Visible-light-driven photocatalytic carboxylation to aromatic carboxylic acids with CO
(Hetero)aromatic carboxylic acids and their derivatives attract attention due to their role in the synthesis of several biologically active molecules, active pharmaceutical ingredients, polymers, etc . Carbon dioxide (CO 2 ) is a prime C1 source for the synthesis of aromatic carboxylic acids because...
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Veröffentlicht in: | Organic & biomolecular chemistry 2024-01, Vol.22 (4), p.682-693 |
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Zusammenfassung: | (Hetero)aromatic carboxylic acids and their derivatives attract attention due to their role in the synthesis of several biologically active molecules, active pharmaceutical ingredients, polymers,
etc
. Carbon dioxide (CO
2
) is a prime C1 source for the synthesis of aromatic carboxylic acids because of its nontoxicity, nonflammability, abundance and renewability. Owing to the thermodynamic and chemical inertness of CO
2
, traditional carboxylation to aromatic carboxylic acids with CO
2
is always performed under harsh reaction conditions or using stoichiometric metallic reductants. Visible-light-driven carboxylation with CO
2
provides an environmentally benign, mild, and high-efficiency route for the production of aromatic carboxylic acids. This review comprehensively introduces the visible-light-driven preparation of aromatic carboxylic acids through a visible-light-driven oxidative addition and reductive elimination mechanism, binding of aryl (radical) anions which are produced by photoinduced electron transfer (PET) to CO
2
, binding of carbon dioxide anion radicals (CO
2
&z.rad;
−
) which are formed by PET to aryl compounds, radical coupling between CO
2
&z.rad;
−
and aryl radicals, and other mechanisms. Finally, this review provides a summary and the future work direction. This article offers a theoretical guidance for efficient synthesis of aromatic carboxylic acids
via
photocatalysis.
The manuscript first reviews the preparation of valuable aromatic carboxylic acids by visible-light-driven carboxylation with CO
2
. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d3ob01788e |