT functionals.
  • pcs-n basis sets exhibit lower basis set errors compared to existing sets at equivalent zeta quality and offer high computational efficiency.

Conclusions:

  • P-orthogonalization provides an effective strategy for generating accurate and efficient segmented contracted basis sets.
  • The pcs-n basis sets offer a superior balance of accuracy, error control, and computational cost for DFT.
  • The pcs-n basis sets are suitable for both routine and high-level benchmark DFT calculations across a range of chemical systems.