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Electron Transport Chain: Complex III and IV01:43

Electron Transport Chain: Complex III and IV

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During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
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The final stage of cellular respiration is oxidative phosphorylation that consists of two steps: the electron transport chain and chemiosmosis. The electron transport chain is a set of proteins found in the inner mitochondrial membrane in eukaryotic cells. Its primary function is to establish a proton gradient that can be used during chemiosmosis to produce ATP and generate electron carriers, such as NAD+ and FAD, that are used in glycolysis and the citric acid cycle.
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Electron Transport Chain: Complex I and II01:46

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The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
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Carbocations02:10

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Carbocations are one of the reaction intermediates formed during several nucleophilic substitutions or elimination reactions. A carbocation is an electron-deficient species with the central carbon atom having six electrons and three bonded atoms. The central carbon in a carbocation is sp2 hybridized with trigonal planar geometry. It has an empty p orbital perpendicular to the plane of the structure that can accept electrons. Thus, carbocations act as strong electrophiles and may react with any...
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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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The mitochondrial cristae membrane is the primary site for the oxidative phosphorylation (OXPHOS) process of energy conversion mediated through respiratory complexes I to V. These complexes have been widely studied for decades, and it has been proven that they form supramolecular structures called respiratory supercomplexes (SC). These higher-order complexes may be crucial in maintaining the biochemical structure and improving the physiological activity of the individual complexes while...
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Related Experiment Video

Updated: Jul 11, 2025

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
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Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron

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A Triplet Iron Carbyne Complex.

Jiahao Rao1, Shicheng Dong2, Chengbo Yang1

  • 1State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.

Journal of the American Chemical Society
|November 16, 2023
PubMed
Summary

Researchers synthesized the first triplet metal terminal carbyne, an iron cyclic carbyne complex. This breakthrough challenges previous low-spin state limitations for metal carbynes, opening new avenues in synthesis and material science.

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Area of Science:

  • Organometallic Chemistry
  • Inorganic Chemistry

Background:

  • Metal carbynes are crucial in organic synthesis and material science.
  • Typically, metal carbynes exhibit low-spin ground states (S = 0 or 1/2) due to the strong field nature of carbyne ligands.
  • Tuning the spin state of metal carbynes remains a significant challenge.

Purpose of the Study:

  • To synthesize and characterize the first triplet metal terminal carbyne.
  • To explore the unique properties and reactivity of triplet metal carbynes.

Main Methods:

  • Synthesis via oxidative addition of a low-coordinate iron(0) N-heterocyclic carbene complex with a thioazole-2-ylidene C-S bond.
  • Characterization of the resulting iron cyclic carbyne complex.

Main Results:

  • Successfully synthesized the first triplet (S = 1) metal terminal carbyne, an iron cyclic carbyne complex.
  • The complex features an LXZ-type carbyne ligand and a weak Fe≡C triple bond.
  • Exhibits unique reactivity, including facile carbyne coupling, weak nucleophile affinity, and facial addition with electrophiles.

Conclusions:

  • This work provides the first example of a triplet metal terminal carbyne.
  • The novel iron cyclic carbyne complex demonstrates distinct reactivity compared to classical metal carbynes.
  • Opens new possibilities for metal carbynes in catalysis and materials.