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Related Concept Videos

Valence Bond Theory02:42

Valence Bond Theory

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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...
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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...
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Properties of Organometallic Compounds01:23

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Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
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Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

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In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
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Properties of Transition Metals02:58

Properties of Transition Metals

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Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
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Crystal Field Theory - Octahedral Complexes02:58

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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...
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Reverse Microemulsion-mediated Synthesis of Monometallic and Bimetallic Early Transition Metal Carbide and Nitride Nanoparticles
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Transition Metal Carbide Complexes.

Anders Reinholdt1, Jesper Bendix1

  • 1Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen, Denmark.

Chemical Reviews
|November 19, 2021
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Summary
This summary is machine-generated.

Carbide complexes are rare due to limited synthetic methods. This review details strategies for synthesizing and understanding the reactivity and electronic structure of these unique carbon-metal compounds.

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Area of Science:

  • Organometallic Chemistry
  • Inorganic Chemistry

Background:

  • Carbide complexes, compounds featuring a metal-carbon bond with a formal negative charge on carbon, are a rare but important class of molecules.
  • Their scarcity stems from the limited scope of synthetic methodologies rather than inherent instability.

Purpose of the Study:

  • To provide a comprehensive overview of synthetic strategies for generating terminal, bridging, and cluster carbide complexes.
  • To survey the diverse reactivity of carbide ligands, including their role as C1 synthons, in cross-coupling, and in Fischer-Tropsch-type reactions.
  • To discuss the application of carbide complexes in catalysis and examine their spectroscopic characteristics for structural and electronic elucidation.

Main Methods:

  • Review of established and emerging synthetic routes for carbide complex formation.
  • Analysis of stoichiometric and catalytic reactions involving carbide complexes.
  • Examination of spectroscopic techniques (e.g., NMR, IR, X-ray crystallography) for characterizing carbide complexes.

Main Results:

  • Detailed synthetic pathways are presented for various types of carbide complexes.
  • Carbide ligands exhibit versatile reactivity, acting as nucleophiles and participating in bond-forming reactions.
  • Spectroscopic data provide insights into the electronic structure and bonding of carbide functionalities.

Conclusions:

  • This review consolidates knowledge on carbide complex synthesis and reactivity, highlighting their potential in catalysis.
  • Understanding synthetic limitations and reactivity patterns is crucial for expanding the utility of these organometallic compounds.