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Maria Sara Raju1, Maxime Aragon-Alberti1, Kevin Cardenas1

  • 1Laboratoire National des Champs Magnétiques Intenses, CNRS, Université Grenoble Alpes, INSA Toulouse, Université Toulouse Paul Sabatier, EMFL, F-38042 Grenoble, France.

ACS central science
|July 29, 2025
PubMed
概括

磁性性光化学 (MChPh) 可以诱导分子中的反体过量 (ee). 这项研究重新探索了MChPh,实现了0.50% ee,超过了循环极化光化学.

相关概念视频

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Photochemical Electrocyclic Reactions: Stereochemistry

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.
Selection Rules: Photochemical Activation
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Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
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Thermal and Photochemical Electrocyclic Reactions: Overview

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