Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

8.7K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
8.7K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation02:47

Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation

18.7K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
18.7K
Nuclear Transmutation03:20

Nuclear Transmutation

17.9K
Nuclear transmutation is the conversion of one nuclide into another. It can occur by the radioactive decay of a nucleus, or the reaction of a nucleus with another particle. The first manmade nucleus was produced in Ernest Rutherford’s laboratory in 1919 by a transmutation reaction, the bombardment of one type of nuclei with other nuclei or with neutrons. Rutherford bombarded nitrogen-14 atoms with high-speed α particles from a natural radioactive isotope of radium and observed...
17.9K
Regioselectivity and Stereochemistry of Hydroboration02:36

Regioselectivity and Stereochemistry of Hydroboration

8.3K
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...
8.3K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

1.9K
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...
1.9K
Nuclear Stability03:18

Nuclear Stability

19.4K
Protons and neutrons, collectively called nucleons, are packed together tightly in a nucleus. With a radius of about 10−15 meters, a nucleus is quite small compared to the radius of the entire atom, which is about 10−10 meters. Nuclei are extremely dense compared to bulk matter, averaging 1.8 × 1014 grams per cubic centimeter. If the earth’s density were equal to the average nuclear density, the earth’s radius would be only about 200 meters.
To hold positively charged protons together...
19.4K

También podría leer

Artículos Relacionados

Artículos vinculados a este trabajo por autores compartidos, revista y gráfico de citas.

Ordenar por
Same author

Dissecting Reaction Paths with the Independent Gradient Model: The Case of a Key Reductive Elimination Step at Cobalt(IV).

The journal of physical chemistry. A·2026
Same author

Monocarborane-stabilized iodonium salts enable regioselective B12-iodination of [CB<sub>11</sub>H<sub>12</sub>]<sup></sup>.

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

Obtaining single crystals containing cationic porphyrins from aqueous solutions: a systematic approach including nano-crystallization, organic modifiers and gel crystallization.

IUCrJ·2025
Same author

Dissecting reactions with the independent gradient model: the case of the stereoselective insertion of a Fischer-type carbene ligand into a Mn-C bond.

Physical chemistry chemical physics : PCCP·2025
Same author

Microwave-assisted Pd-catalyzed B-N cross-coupling for efficient functionalization of the carbaborate [CB<sub>11</sub>H<sub>12</sub>]<sup></sup>.

Chemical communications (Cambridge, England)·2025
Same author

Synergistic effects of combining phototherapeutics with traditional treatment modalities in oncology.

Chemical communications (Cambridge, England)·2025
JoVE
x logofacebook logolinkedin logoyoutube logo
ACERCA DE JoVE
Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
AUTORES
Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
BIBLIOTECARIOS
TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
INVESTIGACIÓN
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
EDUCACIÓN
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
Términos y Condiciones de Uso
Política de Privacidad
Políticas

Video Experimental Relacionado

Updated: Aug 27, 2025

Photochemical Oxidative Growth of Iridium Oxide Nanoparticles on CdSe@CdS Nanorods
05:41

Photochemical Oxidative Growth of Iridium Oxide Nanoparticles on CdSe@CdS Nanorods

Published on: February 11, 2016

9.6K

Un intermediario de borenio estabilizado con iridio

Mustapha Hamdaoui1, Fan Liu1, Yann Cornaton2

  • 1Department of Chemistry, Zheijang University, Hangzhou 310027, China.

Journal of the American Chemical Society
|September 29, 2022
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores descubrieron un nuevo complejo de clúster de boro de iridio que activa el hidroboraneo, formando un ion de boro único. Este hallazgo revela una interacción inusual e inicia un nuevo mecanismo de "caminata en jaula" en la superficie del cúmulo de boro.

Más Videos Relacionados

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
09:45

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene

Published on: March 20, 2017

10.5K
IridiumIII Luminescent Probe for Detection of the Malarial Protein Biomarker Histidine Rich Protein-II
12:52

IridiumIII Luminescent Probe for Detection of the Malarial Protein Biomarker Histidine Rich Protein-II

Published on: July 7, 2015

9.3K

Videos de Experimentos Relacionados

Last Updated: Aug 27, 2025

Photochemical Oxidative Growth of Iridium Oxide Nanoparticles on CdSe@CdS Nanorods
05:41

Photochemical Oxidative Growth of Iridium Oxide Nanoparticles on CdSe@CdS Nanorods

Published on: February 11, 2016

9.6K
Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
09:45

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene

Published on: March 20, 2017

10.5K
IridiumIII Luminescent Probe for Detection of the Malarial Protein Biomarker Histidine Rich Protein-II
12:52

IridiumIII Luminescent Probe for Detection of the Malarial Protein Biomarker Histidine Rich Protein-II

Published on: July 7, 2015

9.3K

Área de la Ciencia:

  • Química organometálica
  • Química de los racimos de boro
  • Química inorgánica

Sus antecedentes:

  • Los grupos poliédricos de boro son la clave para estabilizar las especies reactivas.
  • Los sistemas organometálicos ofrecen soluciones para problemas químicos desafiantes como la activación de enlaces E-H.

Objetivo del estudio:

  • Para explorar nuevos sistemas organometálicos basados en grupos de boro poliédricos.
  • Investigar la activación B-H del hidroborano por un complejo de clúster de iridio y boro.
  • Caracterizar el nuevo catión de boro (borenio) resultante y sus interacciones.

Principales métodos:

  • Reacción de activación de B-H fácil y limpia.
  • Caracterización de nuevos compuestos mediante espectroscopia RMN y análisis elemental.
  • Difracción de rayos X de cristal único y espectroscopia de fotoelectrones de rayos X para compuestos clave.
  • Métodos teóricos para elucidar los mecanismos de reacción.

Principales resultados:

  • Se sintetizó un nuevo complejo de clúster de boro de iridio y reaccionó con hidroborano.
  • Se formó un catión de boro estabilizado por metales de transición sin precedentes.
  • Se observó una interacción intramolecular B·H inusual, propuesta como una inserción detenida.
  • Pruebas de iridio "caminando en jaula" alrededor del grupo de boro, apoyado por el intercambio H-D.

Conclusiones:

  • El estudio informa de un nuevo intermedio de borenio estabilizado por un grupo de boro de iridio.
  • Se identifica una interacción B··H intramolecular como una característica clave y un paso inicial para el "caminar en jaula".
  • Los hallazgos avanzan en la comprensión de la reactividad y los mecanismos en la química de clúster de boro y la catálisis organometálica.