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

Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

4.9K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
4.9K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

1.8K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.8K
Preparation and Reactions of Thiols02:33

Preparation and Reactions of Thiols

6.3K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
6.3K
Electrophilic Aromatic Substitution: Sulfonation of Benzene01:22

Electrophilic Aromatic Substitution: Sulfonation of Benzene

6.1K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
6.1K
Regioselectivity and Stereochemistry of Hydroboration02:36

Regioselectivity and Stereochemistry of Hydroboration

8.2K
A significant aspect of hydroboration–oxidation is the regio- and stereochemical outcome of the reaction.
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
8.2K
Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

47.3K
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
47.3K

You might also read

Related Articles

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

Sort by
Same author

Cyclometallation across metal-carbon bonds; <i>exo</i>-metallated metallacyclopentadiene synthesis.

Dalton transactions (Cambridge, England : 2003)·2026
Same author

Two approaches to phosphaniminocarbyne complexes.

Dalton transactions (Cambridge, England : 2003)·2026
Same author

Pnictogen-functionalised isocyanide ligands.

Dalton transactions (Cambridge, England : 2003)·2025
Same author

Alkynyltellurolato ligands including a solvatochromic rhenium(I) complex.

Chemical communications (Cambridge, England)·2025
Same author

The Interplay of Methylidyne and Carbido Species: Modeling a Fundamental Step in the Fischer-Tropsch Synthesis.

Angewandte Chemie (International ed. in English)·2025
Same author

Electrophilic As-functionalisation of σ-arsolido complexes.

Dalton transactions (Cambridge, England : 2003)·2024
Same journal

Cation-templated synthesis of a Fe<sub>4</sub>Co<sub>20</sub> cyanometallate cluster.

Dalton transactions (Cambridge, England : 2003)·2026
Same journal

High-field multinuclear MAS NMR and synchrotron XANES reveal the influence of strontium salt chemistry on geopolymer nanostructure.

Dalton transactions (Cambridge, England : 2003)·2026
Same journal

Carbonyl insertion into metal-boron based clusters: pathway to a rhodathiacarborane.

Dalton transactions (Cambridge, England : 2003)·2026
Same journal

Simulation of displacement damage in CsPbBr<sub>3</sub> induced by neutron irradiation based on the Monte Carlo method.

Dalton transactions (Cambridge, England : 2003)·2026
Same journal

Photocatalysis-tribocatalysis synergy in oxygen vacancy-rich Zn<sub>2</sub>SnO<sub>4</sub>: mechanism and enhanced all-day performance.

Dalton transactions (Cambridge, England : 2003)·2026
Same journal

Two-dimensional Co/Ni coordination polymers: structure-activity relationship and bifunctional performance for electrocatalysis and energy storage.

Dalton transactions (Cambridge, England : 2003)·2026
See all related articles

Related Experiment Video

Updated: Jul 17, 2025

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
07:07

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology

Published on: March 12, 2015

9.7K

Free and coordinated biarsolyls.

Ryan M Kirk1, Anthony F Hill1

  • 1Research School of Chemistry, Australian National University, Canberra, ACT, Australia. a.hill@anu.edu.au.

Dalton Transactions (Cambridge, England : 2003)
|September 4, 2023
PubMed
Summary
This summary is machine-generated.

Researchers identified a novel biarsolyl complex, a significant advancement in organometallic chemistry. This discovery provides new insights into arsenic-containing compounds and their synthesis.

More Related Videos

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
08:47

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates

Published on: March 6, 2019

9.5K
Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
08:56

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions

Published on: November 30, 2022

2.8K

Related Experiment Videos

Last Updated: Jul 17, 2025

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
07:07

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology

Published on: March 12, 2015

9.7K
Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
08:47

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates

Published on: March 6, 2019

9.5K
Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
08:56

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions

Published on: November 30, 2022

2.8K

Area of Science:

  • Organometallic Chemistry
  • Coordination Chemistry
  • Main Group Chemistry

Background:

  • Organoarsenic compounds are versatile ligands in coordination chemistry.
  • Biarsolyl ligands offer unique electronic and steric properties.
  • Synthesis of novel organometallic complexes is crucial for materials science.

Purpose of the Study:

  • To synthesize and characterize a novel biarsolyl complex.
  • To investigate the structural and electronic properties of the new complex.
  • To explore the reactivity of biarsolyl ligands in organometallic synthesis.

Main Methods:

  • Strategic synthesis of the biarsolyl complex.
  • X-ray crystallography for structural determination.
  • Density functional theory (DFT) calculations for electronic structure analysis.

Main Results:

  • Identification of the biarsolyl complex [Mn2{μ-(AsC4Me4)2}(CO)4(C5H4Me)2] as a trace side product.
  • Successful strategic synthesis of the complex from a manganese precursor and a pre-formed biarsolyl ligand.
  • Detailed crystallographic and computational data for the novel complex and free biarsolyls.

Conclusions:

  • The study reports the first structurally characterized biarsolyl complex.
  • The findings provide valuable insights into the coordination chemistry of biarsolyl ligands.
  • This work opens avenues for the development of new arsenic-containing organometallic compounds.