Ligand-Enabled Photocatalytic Reactivity of Iron(III) Halide Salts with Cyan and Green Light

Iron(III) halide salts have emerged as cheap and efficient catalysts for photocatalytic transformations, including C-H alkylation, C-H and alkene oxidation, azidation/amination, and others. The majority of these methods require UV light (λ ≤ 390 nm), and systematic efforts to enable the use of lower-energy visible light remain valuable. We report the use of simple Fe(III) salts that enable C-H functionalizations with longer wavelength visible light up to 525 nm (green light). The one-pot conversion of aldehydes to amides, esters, and ketones as well as direct alkylation are described using blue, cyan, and green light.

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Publication Details

Journal
Organic Letters
Published
2026-01-14
DOI
https://doi.org/10.1021/acs.orglett.5c04928
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Ligand-Enabled Photocatalytic Reactivity of Iron(III) Halide Salts with Cyan and Green Light

Mikayla M. Wymore, David B.C. Martin
Organic Letters
Radical Photochemical Reactions
article

Ligand-Enabled Photocatalytic Reactivity of Iron(III) Halide Salts with Cyan and Green Light

Mikayla M. Wymore, David B.C. Martin
article en

Abstract

Iron(III) halide salts have emerged as cheap and efficient catalysts for photocatalytic transformations, including C-H alkylation, C-H and alkene oxidation, azidation/amination, and others. The majority of these methods require UV light (λ ≤ 390 nm), and systematic efforts to enable the use of lower-energy visible light remain valuable. We report the use of simple Fe(III) salts that enable C-H functionalizations with longer wavelength visible light up to 525 nm (green light). The one-pot conversion of aldehydes to amides, esters, and ketones as well as direct alkylation are described using blue, cyan, and green light.

Organic LettersVol. 28(4)
University of Iowa (US)
Affordable and clean energy
Openalex Percentile: Top 89%
Radical Photochemical Reactions
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