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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

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The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
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Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

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In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
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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...
10.5K
Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

684
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
684
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...
29.5K
Extraction: Advanced Methods00:56

Extraction: Advanced Methods

903
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
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Related Experiment Video

Updated: Dec 5, 2025

Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR
14:44

Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR

Published on: December 16, 2013

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Not Completely Innocent: How Argon Binding Perturbs Cationic Copper Clusters.

Zahra Jamshidi1,2, Olga V Lushchikova3, Joost M Bakker4

  • 1Chemistry Department, Sharif University of Technology, Tehran 11155-9516, Iran.

The Journal of Physical Chemistry. A
|October 15, 2020
PubMed
Summary
This summary is machine-generated.

Argon probes may alter copper cluster structures. Charge transfer from argon to copper ions affects subsequent argon binding, generally weakening it, except for single copper ions where it enhances binding.

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Area of Science:

  • Physical Chemistry
  • Computational Chemistry
  • Atomic and Molecular Physics

Background:

  • Argon is commonly used as an inert probe in structural studies.
  • The assumption of minimal perturbation by argon is widely accepted.
  • The behavior of argon with small metal cationic clusters is less understood.

Purpose of the Study:

  • To investigate the validity of argon as an innocent probe for copper cationic clusters.
  • To understand how argon interaction influences the binding of other argon atoms to copper clusters.
  • To determine the specific effects of charge transfer on cluster-argon interactions.

Main Methods:

  • Computational modeling of small copper cationic clusters.
  • Simulations of argon atom adsorption and binding energies.
  • Analysis of charge transfer dynamics between argon and copper ions.

Main Results:

  • Argon attachment leads to significant charge transfer to copper cations.
  • This charge transfer alters the electronic structure, affecting other argon binding sites.
  • Generally, subsequent argon atoms bind less strongly, with an exception for single copper ions.

Conclusions:

  • Argon is not always an innocent probe for small copper cationic clusters.
  • Charge transfer effects must be considered when interpreting argon-based structural studies.
  • The interaction is complex, with unique behavior observed for single copper ions.