Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Exceptions to the Octet Rule02:55

Exceptions to the Octet Rule

38.0K
Many covalent molecules have central atoms that do not have eight electrons in their Lewis structures. These molecules fall into three categories:
38.0K
Chirality at Nitrogen, Phosphorus, and Sulfur02:30

Chirality at Nitrogen, Phosphorus, and Sulfur

7.1K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
7.1K
VSEPR Theory and the Basic Shapes02:52

VSEPR Theory and the Basic Shapes

85.8K
Overview of VSEPR Theory
85.8K
Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

5.9K
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.
5.9K
VSEPR Theory and the Effect of Lone Pairs04:01

VSEPR Theory and the Effect of Lone Pairs

53.4K
Effect of Lone Pairs of Electrons on Molecule Geometry
53.4K
Coordination Number and Geometry02:57

Coordination Number and Geometry

19.2K
For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
19.2K

También podría leer

Artículos Relacionados

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

Ordenar por
Same author

Ligand rigidity as a design principle for planar pentacoordinate fluorine.

Chemical communications (Cambridge, England)·2026
Same author

SLi<sub>4</sub>X<sub>3</sub><sup>-</sup> (X = Cl, Br, I): fan-shaped superhalogen anions featuring planar tetracoordinate sulfur.

Physical chemistry chemical physics : PCCP·2026
Same author

Cl©K<b><sub>4</sub></b>I<b><sub>4</sub></b><sup>-</sup>: A Star-Like Planar Tetracoordinate Chlorine Superhalogen Anion.

The journal of physical chemistry. A·2026
Same author

Manifestations of Boron-Alkali Metal and Boron-Alkaline-Earth Metal Romances.

Accounts of chemical research·2026
Same author

Planar hexacoordinate chlorine.

Chemical science·2026
Same author

<i>D</i> <sub>2h</sub> HZn<sub>4</sub>S<sub>4</sub><sup>-</sup>: an elongated planar tetracoordinate hydrogen star.

Chemical communications (Cambridge, England)·2025
Same journal

Anharmonic phonons via quantum thermal bath simulations.

The Journal of chemical physics·2026
Same journal

Quantum simulation of alignment dependent differential cross sections in co-propagating molecular beams at cold collision energies.

The Journal of chemical physics·2026
Same journal

Non-additive ion effects on the coil-globule equilibrium of a generic polymer in aqueous salt solutions.

The Journal of chemical physics·2026
Same journal

Insights into the unexpected small reduction of the temperature of maximum density of water by lithium chloride addition.

The Journal of chemical physics·2026
Same journal

Optical frequency comb double-resonance spectroscopy of the 9030-9175 cm-1 states of ethylene.

The Journal of chemical physics·2026
Same journal

Time reversal breaking of colloidal particles in cells.

The Journal of chemical physics·2026
Ver todos los artículos relacionados
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: Feb 20, 2026

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
10:42

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV

Published on: December 29, 2016

11.2K

Planar hexacoordinate sulfur and selenium

Ya-Xuan Cheng1, Li-Xia Bai1, Jin-Chang Guo1

  • 1Institute of Molecular Science, Shanxi University, Taiyuan 030006, China.

The Journal of chemical physics
|February 18, 2026
PubMed
Resumen
Este resumen es generado por máquina.

Researchers predicted the first planar hexacoordinate sulfur and selenium (phS/Se) clusters, X©Li6H62-. These stable structures challenge conventional coordination limits for chalcogens.

Palabras clave:
hexacoordinate sulfurhexacoordinate seleniumplanar clusterscomputational chemistryinorganic chemistrymaterials science

Más Videos Relacionados

Preparation of Large-area Vertical 2D Crystal Hetero-structures Through the Sulfurization of Transition Metal Films for Device Fabrication
08:50

Preparation of Large-area Vertical 2D Crystal Hetero-structures Through the Sulfurization of Transition Metal Films for Device Fabrication

Published on: November 28, 2017

9.6K
Demonstrating the Simplicity and In Situ Temperature Monitoring of the Mechanochemical Synthesis of Metal Chalcogenides Suitable for Thermoelectrics
04:09

Demonstrating the Simplicity and In Situ Temperature Monitoring of the Mechanochemical Synthesis of Metal Chalcogenides Suitable for Thermoelectrics

Published on: August 30, 2024

824

Videos de Experimentos Relacionados

Last Updated: Feb 20, 2026

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
10:42

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV

Published on: December 29, 2016

11.2K
Preparation of Large-area Vertical 2D Crystal Hetero-structures Through the Sulfurization of Transition Metal Films for Device Fabrication
08:50

Preparation of Large-area Vertical 2D Crystal Hetero-structures Through the Sulfurization of Transition Metal Films for Device Fabrication

Published on: November 28, 2017

9.6K
Demonstrating the Simplicity and In Situ Temperature Monitoring of the Mechanochemical Synthesis of Metal Chalcogenides Suitable for Thermoelectrics
04:09

Demonstrating the Simplicity and In Situ Temperature Monitoring of the Mechanochemical Synthesis of Metal Chalcogenides Suitable for Thermoelectrics

Published on: August 30, 2024

824

Área de la Ciencia:

  • Química Computacional
  • Química Inorgánica
  • Ciencia de Materiales

Sus antecedentes:

  • Lograr átomos planares hexacoordinados es un desafío significativo en química.
  • Los elementos calcógenos, como el azufre y el selenio, típicamente exhiben números de coordinación más bajos.

Objetivo del estudio:

  • Predecir y caracterizar nuevos clústeres planares de azufre y selenio hexacoordinados (phS/Se).
  • Investigar la estabilidad estructural y la naturaleza del enlace de estas especies únicas.

Principales métodos:

  • Cálculos de estructura electrónica cuantitativa de alto nivel.
  • Simulaciones de dinámica molecular de Born-Oppenheimer para la evaluación de la estabilidad.
  • Análisis de descomposición de energía-orbitales naturales para valencia química (EDA-NOCV) para el análisis de enlace.

Principales resultados:

  • Se predijeron computacionalmente los primeros clústeres planares de azufre y selenio hexacoordinados, X©Li6H62- (X = S, Se).
  • Estos clústeres adoptan estructuras estables de simetría D6h singlete con un átomo central de S/Se unido a un hexágono de Li, el cual está coronado por átomos de hidrógeno.
  • El análisis de enlace reveló una estructura electrónica única con pares solitarios, enlaces sigma deslocalizados y enlaces iónicos multicéntricos que contribuyen a la estabilidad.

Conclusiones:

  • Los clústeres phS/Se predichos representan un avance, ampliando la química de coordinación de los elementos calcógenos.
  • La alta estabilidad de estas estructuras planares hexacoordinadas se confirmó mediante simulaciones dinámicas.
  • Estos hallazgos abren nuevas vías para la exploración de complejos planares hexacoordinados novedosos en la investigación teórica y experimental.