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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 изданияхстатьяРецензирование

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@article{5c59bcb4b4d548da8535c34bac36eff1,
title = "Rapid and Sustainable Electrochemical Pd Catalyst Generation from Bulk Metal",
abstract = "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.",
keywords = "Electrochemical metal dissolution, Electrochemistry, Ionic liquids, Pd catalysis, Suzuki cross-coupling",
author = "Самойленко, {Дмитрий Евгеньевич} and Лоцман, {Кристина Александровна} and Родыгин, {Константин Сергеевич} and Анаников, {Валентин Павлович}",
year = "2025",
month = jan,
day = "28",
doi = "10.1002/chem.202403872",
language = "English",
volume = "31",
journal = "Chemistry - A European Journal",
issn = "0947-6539",
publisher = "Wiley-Blackwell",
number = "11",

}

RIS

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