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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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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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Structural Isomerism02:34

Structural Isomerism

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Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
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Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

48.1K
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 the dxy,...
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Diamagnetism01:26

Diamagnetism

2.9K
Materials consisting of paired electrons have zero net magnetic moments. However, when these materials are placed under an external magnetic field, the moments opposite to the field are induced. Such materials are called diamagnets. Diamagnetism is the response of the diamagnets when placed in an external magnetic field.
Diamagnetism was discovered by Anton Brugmans in 1778 when he observed that bismuth gets repelled by magnetic fields, thus theorizing that diamagnets get repelled by magnets....
2.9K
Formation of Complex Ions03:45

Formation of Complex Ions

25.7K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
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Updated: Jan 15, 2026

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
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A Neutral Dy(II) Bis(amide): Synthesis, Magnetism, and a P42- Complex.

Rashmi Jena1, Florian Benner1, Richard J Staples1

  • 1Department of Chemistry, Michigan State University, 578 S. Shaw Ln, East Lansing, Michigan 48824, United States of America.

Inorganic Chemistry
|October 7, 2025
PubMed
Summary

Researchers synthesized a stable dysprosium(II) complex, Dy(NHAr*)2, a black sandwich compound. This dysprosium(II) complex exhibits a reversible Dy2+/3+ redox couple and reacts with isocyanide and phosphorus molecules.

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Area of Science:

  • Organometallic Chemistry
  • Lanthanide Chemistry
  • Coordination Chemistry

Background:

  • Dysprosium complexes are of interest due to their unique electronic properties.
  • Synthesis of low-valent lanthanide compounds presents significant challenges.
  • Sterically demanding ligands are often employed to stabilize reactive metal centers.

Purpose of the Study:

  • To synthesize and characterize a novel dysprosium(II) complex.
  • To investigate the redox properties of the dysprosium center.
  • To explore the reactivity of the dysprosium(II) complex with small molecules.

Main Methods:

  • Reaction of DyCl3 with KNHAr* ligand precursor.
  • Reduction of Dy(III) intermediate with KC8.
  • Electrochemical analysis to determine redox potential.
  • CASSCF calculations for electronic structure.
  • Reactions with tert-butyl isocyanide and white phosphorus (P4).

Main Results:

  • Formation of a room-temperature stable dysprosium(II) sandwich complex, Dy(NHAr*)2.
  • Determination of a reversible Dy2+/3+ redox potential of -1.094 V vs. FeCp2+/0.
  • CASSCF calculations suggest a 4f95d1 electronic configuration.
  • The Dy(II) complex reacts with CNtBu and P4, yielding isocyanide and polyphosphide complexes, respectively.

Conclusions:

  • A stable dysprosium(II) complex, Dy(NHAr*)2, has been successfully synthesized and characterized.
  • The electronic structure and redox behavior of this complex provide insights into low-valent dysprosium chemistry.
  • The reactivity studies demonstrate the potential of Dy(II) complexes in coordinating small molecules like isocyanides and polyphosphides.