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Valence Bond Theory02:42

Valence Bond Theory

10.7K
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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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

23.3K
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...
23.3K
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

29.9K
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...
29.9K
Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

47.2K
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,...
47.2K
Colors and Magnetism03:02

Colors and Magnetism

13.5K
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...
13.5K
EDTA: Chemistry and Properties01:22

EDTA: Chemistry and Properties

3.0K
Polydentate ligands are most widely used in complexometric titrations because they form more stable complexes with the metal ions than mono- or bidentate ligands due to the chelate effect. Examples of polydentate ligands are ethylenediaminetetraacetic acid (EDTA), crown ethers, and cryptands. The most important feature of optimal polydentate ligands is the ability to form 1:1 complexes in a single-step process. Amino carboxylic acid derivatives are frequently used as complexing agents. EDTA is...
3.0K

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Updated: Dec 10, 2025

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
05:33

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications

Published on: August 12, 2013

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Enhanced proton conductivity in a layered coordination polymer.

Ricardo F Mendes1, Paula Barbosa2, Eddy M Domingues2

  • 1Department of Chemistry , CICECO - Aveiro Institute of Materials , University of Aveiro , 3810-193 Aveiro , Portugal .

Chemical Science
|September 3, 2020
PubMed
Summary

A novel gadolinium coordination polymer exhibits significantly enhanced proton conductivity upon structural transformation. This transformation, driven by heat and humidity, is key to achieving high proton conduction in these materials.

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Area of Science:

  • Materials Science
  • Solid-State Chemistry
  • Coordination Chemistry

Background:

  • Proton conductivity in coordination polymers is crucial for energy applications.
  • Layered materials offer potential for ion transport.
  • Understanding structural transformations is key to optimizing conductivity.

Purpose of the Study:

  • To investigate the proton conductivity of a gadolinium-based coordination polymer.
  • To explore the relationship between structural transformation and proton conductivity.
  • To identify factors enabling high proton conduction.

Main Methods:

  • Synthesis and characterization of [Gd(H4nmp)(H2O)2]Cl·2H2O (1).
  • In-situ monitoring of structural changes under varying temperature and humidity.
  • Measurement of proton conductivity at different conditions.

Main Results:

  • Compound 1 transforms into compound 2 ([Gd2(H3nmp)2]·xH2O) with increased proton conductivity.
  • Conductivity increases from 1.23 × 10^-5 S cm^-1 (40 °C, 98% RH) to 0.51 S cm^-1 (94 °C, 98% RH) upon transformation.
  • As-synthesized 2 shows high conductivity (3.79 × 10^-2 S cm^-1 at 94 °C, 98% RH).

Conclusions:

  • Dynamic structural transformation with water insertion and chloride release is critical for high proton conduction.
  • The material demonstrates potential as a proton conductor under humid conditions.
  • Further research into similar dynamic transformations could yield advanced proton-conducting materials.