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231226s2023 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202300760
|2 doi
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|a pubmed24n1225.xml
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|a eng
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| 100 |
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|a Wang, Yulei
|e verfasserin
|4 aut
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|a Electrochemical Syntheses of Polycyclic Aromatic Hydrocarbons (PAHs)
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|c 2023
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|a Date Revised 08.12.2023
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a © 2023 The Authors. Advanced Materials published by Wiley-VCH GmbH.
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|a Polycyclic aromatic hydrocarbons (PAHs) have surfaced as increasingly viable components in optoelectronics and material sciences. The development of highly efficient and atom-economic tools to prepare PAHs under exceedingly mild conditions constitutes a long-term goal. Traditional syntheses of PAHs have largely relied on multistep approaches or the conventional Scholl reaction. However, Scholl reactions are largely inefficient with electron-deficient substrates, require stoichiometric chemical oxidants, and typically occur in the presence of strong acid. In sharp contrast, electrochemistry has gained considerable momentum during the past decade as an alternative for the facile and straightforward PAHs assembly, generally via electro-oxidative dehydrogenative annulation, releasing molecular hydrogen as the sole stoichiometric byproduct by the hydrogen evolution reaction. This review provides an overview on the recent and significant advances in the field of electrochemical syntheses of various PAHs until January 2023
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|a Journal Article
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|a Review
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|a CH activation
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| 650 |
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4 |
|a PAHs
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| 650 |
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4 |
|a Scholl reaction
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| 650 |
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4 |
|a electrochemistry
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| 650 |
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4 |
|a electrolysis
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| 700 |
1 |
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|a Zhao, Rong
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Ackermann, Lutz
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 35(2023), 49 vom: 09. Dez., Seite e2300760
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|x 1521-4095
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| 773 |
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|g volume:35
|g year:2023
|g number:49
|g day:09
|g month:12
|g pages:e2300760
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|u http://dx.doi.org/10.1002/adma.202300760
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