Unprecedented Mo3S4 cluster-catalyzed radical C-C cross-coupling reactions of aryl alkynes and acrylates
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Otros documentos de la autoría: Mateu-Campos, Juanjo; Guillamón, Eva; Safont Villarreal, Vicent Sixte; Junge, Kathrin; Junge, Henrik; Beller, matthias; Llusar, Rosa
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7013
comunitat-uji-handle3:10234/8638
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Título
Unprecedented Mo3S4 cluster-catalyzed radical C-C cross-coupling reactions of aryl alkynes and acrylatesAutoría
Fecha de publicación
2024-01-30Editor
Royal Society of ChemistryCita bibliográfica
MATEU-CAMPOS, Juanjo, et al. Unprecedented Mo 3 S 4 cluster-catalyzed radical C–C cross-coupling reactions of aryl alkynes and acrylates. Dalton Transactions, 2024, vol. 53, no 9, p. 4147-4153.Tipo de documento
info:eu-repo/semantics/articleVersión
info:eu-repo/semantics/publishedVersionPalabras clave / Materias
Resumen
A new method for the generation of benzyl radicals from terminal aromatic alkynes has been developed, which allows the direct cross coupling with acrylate derivatives. Our additive-free protocol employs air-stable ... [+]
A new method for the generation of benzyl radicals from terminal aromatic alkynes has been developed, which allows the direct cross coupling with acrylate derivatives. Our additive-free protocol employs air-stable diamino Mo3S4 cubane-type cluster catalysts in the presence of hydrogen. A sulfur-centered cluster catalysis mechanism for benzyl radical formation is proposed based on catalytic and stoichiometric experiments. The process starts with the cluster hydrogen activation to form a bis(hydrosulfido) [Mo3(μ3-S)(μ-S)(μ-SH)2Cl3(dmen)3]+ intermediate. The reaction of various aromatic terminal alkynes containing different functionalities with a series of acrylates affords the corresponding Giese-type radical addition products. [-]
Entidad financiadora
Ministerio de Ciencia, Innovación y Universidades (Spain) | Generalitat Valenciana | Universitat Jaume I
Código del proyecto o subvención
PID2022-141089NB-I00 | CIAICO/2021/122 | UJI-B2021-29 | UJI-B2022-56 | E-2022-31
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© The Royal Society of Chemistry 2024
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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