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Related Concept Videos

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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UV–Vis Spectroscopy: Molecular Electronic Transitions01:16

UV–Vis Spectroscopy: Molecular Electronic Transitions

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In Ultraviolet–Visible (UV–Vis) spectroscopy, the absorption of electromagnetic radiation is used to probe the electronic structure of molecules. This technique provides insights into molecular electronic transitions, particularly the movement of electrons between different molecular orbitals. Radiation is absorbed if the energy of the electromagnetic radiation passing through the molecule is precisely equal to the energy difference between the excited and ground states. During this...
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Colors and Magnetism03:02

Colors and Magnetism

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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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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

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The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
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Introduction to Mechanisms of Enzyme Catalysis01:13

Introduction to Mechanisms of Enzyme Catalysis

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For many years, scientists thought that enzyme-substrate binding took place in a simple "lock-and-key" fashion. This model stated that the enzyme and substrate fit together perfectly in one instantaneous step. However, current research supports a more refined view scientists call induced fit. The induced-fit model expands upon the lock-and-key model by describing a more dynamic interaction between enzyme and substrate. As the enzyme and substrate come together, their interaction causes...
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Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

2.0K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
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Updated: Oct 17, 2025

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Visible Light-Induced Transition Metal Catalysis.

Kelvin Pak Shing Cheung1, Sumon Sarkar1, Vladimir Gevorgyan1

  • 1Department of Chemistry and Biochemistry, The University of Texas at Dallas, Richardson, Texas 75080, United States.

Chemical Reviews
|October 8, 2021
PubMed
Summary
This summary is machine-generated.

Visible light transition metal catalysis offers a novel approach to organic photocatalysis. This method uses a single transition metal complex for both light harvesting and catalysis, improving reactions and enabling new transformations.

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Area of Science:

  • Organic chemistry
  • Photocatalysis
  • Transition metal catalysis

Background:

  • Visible light photocatalysis is a rapidly advancing field in organic chemistry.
  • Transition metal complexes are increasingly used as photocatalysts.
  • Conventional photoredox chemistry often employs dual photocatalysis with exogenous photosensitizers.

Purpose of the Study:

  • To review the early development and recent advances in visible light-induced transition metal catalysis.
  • To highlight the unique advantages of this approach compared to conventional methods.

Main Methods:

  • Review of existing literature on visible light-induced transition metal catalysis.
  • Analysis of the mechanisms and applications of this catalytic system.

Main Results:

  • Visible light transition metal catalysis enables unprecedented organic transformations.
  • This approach improves known organic reactions through synergistic catalyst-substrate interactions and photoinduced processes.
  • A single transition metal complex performs both light harvesting and catalytic functions, simplifying the catalytic cycle.

Conclusions:

  • Visible light-induced transition metal catalysis represents a significant paradigm shift in organic photocatalysis.
  • This field holds great promise for the development of novel synthetic methodologies.