ArticleChemSusChem2025
Phenol-Rich Carbon Dots as Metal-Free Nano-Photocatalysts for [3 + 2] Cycloaddition Reactions.
Article in ChemSusChem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Water Permeates and Plasticizes Amorphous Carbon Dots: Unraveling the Inner Accessibility of the Nanoparticles by Glass Transition Studies.Advanced materials (Deerfield Beach, Fla.) · 2026Article
- Going Deep into the Surface Chemistry of Carbon Dots: Influence of Functional Groups on the Redox Abilities.Small (Weinheim an der Bergstrasse, Germany) · 2026Article
- Carbon Dots as Nano-Photocatalysts: A Green Tool for Indole and Heteroarenes Alkylation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Carbon dots (CDs) are unique carbon-based nanoparticles with potential applications in the field of photocatalysis. In this context, the proper selection of precursors and synthetic conditions is of paramount importance when tailoring the photocatalytic features of the resulting nanomaterials. Herein, a novel bottom-up methodology has been developed for the preparation of phenol-rich CDs (Ph-CDs) that allowed us to capitalize on the excellent photoredox properties of surface phenolate anions that can be obtained upon deprotonation of Ph-CDs. Specifically, in this study, Ph-CDs are used in combination with a suitable base and an organocatalyst, namely the Schreiner thiourea (A), to drive valuable [3 + 2] photocycloaddition reactions between suitable cyclopropyl ketones 1 and unsaturated hydrocarbons 2. Mechanistic studies show the key role played by A in the transformation. In fact, this organocatalyst may not only activate the carbonyl moiety of 1 but also stabilize the formation and enhance the photocatalytic performances of phenolate anions on the nanoparticle surfaces. Remarkably, this photocatalytic transformation provides a wide variety of densely functionalized five-membered rings 3 (17 examples, up to 99% yield) under mild operative conditions. Lastly, it is demonstrated that Ph-CDs can be easily recovered and reused up to three times without any significant drop in yield.
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Registered trials
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