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

**Authors:** Mikayla M. Wymore, David B.C. Martin

PMC · DOI: 10.1021/acs.orglett.5c04928 · Organic Letters · 2026-01-14

## TL;DR

This paper shows how iron(III) salts can be used with visible light, including green light, to perform chemical reactions that typically require UV light.

## Contribution

The study introduces a new method to use longer wavelength visible light with iron(III) salts for photocatalytic C–H functionalizations.

## Key findings

- Iron(III) salts enable C–H functionalizations using visible light up to 525 nm.
- Aldehydes can be converted to amides, esters, and ketones using blue, cyan, and green light.
- The method allows for direct alkylation under visible light conditions.

## 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.

## Linked entities

- **Chemicals:** aldehydes (PubChem CID 6449839)

## Full-text entities

- **Diseases:** LMCT (MESH:D058747)
- **Chemicals:** C (MESH:D002244), benzamide (MESH:C037689), chlorine (MESH:D002713), TBA[FeClBr3] (1c (-), ester (MESH:D004952), iron salts (MESH:C000499), N-chlorosuccinimide (MESH:C015752), mesitylene (MESH:C010219), TiO2 (MESH:C009495), 1,1,1,3,3,3-hexafluoroisopropanol (MESH:C001337), benzaldehydes (MESH:D001547), amine (MESH:D000588), TEMPO (MESH:C003959), acetamide (MESH:C030686), polymer (MESH:D011108), dibromomethane (MESH:C027947), halogen (MESH:D006219), CH3CN (MESH:C032159), HBr (MESH:D018054), Phenol (MESH:D019800), alkene (MESH:D000475), N2 (MESH:D009584), NBS (MESH:D009556), oxygen (MESH:D010100), Aniline (MESH:C023650), Fe (MESH:D007501), H (MESH:D006859), benzylamine (MESH:C030796), carvone (MESH:C006923), ferrate (MESH:C017311), benzoyl chloride (MESH:C013409), p-Anisaldehyde (MESH:C024896), pyridine (MESH:C023666), trichloroisocyanuric acid (MESH:C557580), potassium ferrioxalate (MESH:C034942), acetaldehyde (MESH:D000079), alcohol (MESH:D000438), Aldehyde (MESH:D000447), Benzaldehyde (MESH:C032175), beta-alanine methyl ester (MESH:C018596), carboxylic acid (MESH:D002264), peroxide (MESH:D010545), bromide (MESH:D001965), FeCl3 (MESH:C024555), hexanal (MESH:C010463), amide (MESH:D000577), benzyl alcohol (MESH:D019905), THF (MESH:C018674), 13C (MESH:C000615229), Br (MESH:D001966), tryptamine (MESH:C030820), Ketone (MESH:D007659), tetra-n-butylammonium (MESH:C009405)
- **Mutations:** A 1  C

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12865799/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12865799/full.md

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Source: https://tomesphere.com/paper/PMC12865799