Closing the Loop: Low‐Waste Phosphorus Functionalization Enabled by Simple Disulfides

Useful monophosphorus products are obtained from both white and red phosphorus via a simple strategy involving initial oxidation by aryl disulfides followed by quenching with nucleophiles. Direct transformations of elemental phosphorus are usually very challenging, forcing chemists to instead rely on inefficient and hazardous multi-step methods. However, here they are achieved using inexpensive and easy-to-handle reagents, providing access to diverse P-C, P-N and P-O bonded products in good yields. By isolating the thiolate byproducts of these reactions, a simple, closed loop can be achieved that produces only minimal, benign waste byproducts, in contrast to other direct methods. This closed loop can even be elaborated into a true (electro)catalytic cycle, which is extremely rare in the field of elemental phosphorus functionalization.

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Publication Details

Journal
ChemSusChem
Published
2024-11-11
DOI
https://doi.org/10.1002/cssc.202401895
Citations
2
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.50

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article

Closing the Loop: Low‐Waste Phosphorus Functionalization Enabled by Simple Disulfides

Thomas M. Horsley Downie, Daniel J. Scott, Robert Wolf, Ajdin Velić et al.
2 citations
ChemSusChem
Chemical Synthesis and Reactions
0.50
article

Closing the Loop: Low‐Waste Phosphorus Functionalization Enabled by Simple Disulfides

Thomas M. Horsley Downie, Daniel J. Scott, Robert Wolf, Ajdin Velić, Luiza Beatriz Monteiro Coelho
article en
2 citations

Abstract

Useful monophosphorus products are obtained from both white and red phosphorus via a simple strategy involving initial oxidation by aryl disulfides followed by quenching with nucleophiles. Direct transformations of elemental phosphorus are usually very challenging, forcing chemists to instead rely on inefficient and hazardous multi-step methods. However, here they are achieved using inexpensive and easy-to-handle reagents, providing access to diverse P-C, P-N and P-O bonded products in good yields. By isolating the thiolate byproducts of these reactions, a simple, closed loop can be achieved that produces only minimal, benign waste byproducts, in contrast to other direct methods. This closed loop can even be elaborated into a true (electro)catalytic cycle, which is extremely rare in the field of elemental phosphorus functionalization.

ChemSusChemVol. 18(7)
University of Strathclyde (GB), University of Bath (GB), University of Regensburg (DE)
Alexander von Humboldt-Stiftung, University of Bath, Deutscher Akademischer Austauschdienst, Deutsche Forschungsgemeinschaft, Engineering and Physical Sciences Research Council, Elitenetzwerk Bayern, HORIZON EUROPE European Research Council
Openalex Percentile: Top 38%
Chemical Synthesis and Reactions
0.50
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