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. 2024 Dec;20(52):e2406697.
doi: 10.1002/smll.202406697. Epub 2024 Oct 20.

Molybdenum Disulfide-Based Catalysts in Organic Synthesis: State of the Art, Open Issues, and Future Perspectives

Affiliations

Molybdenum Disulfide-Based Catalysts in Organic Synthesis: State of the Art, Open Issues, and Future Perspectives

Marc Morant-Giner et al. Small. 2024 Dec.

Abstract

In the field of heterogeneous organic catalysis, molybdenum disulfide (MoS2) is gaining increasing attention as a catalytically active material due to its low toxicity, earth abundance, and affordability. Interestingly, the catalytic properties of this metal-based material can be improved by several strategies. In this Perspective, through the analysis of some explicative examples, the main approaches used to prepare highly efficient MoS2-based catalysts in relevant organic reactions are summarized and critically discussed, namely: i) increment of the specific surface area, ii) generation of the metallic 1T phase, iii) introduction of vacancies, iv) preparation of nanostructured hybrids/composites, v) doping with transition metal ions, and vi) partial oxidation of MoS2. Finally, emerging trends in MoS2-based materials catalysis leading to a richer organic synthesis are presented.

Keywords: heterogenous catalysis; molybdenum disulfide; organic chemistry.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Different structural models of 1T and 2H polytypes in MoS2 monolayer. 2H monolayer is also referred to as 1H‐MoS2. Mo: Blue, S: Yellow.
Figure 2
Figure 2
MoS2‐based QDs as heterogeneous photoredox catalysts. a) Photocatalytic cross‐dehydrogenative coupling reactions. b) Photocatalytic synthesis of α‐amino phosphonate derivatives. A: electron acceptor; D: electron donor; Nu: Nucleophile.
Figure 3
Figure 3
MoS2‐based composites materials. a) Photocatalytic aerobic thiocyanation of substituted indoles. b) Ullman type coupling of phenols with iodobenzene.
Figure 4
Figure 4
MoS2‐based nanocomposites materials. a) Catalytic alkylation of substituted indoles with aldehydes and ketones. b) Catalytic alkylation of substituted indoles with nitro alkenes and isatine derivatives.
Figure 5
Figure 5
MoS2‐based metal‐doped materials. a) Selective hydrodeoxygenation of p‐cresol to toluene. b) Hydrodenitrogenation and hydrodesulfurization of heteroarenes under mild operative conditions. Inset: atomic model of doped‐MoS2 single layer. S: yellow, Mo: blue, Co or Ni: orange.

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