4.5 Review

Synthetic reactions driven by electron-donor-acceptor (EDA) complexes

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 17, 期 -, 页码 771-799

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.17.67

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资金

  1. National Natural Science Foundation of China [21901216]
  2. Fund of Science and Technology Agency of Chengdu [2019YF0900049SN]
  3. Sichuan Institute of Atomic Energy [FZBC2020002]
  4. Fundamental Research Funds for the Central Universities
  5. Sichuan Science and Technology Program [2018HH0090, 2019YFH0032, 2019YJ0548]
  6. Key project of Sichuan Traditional Chinese Medicine Administration [2018HJZX024]
  7. 14th Personalized Experimental Project [GX2020160025]
  8. Irradiation Preservation Technology Key Laboratory of Sichuan Province

向作者/读者索取更多资源

The electron-donor-acceptor (EDA) complex, formed by dipole-dipole interactions between an electron donor and an electron acceptor, can be transformed into the excited state upon light irradiation, leading to electron transfer and subsequent reactions. Reactions involving EDA complexes are typically mild and do not require transition metal catalysts or photosensitizers, aligning with the principles of green chemistry.
The reversible, weak ground-state aggregate formed by dipole?dipole interactions between an electron donor and an electron acceptor is referred to as an electron-donor?acceptor (EDA) complex. Generally, upon light irradiation, the EDA complex turns into the excited state, causing an electron transfer to give radicals and to initiate subsequent reactions. Besides light as an external energy source, reactions involving the participation of EDA complexes are mild, obviating transition metal catalysts or photosensitizers in the majority of cases and are in line with the theme of green chemistry. This review discusses the synthetic reactions concerned with EDA complexes as well as the mechanisms that have been shown over the past five years.

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