Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Complexometric Titration: Ligands00:43

Complexometric Titration: Ligands

Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

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...
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction01:16

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

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...
EDTA: Chemistry and Properties01:22

EDTA: Chemistry and Properties

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...
Valence Bond Theory02:42

Valence Bond Theory

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...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Novel 4,8-benzobisthiazole copolymers and their field-effect transistor and photovoltaic applications.

Journal of materials chemistry. C·2026
Same author

Dual-Action NSAID-Gold(I) Alkynyl Hybrids for Synergistic Anti-Inflammatory and Anticancer Therapy of Colorectal Cancer.

Inorganic chemistry·2026
Same author

Silver-selenium hybrid nanocomposite with combined cytotoxic and metabolic reprogramming effects in triple-negative breast cancer.

Colloids and surfaces. B, Biointerfaces·2026
Same author

A third-generation rhodium-based nanophotosensitizer for precision photodynamic cancer therapy.

Journal of colloid and interface science·2026
Same author

Accelerating Neodymium's First-Shell Dynamics toward Improved Metal Recovery.

The journal of physical chemistry. B·2025
Same author

A Wearable and Highly Sensitive PVDF-TrFE-BaTiO<sub>3</sub> Piezoelectric Sensor for Wireless Monitoring of Arterial Signal.

ACS applied electronic materials·2025

Related Experiment Video

Updated: Jul 4, 2026

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
12:30

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework

Published on: April 9, 2018

Novel dithiolene complexes incorporating conjugated electroactive ligands.

Peter J Skabara1, Cristina Pozo-Gonzalo, Nora Lardiés Miazza

  • 1WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, UK G1 1XL. peter.skabara@strath.ac.uk

Dalton Transactions (Cambridge, England : 2003)
|June 4, 2008
PubMed
Summary

New metal dithiolene complexes with thiophene units were synthesized and electrochemically studied. These materials exhibit tunable redox properties and form stable polymer films, showing potential as charge transfer materials.

More Related Videos

Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase
06:31

Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase

Published on: March 19, 2020

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
11:44

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds

Published on: October 18, 2018

Related Experiment Videos

Last Updated: Jul 4, 2026

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
12:30

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework

Published on: April 9, 2018

Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase
06:31

Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase

Published on: March 19, 2020

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
11:44

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds

Published on: October 18, 2018

Area of Science:

  • Coordination Chemistry
  • Materials Science
  • Electrochemistry

Background:

  • Dithiolene complexes are versatile in coordination chemistry.
  • Thiophene-based ligands offer tunable electronic properties.
  • Metal complexes are explored for electronic and charge transfer applications.

Purpose of the Study:

  • Synthesize novel metal dithiolene complexes with terthiophene and bis(para-methoxyphenyl)thiophene ligands.
  • Characterize the electrochemical and optical properties of these new complexes.
  • Investigate the potential of these complexes in forming conductive polymer films and charge transfer materials.

Main Methods:

  • Synthesis of metal dithiolene complexes (Ni, Pd, Au).
  • Electrochemical characterization using cyclic voltammetry.
  • UV-vis spectroelectrochemistry for optical property analysis.
  • Electrochemical polymerization of terthiophene derivatives.
  • Isolation and conductivity measurements of charge transfer materials.

Main Results:

  • Successful synthesis of Ni, Pd, and Au dithiolene complexes with yields ranging from 38-99%.
  • Nickel complexes showed low oxidation potentials (-0.12 to -0.25 V vs Ag/AgCl) due to electron-rich dithiolene centers.
  • All synthesized complexes exhibited ligand-based redox activity.
  • Electrochemical polymerization of terthiophene derivatives yielded stable films with broad absorption.
  • Charge transfer materials derived from specific complexes showed conductivities between 9 x 10(-6) and 7 x 10(-8) S cm(-1).

Conclusions:

  • The synthesized metal dithiolene complexes possess tunable electrochemical properties.
  • Electrochemical polymerization leads to stable, broadly absorbing films.
  • The materials show promise for applications in charge transfer and conductive materials.