Jove
Visualize
Contact Us

Related Concept Videos

Extraction: Advanced Methods00:56

Extraction: Advanced Methods

526
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...
526
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

651
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...
651
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

21.5K
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...
21.5K
Colors and Magnetism03:02

Colors and Magnetism

12.3K
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...
12.3K
Valence Bond Theory02:42

Valence Bond Theory

9.2K
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...
9.2K
Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

470
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...
470

You might also read

Related Articles

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

Sort by
Same author

Hydrophobic pocket engineering of arylmalonate decarboxylase expands its substrate scope towards the synthesis of the (<i>R</i>)-enantiomers of sterically hindered carboxylic acids.

Chemical communications (Cambridge, England)·2026
Same author

Oxovanadium-Catalyzed Epoxidation of Methyl Oleate: Ligand Effects.

ACS omega·2026
Same author

Metalloid Tin Clusters, Sn<sub><i>n</i></sub><i>t</i>Bu<sub>m</sub>, with α-Sn-Like Structural Motifs.

Inorganic chemistry·2026
Same author

Bis-α,ω-bisacylphosphane oxides: simple access to crosslinked polymers with tunable properties.

Journal of materials chemistry. A·2026
Same author

Isomorphism in a Series of Five Homologous Compounds.

Crystal growth & design·2026
Same author

Silylated Stannanes and Stannides.

Inorganic chemistry·2026
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: Sep 9, 2025

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
10:51

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Published on: April 10, 2015

12.2K

Synthesis and Characterization of Phosphanophenolate-Based Rare-Earth Metal-Copper Complexes.

Andreas Fleißner1, Viktoria Rehbein1, Alexandra Haidinger1

  • 1Institute of Inorganic Chemistry, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria.

Inorganic Chemistry
|August 28, 2025
PubMed
Summary

This study synthesizes novel dinuclear rare-earth metal(III)-copper(I) complexes using a phosphine-phenolate ligand. An alternative route proved less effective, but triflate exchange reactions yielded new tert-butoxide complexes.

More Related Videos

[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
09:12

[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

Published on: May 21, 2019

9.4K
Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
07:14

Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers

Published on: May 12, 2023

3.1K

Related Experiment Videos

Last Updated: Sep 9, 2025

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
10:51

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Published on: April 10, 2015

12.2K
[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
09:12

[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

Published on: May 21, 2019

9.4K
Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
07:14

Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers

Published on: May 12, 2023

3.1K

Area of Science:

  • Organometallic Chemistry
  • Coordination Chemistry
  • Rare-Earth Metal Complexes

Background:

  • Rare-earth metal complexes with phosphine-phenolate ligands are of interest for their unique electronic and structural properties.
  • Developing efficient synthetic routes to heterobimetallic complexes is crucial for exploring new materials and catalytic applications.

Purpose of the Study:

  • To synthesize and characterize novel dinuclear rare-earth metal(III)-copper(I) complexes.
  • To explore alternative synthetic strategies for heterobimetallic rare-earth metal-copper complexes.
  • To investigate ligand exchange reactions on pre-formed dinuclear complexes.

Main Methods:

  • Synthesis of dinuclear rare-earth metal(III)-copper(I) complexes via reaction of [LnIII(OArP-κ2O,P)3] with copper(I) triflate.
  • Attempted synthesis of heterobimetallic complexes from a mononuclear copper complex and rare-earth metal amides.
  • Triflate exchange reactions on dinuclear complexes using various nucleophiles, including alkaline metal amides, alkyls, and alkoxides.
  • Characterization using NMR, UV-vis, IR spectroscopy, single-crystal X-ray diffraction, and elemental analysis.
  • Magnetic moment determination using the Evans NMR method.

Main Results:

  • Clean synthesis of dinuclear rare-earth metal(III)-copper(I) complexes [LnIII(OTf)(μ-OArP-1κ1O,2κ1P)3CuI] (2-Ln) was achieved.
  • An alternative synthetic route starting from a mononuclear copper complex yielded heterobimetallic complexes in low yields with side-products.
  • Triflate exchange was successful only with potassium tert-butoxide (KOtBu), yielding [LnIII(OtBu)(μ-OArP-1κ1O,2κ1P)3CuI] (4-Ln).
  • Structural and spectroscopic data confirmed the formation and characterization of the new complexes.

Conclusions:

  • The direct reaction of rare-earth metal complexes with copper(I) triflate is an efficient method for synthesizing dinuclear complexes.
  • The explored alternative synthetic route is less favorable for generating heterobimetallic rare-earth metal-copper complexes.
  • The tert-butoxide complexes (4-Ln) represent a new class of heterobimetallic compounds accessible via triflate exchange.