Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Rapid and Sustainable Electrochemical Pd Catalyst Generation from Bulk Metal. / Самойленко, Дмитрий Евгеньевич; Лоцман, Кристина Александровна; Родыгин, Константин Сергеевич; Анаников, Валентин Павлович.
в: Chemistry - A European Journal, Том 31, № 11, e202403872, 28.01.2025.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Rapid and Sustainable Electrochemical Pd Catalyst Generation from Bulk Metal
AU - Самойленко, Дмитрий Евгеньевич
AU - Лоцман, Кристина Александровна
AU - Родыгин, Константин Сергеевич
AU - Анаников, Валентин Павлович
PY - 2025/1/28
Y1 - 2025/1/28
N2 - Palladium catalysts form a cornerstone of modernchemistry with upmost scientific and industrial impact. Bulkpalladium metal itself is chemically inert, and a sequence ofchemical transformations has to be utilized to convert the metal intoPd pre-catalyst covered by ligands. However, the “cocktail” ofcatalysis concept discovered recently has shown that Pd systemscan efficiently operate in catalysis without the necessity of acomplicated and expensive pre-installed ligand environment. Here,we point out on a green and sustainable process for Pd activespecies generation without the need of waste-abundant pre-catalystrelatedchemistry. In this work, an electric current was used togenerate an active Pd catalyst from a bulk metal in an ionic liquidmedium for the efficient cross-coupling of aryl iodides/bromides andboronic acids. Synthetically important Suzuki cross-coupling wasutilized as a representative test reaction to confirm the idea. It shouldbe emphasized that electric current is used only at the Pd dissolutionstage. Afterwards, the electrodes are removed from the reactionmixture and a standard reaction procedure can be followed. Thereported catalyst preparation process via electrochemical dissolutionis potentially compatible with a number of already existing catalyticmethods.
AB - Palladium catalysts form a cornerstone of modernchemistry with upmost scientific and industrial impact. Bulkpalladium metal itself is chemically inert, and a sequence ofchemical transformations has to be utilized to convert the metal intoPd pre-catalyst covered by ligands. However, the “cocktail” ofcatalysis concept discovered recently has shown that Pd systemscan efficiently operate in catalysis without the necessity of acomplicated and expensive pre-installed ligand environment. Here,we point out on a green and sustainable process for Pd activespecies generation without the need of waste-abundant pre-catalystrelatedchemistry. In this work, an electric current was used togenerate an active Pd catalyst from a bulk metal in an ionic liquidmedium for the efficient cross-coupling of aryl iodides/bromides andboronic acids. Synthetically important Suzuki cross-coupling wasutilized as a representative test reaction to confirm the idea. It shouldbe emphasized that electric current is used only at the Pd dissolutionstage. Afterwards, the electrodes are removed from the reactionmixture and a standard reaction procedure can be followed. Thereported catalyst preparation process via electrochemical dissolutionis potentially compatible with a number of already existing catalyticmethods.
KW - Electrochemical metal dissolution
KW - Electrochemistry
KW - Ionic liquids
KW - Pd catalysis
KW - Suzuki cross-coupling
UR - https://www.mendeley.com/catalogue/abe67e90-458c-3351-bb18-0926094c4824/
U2 - 10.1002/chem.202403872
DO - 10.1002/chem.202403872
M3 - Article
VL - 31
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
SN - 0947-6539
IS - 11
M1 - e202403872
ER -
ID: 126272669