Jove
Visualize
Contact Us

Related Concept Videos

Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

1.6K
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...
1.6K
EDTA: Chemistry and Properties01:22

EDTA: Chemistry and Properties

3.9K
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...
3.9K
Complexometric Titration: Ligands00:43

Complexometric Titration: Ligands

2.6K
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...
2.6K
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

25.6K
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...
25.6K
Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

972
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...
972
Extraction: Advanced Methods00:56

Extraction: Advanced Methods

1.3K
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...
1.3K

You might also read

Related Articles

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

Sort by
Same author

Cationic Group 13/14/15 Element Chain Compounds with Pnictogen-Donor Ligands.

Inorganic chemistry·2026
Same author

Selective white phosphorus activation and functionalization with inorganic Grignard reagents.

Chemical science·2026
Same author

A route to asymmetrically substituted secondary phosphines.

Chemical communications (Cambridge, England)·2026
Same author

Inorganic Cobalt Sandwich Complex [(η<sup>5</sup>-P<sub>5</sub>)Co(η<sup>3</sup>-P<sub>3</sub>)]<sup></sup>.

Journal of the American Chemical Society·2026
Same author

Synthesis of Cobalt-Centered Inorganic Sandwich Complexes.

Journal of the American Chemical Society·2026
Same author

Taming of Low-Valent Arsenic Compounds and Transfer of Nascent As<sub>2</sub> Facilitated by a Frustrated Lewis Pair.

Angewandte Chemie (International ed. in English)·2025
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 Experiment Video

Updated: Apr 4, 2026

Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase
06:31

Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase

Published on: March 19, 2020

7.8K

E4 Butterfly Complexes (E=P, As) as Chelating Ligands.

Christoph Schwarzmaier1, Sebastian Heinl1, Gábor Balázs1

  • 1Institut für Anorganische Chemie der Universität Regensburg, 93040 Regensburg (Germany).

Angewandte Chemie (International Ed. in English)
|September 3, 2015
PubMed
Summary
This summary is machine-generated.

New bidentate phosphane and arsane ligands with narrow bite angles were synthesized. These ligands react with copper salts to form novel spiro and monoadduct compounds, expanding coordination chemistry.

Keywords:
arsenicbutterfly complexeschelate ligandsphosphorusprotonation

More Related Videos

A Study of the Complexation of MercuryII with Dicysteinyl Tetrapeptides by Electrospray Ionization Mass Spectrometry
12:59

A Study of the Complexation of MercuryII with Dicysteinyl Tetrapeptides by Electrospray Ionization Mass Spectrometry

Published on: January 8, 2016

8.5K
Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
19:58

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions

Published on: July 30, 2017

10.4K

Related Experiment Videos

Last Updated: Apr 4, 2026

Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase
06:31

Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase

Published on: March 19, 2020

7.8K
A Study of the Complexation of MercuryII with Dicysteinyl Tetrapeptides by Electrospray Ionization Mass Spectrometry
12:59

A Study of the Complexation of MercuryII with Dicysteinyl Tetrapeptides by Electrospray Ionization Mass Spectrometry

Published on: January 8, 2016

8.5K
Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
19:58

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions

Published on: July 30, 2017

10.4K

Area of Science:

  • Organometallic Chemistry
  • Coordination Chemistry

Background:

  • Bidentate phosphane and arsane ligands are crucial in coordination chemistry.
  • Exploring ligands with narrow bite angles can lead to unique coordination geometries.

Purpose of the Study:

  • To report the coordination properties of new bidentate phosphane and arsane ligands.
  • To investigate the reactions of these ligands with copper salts.
  • To characterize the resulting coordination compounds.

Main Methods:

  • Synthesis of novel phosphane and arsane ligands.
  • Reactions with copper salts ([Cu(CH3CN)4][BF4]).
  • Characterization using spectroscopic methods (NMR, IR) and single-crystal X-ray diffraction.
  • Density Functional Theory (DFT) calculations for protonation studies.

Main Results:

  • Formation of a spiro compound [{{Cp'''Fe(CO)2}2(μ3,η(1:1:1:1)-P4)}2Cu](+)[BF4](-) (2) and a monoadduct [{Cp'''Fe(CO)2}2(μ3,η(1:1:2)-P4){Cu(MeCN)}](+)[BF4](-) (3) from phosphane ligand 1a.
  • Formation of a spiro compound [{{Cp'''Fe(CO)2}2(μ3,η(1:1:1:1)-As4)}2Cu](+)[BF4](-) (5) from arsane ligand 1b.
  • Protonation of ligand 1a occurs at the 'wing tip' phosphorus atoms, consistent with DFT calculations.

Conclusions:

  • New bidentate phosphane and arsane ligands exhibit interesting coordination behavior with copper.
  • The narrow bite angle of these ligands facilitates the formation of complex structures like spiro compounds.
  • Spectroscopic and crystallographic data confirm the structures and bonding in the novel complexes.