Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Colors and Magnetism03:02

Colors and Magnetism

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 eye.
Formation of Complex Ions03:45

Formation of Complex Ions

A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
Coordination Number and Geometry02:57

Coordination Number and Geometry

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.
Ionic Crystal Structures02:42

Ionic Crystal Structures

Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Valence Bond Theory02:42

Valence Bond Theory

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...

También podría leer

Artículos Relacionados

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

Ordenar por
Same author

Mechanistic insights into radical formation and functionalization in copper/<i>N</i>-fluorobenzenesulfonimide radical-relay reactions.

Chemical science·2024
Same author

Understanding Antiferromagnetic and Ligand Field Effects on Spin Crossover in a Triple-Decker Dimeric Cr(II) Complex.

Journal of the American Chemical Society·2023
Same author

Correction: Radical ring-opening polymerization of sustainably-derived thionoisochromanone.

Chemical science·2023
Same author

Radical ring-opening polymerization of sustainably-derived thionoisochromanone.

Chemical science·2023
Same author

Metal-Carbodithioate-Based 3D Semiconducting Metal-Organic Framework: Porous Optoelectronic Material for Energy Conversion.

ACS applied materials & interfaces·2023
Same author

Thanks for the Memories.

Inorganic chemistry·2022
Same journal

Gas-Responsive Metal-Organic Frameworks for Adaptive Thermal Energy Storage with Tunable Charge-Discharge Temperatures.

Journal of the American Chemical Society·2026
Same journal

Engineering a Thiamine-Dependent Benzoylformate Decarboxylase for Stereodivergent Radical C(sp<sup>3</sup>)-C(sp<sup>3</sup>) Bond Formation.

Journal of the American Chemical Society·2026
Same journal

Accelerated Directional Proton-Coupled Electron Transfer Enabled by Intrinsic Dipole Field in Biomimetic α-Helical Structure.

Journal of the American Chemical Society·2026
Same journal

Alternating Current-Driven Hydrogen Isotope Labeling of Aliphatic Amines Using 1,3-Propanedithiol as an Efficient Hydrogen Atom Transfer Reagent.

Journal of the American Chemical Society·2026
Same journal

Two-Dimensional van der Waals Polar Metal MoOBr<sub>2</sub>.

Journal of the American Chemical Society·2026
Same journal

Negatively Curved Chiral Bilayer Nanographene.

Journal of the American Chemical Society·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: Jun 7, 2026

Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides
11:04

Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides

Published on: September 7, 2019

Un complejo de superóxido aniónico, tetragonal de cobre (II) superóxido.

Patrick J Donoghue1, Aalo K Gupta, David W Boyce

  • 1Department of Chemistry, Supercomputing Institute, and Center for Metals in Biocatalysis, University of Minnesota, 207 Pleasant Street SE, Minneapolis, Minnesota 55455, USA.

Journal of the American Chemical Society
|October 28, 2010
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores identificaron un nuevo complejo de cobre (II) superóxido. Este complejo, que presenta un ligando piridinedicarboxamida obstaculizado, exhibe propiedades básicas únicas en las reacciones, ofreciendo nuevos conocimientos sobre los intermediarios de la catálisis de oxidación.

Más Videos Relacionados

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
09:12

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

Published on: May 21, 2019

Videos de Experimentos Relacionados

Last Updated: Jun 7, 2026

Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides
11:04

Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides

Published on: September 7, 2019

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
09:12

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

Published on: May 21, 2019

Área de la Ciencia:

  • Química bioorgánica Química bioorgánica.
  • Coordinación Química de la Coordinación
  • La catálisis por catálisis.

Sus antecedentes:

  • Las especies de cobre-oxígeno son intermediarios cruciales en varias reacciones de catálisis de oxidación.
  • Comprender la estructura y la reactividad de estos intermediarios es clave para diseñar catalizadores eficientes.
  • Estudios anteriores han explorado los complejos de superóxido de cobre, pero sus funciones y comportamientos precisos siguen siendo áreas de investigación activa.

Objetivo del estudio:

  • Identificar y caracterizar un nuevo complejo de cobre (II) superóxido.
  • Para aclarar las propiedades estructurales y electrónicas de este complejo.
  • Para investigar su reactividad, particularmente en comparación con las especies conocidas de superóxido de cobre.

Principales métodos:

  • Síntesis de un complejo de superóxido de cobre (II) apoyado por un ligando de piridinedicarboxamida estéricamente inhibido.
  • Caracterización espectroscópica utilizando UV-vis, RMN, EPR y espectroscopia Raman de resonancia.
  • Cálculos de la Teoría Funcional de Densidad (DFT) para proponer la estructura del complejo.
  • Estudios de reactividad que involucran la reacción con un precursor de cobre (I) y fenoles.

Principales resultados:

  • Identificación de un complejo estable de superóxido de Cu (II) con una estructura tetragonal de superóxido de extremo propuesto.
  • Los datos espectroscópicos (UV-vis, RMN, EPR, resonancia Raman) y los cálculos DFT apoyan la estructura propuesta.
  • El complejo reacciona con [{tmpa}Cu{CH3CN}]OTf para formar una especie trans-1,2-peroxodicopro{II}.
  • En las reacciones con los fenoles, el complejo funciona como una base, a diferencia de otros conocidos Cu (II) - superóxido complejos que actúan como electrófilos.

Conclusiones:

  • Se ha sintetizado y caracterizado con éxito un nuevo complejo Cu(II) -superoxido.
  • Los hallazgos proporcionan información valiosa sobre la naturaleza de los intermediarios de cobre y oxígeno en la catálisis de oxidación.
  • La reactividad básica única de este complejo abre nuevas vías para aplicaciones catalíticas y estudios mecanicistas.