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The Photochemical Reaction Center01:29

The Photochemical Reaction Center

4.4K
Reaction centers are pigment-protein complexes that initiate energy conversion from photons to chemical entities. Therefore, photochemical reaction center is a more appropriate term that describes these complexes. The Nobel laureates Robert Emerson and William Arnold provided the first experimental evidence of photochemical reaction centers by demonstrating the participation of nearly 2,500 chlorophyll molecules for the release of just one molecule of oxygen. Despite thousands of photosynthetic...
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The Antenna Complex01:15

The Antenna Complex

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Plants and other photosynthetic organisms comprise pigments capable of absorption of direct sunlight. These pigments are present in the reaction center - the main site of photochemical reactions as well as in the antenna complex. Under average light conditions, the rate at which reaction center pigments absorb light is far below the electron transport chain's capacity. As a result, the reaction center alone cannot provide enough energy to drive photosynthesis. The photosynthetic efficiency can...
6.4K
Photosystem I01:27

Photosystem I

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Although structurally similar to photosystem II (PSII), photosystem I (PSI) is has a different electron supplier and electron acceptor.
Both these photosystems work in concert. An excited electron from PSII is relayed to PSI via an electron transport chain in the thylakoid membrane of the chloroplast, which is comprised of the carrier molecule plastoquinone, the dual-protein cytochrome complex, and plastocyanin. As electrons move between PSII and PSI, they lose energy and must be re-energized...
65.6K
Photosystem II01:22

Photosystem II

73.8K
The multi-protein complex photosystem II (PS II) harvests photons and transfers their energy through its bound pigments to its reaction center, and ultimately to photosystem I (PSI) through the electron transport chain. The pigments responsible for caputirng the light energy in photosystems include chlorophyll a, chlorophyll b, and carotenoids.
The pigment molecules are arranged across  two photosystem domains — the antenna complex and the reaction center. The main aim of the pigment...
73.8K
Colors and Magnetism03:02

Colors and Magnetism

12.5K
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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Photoluminescence: Applications01:14

Photoluminescence: Applications

517
Photoluminescence offers a wide range of applications due to its inherent sensitivity and selectivity. This technique allows for both direct and indirect analyses of the analyte. Direct quantitative analysis is possible when the analyte exhibits a favorable quantum yield for fluorescence or phosphorescence. However, an indirect analysis may be feasible if the analyte is not fluorescent or phosphorescent, or if the quantum yield is unfavorable. Indirect methods include reacting the analyte with...
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Related Experiment Video

Updated: Oct 6, 2025

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

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A Photoreactive Iron(II) Complex Luminophore.

Wolfgang Leis1, Miguel A Argüello Cordero2, Stefan Lochbrunner2

  • 1Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, 72076 Tübingen, Germany.

Journal of the American Chemical Society
|January 13, 2022
PubMed
Summary

This study introduces a novel iron(II) complex for light-to-energy conversion. This luminescent chromophore, featuring a triplet metal-to-ligand charge transfer state, demonstrates efficient near-infrared emission and photoreactivity for synthesis.

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Area of Science:

  • Photochemistry
  • Inorganic Chemistry
  • Materials Science

Background:

  • Controlling excited states is key for light-to-energy conversion in molecular systems.
  • Ruthenium complexes are common sensitizers, but alternatives are sought.

Purpose of the Study:

  • To report a novel luminescent and photoreactive iron(II) complex.
  • To investigate its excited state properties and potential applications in light-driven synthesis.

Main Methods:

  • Synthesis of a double cyclometalated iron(II) complex with a phenylphenanthroline framework.
  • Characterization of its photophysical properties, including luminescence decay and excited-state redox potential.
  • Demonstration of its use in a radical cross-coupling reaction.

Main Results:

  • The iron(II) complex populates a triplet metal-to-ligand charge transfer (3MLCT) state as the lowest energy excited state.
  • Near-infrared luminescence was observed with lifetimes of 1-2.4 ns in different phases and 14 ns at 77 K.
  • The complex exhibits a 3MLCT excited-state redox potential of -2 V vs Fc/Fc+.
  • Successful application in the radical cross-coupling of 4-chlorobromobenzene and benzene.

Conclusions:

  • The developed iron(II) complex is a performant sensitizer, analogous to ruthenium complexes.
  • Its favorable excited-state properties, including NIR luminescence and redox potential, enable its use in light-driven synthesis.
  • This work expands the scope of metal-based chromophores for sustainable chemical transformations.