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Related Concept Videos

Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

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Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than...
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Valence Bond Theory02:42

Valence Bond Theory

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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...
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Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

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Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
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Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

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Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
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Colors and Magnetism03:02

Colors and Magnetism

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Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
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Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

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The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
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Updated: Apr 16, 2026

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
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Interference enhanced thermoelectricity in quinoid type structures.

M Strange1, J S Seldenthuis2, C J O Verzijl2

  • 1Nano-Science Center and Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, Denmark.

The Journal of Chemical Physics
|March 2, 2015
PubMed
Summary
This summary is machine-generated.

Quinoid molecules exhibit quantum interference for enhanced thermoelectricity. Chemical modifications tune these effects, leading to high performance in thermoelectric devices.

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Area of Science:

  • Molecular electronics
  • Quantum phenomena in materials
  • Thermoelectric energy conversion

Background:

  • Quantum interference (QI) in molecular junctions offers potential for significant thermoelectric effects.
  • Understanding molecular structures that optimize thermoelectric properties is crucial for device development.

Purpose of the Study:

  • To investigate quantum interference effects in quinoid-based molecular junctions.
  • To explore the tunability of thermoelectric properties through chemical modifications of molecular structures.

Main Methods:

  • Utilizing density functional theory (DFT) to study electrical conductance (G) and thermoelectric response.
  • Employing a semi-empirical interacting model Hamiltonian with the GW approximation for the molecular π-system.

Main Results:

  • Quinoid molecules display two distinct destructive QI features near frontier orbital energies, appearing as transmission dips.
  • These QI features remain separated despite the addition of electron-donating or withdrawing side groups.
  • Transmission dip positions and frontier molecular levels are chemically controllable via side groups and conjugation length.

Conclusions:

  • Quinoid molecules possess tunable quantum interference, enabling control over thermoelectric properties.
  • The ability to chemically tune these molecules results in high thermoelectric power factors and figures of merit (ZT).
  • Quinoid-based molecular systems show promise for efficient thermoelectric device applications.