Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

VSEPR Theory and the Effect of Lone Pairs04:01

VSEPR Theory and the Effect of Lone Pairs

40.0K
Effect of Lone Pairs of Electrons on Molecule Geometry
40.0K
VSEPR Theory and the Basic Shapes02:52

VSEPR Theory and the Basic Shapes

61.8K
Overview of VSEPR Theory
61.8K
VSEPR Theory02:37

VSEPR Theory

11.0K
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...
11.0K
Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

51.5K
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...
51.5K
Predicting Molecular Geometry02:27

Predicting Molecular Geometry

35.6K
VSEPR Theory for Determination of Electron Pair Geometries
35.6K
Valence Bond Theory02:42

Valence Bond Theory

8.8K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
8.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Concordant Mode Approach (CMA): Vibrational Analysis of New and Upgraded Intermolecular Benchmarks for Noncovalent Bonding.

The journal of physical chemistry. A·2026
Same author

Tests of the DFT Ladder for the Fulminic Acid Challenge.

Journal of the American Chemical Society·2025
Same author

Convergent Concordant Mode Approach for Molecular Vibrations: CMA-2.

Journal of chemical theory and computation·2024
Same author

Fulminic acid: a quasibent spectacle.

Physical chemistry chemical physics : PCCP·2024
Same author

Correction: Pericyclic reaction benchmarks: hierarchical computations targeting CCSDT(Q)/CBS and analysis of DFT performance.

Physical chemistry chemical physics : PCCP·2024
Same author

The multichannel i-propyl + O2 reaction system: A model of secondary alkyl radical oxidation.

The Journal of chemical physics·2023
Same journal

On the Nonparametric Diabatization of Coupled Electronic States.

The journal of physical chemistry. A·2026
Same journal

Stability of Some Ternary 13-Atom Icosahedral Clusters Assessed with Geometric, Electronic, and Thermodynamic Criteria.

The journal of physical chemistry. A·2026
Same journal

A Three-Phase Distribution Method for Quantifying the Intermolecular Interactions.

The journal of physical chemistry. A·2026
Same journal

Cooperative Effects in the Inverse Coordination Complexes of Aromatic Azines and Tin(IV) Halides.

The journal of physical chemistry. A·2026
Same journal

The Infrared Spectra of Neutral Dimethyl-Sulfide, -Disulfide and -Sulfoxide Biomarkers in Molecular Beams.

The journal of physical chemistry. A·2026
Same journal

Photoinduced Charge-Transfer Suppresses Triplet Formation Efficiency in Thiocoumarins: Evidence from Ultrafast Spectroscopy and Theoretical Calculations.

The journal of physical chemistry. A·2026
See all related articles

Related Experiment Video

Updated: Apr 22, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
06:35

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates

Published on: February 15, 2016

7.5K

Bond angles around a tetravalent atom.

Robert K Bohn1, Wesley D Allen

  • 1Department of Chemistry, University of Connecticut , Storrs, Connecticut 06269-3060, United States.

The Journal of Physical Chemistry. A
|October 8, 2014
PubMed
Summary
This summary is machine-generated.

The symmetry of a central atom dictates the relationships between its bond angles. As symmetry decreases, the number of independent bond angles increases, offering greater molecular flexibility.

More Related Videos

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

71.2K
Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
08:54

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid

Published on: January 25, 2020

5.0K

Related Experiment Videos

Last Updated: Apr 22, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
06:35

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates

Published on: February 15, 2016

7.5K
From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

71.2K
Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
08:54

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid

Published on: January 25, 2020

5.0K

Area of Science:

  • Chemistry
  • Molecular Geometry
  • Symmetry Analysis

Background:

  • The arrangement of atoms in molecules is governed by bond angles.
  • The symmetry of a molecule significantly influences these bond angles.

Purpose of the Study:

  • To derive exact mathematical relationships between bond angles based on molecular symmetry.
  • To explore how symmetry reduction impacts the degrees of freedom in bond angles.

Main Methods:

  • Algebraic treatment of mathematical conditions for bond angles.
  • Factorization of conditions based on symmetry constraints.
  • Geometric analysis starting from high symmetry (Td) and reducing stepwise.

Main Results:

  • Established exact relationships between six bond angles around a central tetravalent atom.
  • Demonstrated that degrees of freedom increase from zero to five as symmetry decreases from Td to C1.
  • Provided a systematic mathematical framework for understanding angle variations.

Conclusions:

  • Molecular symmetry is a key determinant of bond angle relationships.
  • Lowering symmetry increases the independent variations possible in bond angles.
  • The derived formulas offer a quantitative understanding of geometric flexibility in molecules.