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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

21.6K
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...
21.6K
Coordination Number and Geometry02:57

Coordination Number and Geometry

16.8K
For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
16.8K
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...
12.4K
Valence Bond Theory02:42

Valence Bond Theory

9.8K
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...
9.8K
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

28.1K
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...
28.1K
Ladder Diagrams: Complexation Equilibria01:07

Ladder Diagrams: Complexation Equilibria

434
Ladder diagrams are useful for evaluating equilibria involving metal-ligand complexes. The vertical scale of the ladder diagram represents the concentration of unreacted or free ligand, pL. The horizontal lines on the scale depict the log of stepwise formation constants for metal-ligand complexes and indicate the dominant species in all the regions.
The formation constant, K1, for the formation of Cd(NH3)2+ complex from cadmium and ammonia is 3.55 × 102. Log K1 (i.e. pNH3) is 2.55, and...
434

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Related Experiment Video

Updated: Sep 28, 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

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Conformationally dynamic copper coordination complexes.

Bronte J Charette1, Paul J Griffin1, Claire M Zimmerman1

  • 1Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA. lolshans@illinois.edu.

Dalton Transactions (Cambridge, England : 2003)
|March 31, 2022
PubMed
Summary

Copper complexes with dynamic ligands exhibit tunable redox behavior. This study reveals how ligand conformation influences electron transfer in copper complexes, enabling controlled reactivity.

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Area of Science:

  • Coordination Chemistry
  • Inorganic Chemistry
  • Electron Transfer Studies

Background:

  • The redox properties and reactivity of copper complexes are intrinsically linked to their oxidation states (CuI and CuII) and coordination geometries.
  • Conformationally dynamic chelating ligands offer a pathway to stabilize multiple copper oxidation states, facilitating controlled redox reactions.

Purpose of the Study:

  • To analyze the conformational dynamics of copper(I) complexes with dipicolylaniline (dpaR) ligands.
  • To investigate the relationship between ligand conformation and redox activity in these copper complexes.

Main Methods:

  • Variable temperature Nuclear Magnetic Resonance (NMR) spectroscopy
  • Electrochemical experiments
  • Single crystal X-ray diffraction
  • Electron Paramagnetic Resonance (EPR) spectroscopy

Main Results:

  • An equilibrium between two distinct conformers (planar and tetrahedral) was observed in solution at room temperature for CuI complexes.
  • Two metal-centered redox events were identified, corresponding to the CuII/I couple in these different conformations.
  • Activation and equilibrium parameters for the interconversion between conformations were determined.

Conclusions:

  • The conformational dynamics of dipicolylaniline ligands play a crucial role in the redox behavior of copper complexes.
  • Understanding and controlling these redox-triggered conformational changes provides opportunities for designing novel copper-based electron transfer systems.