Abstract

Light can be considered an ideal reagent for environmentally friendly, 'green' chemical synthesis; unlike many conventional reagents, light is non-toxic, generates no waste, and can be obtained from renewable sources. Nevertheless, the need for high-energy ultraviolet radiation in most organic photochemical processes has limited both the practicality and environmental benefits of photochemical synthesis on industrially relevant scales. This perspective describes recent approaches to the use of metal polypyridyl photocatalysts in synthetic organic transformations. Given the remarkable photophysical properties of these complexes, these new transformations, which use Ru(bpy)(3)(2+) and related photocatalysts, can be conducted using almost any source of visible light, including both store-bought fluorescent light bulbs and ambient sunlight. Transition metal photocatalysis thus represents a promising strategy towards the development of practical, scalable industrial processes with great environmental benefits.

Keywords

PhotocatalysisChemistryPhotochemistryVisible spectrumReagentEnvironmentally friendlyUltraviolet lightNanotechnologyGreen chemistryOrganic synthesisRenewable energyBiochemical engineeringCombinatorial chemistryCatalysisOrganic chemistryReaction mechanismOptoelectronicsMaterials science

MeSH Terms

CatalysisLightOrganometallic CompoundsOxidation-ReductionPhotochemical ProcessesTransition Elements

Affiliated Institutions

Related Publications

Photoredox Catalysis with Visible Light

On the sunny side: Recent examples of visible-light-promoted photoredox catalysis in the presence of [Ru(bpy)3]2+ as an efficient photocatalyst have set new standards for conduc...

2009 Angewandte Chemie International Edition 973 citations

Publication Info

Year
2010
Type
article
Volume
2
Issue
7
Pages
527-532
Citations
2563
Access
Closed

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2563
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2
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2492
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Cite This

Tehshik P. Yoon, Michael A. Ischay, Juana Du (2010). Visible light photocatalysis as a greener approach to photochemical synthesis. Nature Chemistry , 2 (7) , 527-532. https://doi.org/10.1038/nchem.687

Identifiers

DOI
10.1038/nchem.687
PMID
20571569

Data Quality

Data completeness: 81%