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 Experiment Videos

Halide effects in transition metal catalysis.

Keith Fagnou1, Mark Lautens

  • 1Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, M5S 3H6 Canada.

Angewandte Chemie (International Ed. in English)
|December 20, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Synthesis of Iodinated Semisaturated Heterobicycles via a Temporal Dual Metal-Catalyzed Cycloaddition/Photochemical Carbohalogenation.

Journal of the American Chemical Society·2026
Same author

Strategies Toward Accessing Enantioenriched (Hetero)Benzo-Fused 5- and 6- Membered Rings via Intermolecular Carbometalation.

Angewandte Chemie (International ed. in English)·2026
Same author

Development of a Dual Chemical Probe for the USP16 and HDAC6 Zinc-Finger Ubiquitin-Binding Domain.

Journal of medicinal chemistry·2026
Same author

Synthesis of Spiroindenes via Palladium Catalysis Using Oxabicycles as Acetylene Surrogates.

Organic letters·2025
Same author

Asymmetric Allylboration of α-Alkoxy-enones: Access to Enantioenriched Tertiary α-Hydroxy Ketones.

Organic letters·2025
Same author

Photoexcited Transition-Metal Catalyzed Carbon-Halogen Bond Formation.

Angewandte Chemie (International ed. in English)·2025

Halide ligands on transition metal catalysts significantly tune reactivity and selectivity. Manipulating these ligands offers a powerful strategy for developing new catalytic systems with predictable outcomes.

Area of Science:

  • Catalysis
  • Organometallic Chemistry
  • Inorganic Chemistry

Background:

  • Halide ions are common ligands in transition metal catalysts, with most commercial catalysts being halo-metal complexes.
  • The metal-halide functionality is increasingly recognized as a key element for tuning catalyst reactivity and selectivity.

Purpose of the Study:

  • To review the physical properties of halide ligands.
  • To discuss their effects on stoichiometric and catalytic transition metal processes.
  • To highlight the potential of the metal-halide moiety as a tunable feature in catalyst development.

Main Methods:

  • Review of existing literature on transition metal catalysis involving halide ligands.
  • Analysis of steric and electronic properties of various halide ligands.

Related Experiment Videos

  • Examination of trends in reactivity and enantioselectivity influenced by halide variations.
  • Main Results:

    • Variation of halide ligands predictably alters catalyst reactivity and selectivity without rendering the system unreactive.
    • Halide ligands, often overlooked, significantly impact enantioselectivity in asymmetric catalysis.
    • Intriguing and synthetically useful trends in metal-halide catalysis are apparent, though mechanisms are not always fully understood.

    Conclusions:

    • The metal-halide moiety is a crucial, tunable functionality in transition metal catalysis.
    • Strategic manipulation of halide ligands can lead to the development of novel and improved catalytic systems.
    • Further investigation into halide ligand effects can unlock new possibilities in asymmetric synthesis.