Recoverable palladium catalysts for Suzuki-Miyaura cross-coupling reactions based on organic-inorganic hybrid silica materials containing imidazolium and dihydroimidazolium salts

Montserrat Trilla; Guadalupe Borja; Roser Pleixats; Michel Wong Chi Man; Catherine Bied; Joël J.E. Moreau

doi:10.1002/adsc.200800455

Recoverable palladium catalysts for Suzuki-Miyaura cross-coupling reactions based on organic-inorganic hybrid silica materials containing imidazolium and dihydroimidazolium salts

Montserrat Trilla, Guadalupe Borja, Roser Pleixats, Michel Wong Chi Man, Catherine Bied, Joël J.E. Moreau

Departamento de Química

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

45 Citas (Scopus)

Resumen

The systems formed by palladium acetate [Pd(OAc)2] and hybrid silica materials prepared by sol-gel from monosilylated imidazolium and disilylated dihydroimidazolium salts show catalytic activity in Suzuki-Miyaura cross-couplings with challenging aryl bromides and chlorides. They are very efficient as recoverable catalysts with aryl bromides. Recycling is also possible with aryl chlorides, although with lower conversions. In situ formation of palladium nanoparticles has been observed in recycling experiments. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

Idioma original	Inglés
Páginas (desde-hasta)	2566-2574
Publicación	Advanced Synthesis and Catalysis
Volumen	350
N.º	16
DOI	https://doi.org/10.1002/adsc.200800455
Estado	Publicada - 3 nov 2008

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title = "Recoverable palladium catalysts for Suzuki-Miyaura cross-coupling reactions based on organic-inorganic hybrid silica materials containing imidazolium and dihydroimidazolium salts",

abstract = "The systems formed by palladium acetate [Pd(OAc)2] and hybrid silica materials prepared by sol-gel from monosilylated imidazolium and disilylated dihydroimidazolium salts show catalytic activity in Suzuki-Miyaura cross-couplings with challenging aryl bromides and chlorides. They are very efficient as recoverable catalysts with aryl bromides. Recycling is also possible with aryl chlorides, although with lower conversions. In situ formation of palladium nanoparticles has been observed in recycling experiments. {\textcopyright} 2008 Wiley-VCH Verlag GmbH & Co. KGaA.",

keywords = "Catalyst recycling, Nanoparticles, Organic-inorganic hybrid composites, Palladium, Sol-gel processes, Suzuki-Miyaura reaction",

author = "Montserrat Trilla and Guadalupe Borja and Roser Pleixats and Man, {Michel Wong Chi} and Catherine Bied and Moreau, {Jo{\"e}l J.E.}",

year = "2008",

month = nov,

day = "3",

doi = "10.1002/adsc.200800455",

language = "English",

volume = "350",

pages = "2566--2574",

journal = "Advanced Synthesis and Catalysis",

issn = "1615-4150",

number = "16",

}

Recoverable palladium catalysts for Suzuki-Miyaura cross-coupling reactions based on organic-inorganic hybrid silica materials containing imidazolium and dihydroimidazolium salts. / Trilla, Montserrat; Borja, Guadalupe; Pleixats, Roser et al.
En: Advanced Synthesis and Catalysis, Vol. 350, N.º 16, 03.11.2008, p. 2566-2574.

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

TY - JOUR

T1 - Recoverable palladium catalysts for Suzuki-Miyaura cross-coupling reactions based on organic-inorganic hybrid silica materials containing imidazolium and dihydroimidazolium salts

AU - Trilla, Montserrat

AU - Borja, Guadalupe

AU - Pleixats, Roser

AU - Man, Michel Wong Chi

AU - Bied, Catherine

AU - Moreau, Joël J.E.

PY - 2008/11/3

Y1 - 2008/11/3

N2 - The systems formed by palladium acetate [Pd(OAc)2] and hybrid silica materials prepared by sol-gel from monosilylated imidazolium and disilylated dihydroimidazolium salts show catalytic activity in Suzuki-Miyaura cross-couplings with challenging aryl bromides and chlorides. They are very efficient as recoverable catalysts with aryl bromides. Recycling is also possible with aryl chlorides, although with lower conversions. In situ formation of palladium nanoparticles has been observed in recycling experiments. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

AB - The systems formed by palladium acetate [Pd(OAc)2] and hybrid silica materials prepared by sol-gel from monosilylated imidazolium and disilylated dihydroimidazolium salts show catalytic activity in Suzuki-Miyaura cross-couplings with challenging aryl bromides and chlorides. They are very efficient as recoverable catalysts with aryl bromides. Recycling is also possible with aryl chlorides, although with lower conversions. In situ formation of palladium nanoparticles has been observed in recycling experiments. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

KW - Catalyst recycling

KW - Nanoparticles

KW - Organic-inorganic hybrid composites

KW - Palladium

KW - Sol-gel processes

KW - Suzuki-Miyaura reaction

U2 - 10.1002/adsc.200800455

DO - 10.1002/adsc.200800455

M3 - Article

SN - 1615-4150

VL - 350

SP - 2566

EP - 2574

JO - Advanced Synthesis and Catalysis

JF - Advanced Synthesis and Catalysis

IS - 16

ER -

Recoverable palladium catalysts for Suzuki-Miyaura cross-coupling reactions based on organic-inorganic hybrid silica materials containing imidazolium and dihydroimidazolium salts

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