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Ligand-Enabled Photocatalytic Reactivity of Iron(III) Halide Salts with Cyan and Green Light
Journal article   Open access   Peer reviewed

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

Mikayla M Wymore and David B C Martin
Organic letters, Vol.28(4), pp.1200-1206
01/14/2026
DOI: 10.1021/acs.orglett.5c04928
PMCID: PMC12865799
PMID: 41534038
url
https://doi.org/10.1021/acs.orglett.5c04928View
Published (Version of record) Open Access

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.
Alcohols Aldehydes Catalysts Electromagnetic radiation Hydrocarbons UIOWA OA Agreement

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