Advancements in Pd-Based Supported Porous Nanocatalysts for the C-C Cross-Coupling Reactions DOI Open Access
Debabrata Chakraborty, Asim Bhaumik

Catalysts, Год журнала: 2024, Номер 15(1), С. 16 - 16

Опубликована: Дек. 28, 2024

Palladium (Pd) is a 4d transition metal with electronic configuration [Kr] 4d10 5s0, and it one of the most widely studied metals in periodic table due to its versatile catalytic role organic synthesis. The choice ligands that can coordinate Pd sites plays crucial progress reaction. Due coexistence multiple oxidation states (Pd(0)/Pd(II)), active catalysts participate various stages coupling Pd-catalyzed C-C reactions proceed through four steps: (1) oxidative addition reactant site, (2) transmetallation, (3) rearrangements ligand centers (4) reductive elimination products. For heterogeneous nanocatalysts, are often strongly bound (chelated) solid catalyst surfaces. In this review, we have highlighted advancements made nanocatalysts an emphasis on types different classes porous solids, which could ligate via strong covalent bonds. high specific surface areas small these provide larger number thus facilitate Mechanistic aspects cross-coupling discussed context structure–reactivity relationship.

Язык: Английский

Highly ordered Periodic Mesoporous Organosilica material containing the ionic 4,4-bipyridinium group and decorated with palladium nanoparticles: A proposal for nanoreactor DOI

Cezar A. Didó,

Carlos D.G. Caneppele,

Douglas Santana Charqueiro

и другие.

Catalysis Today, Год журнала: 2024, Номер 444, С. 115016 - 115016

Опубликована: Авг. 27, 2024

Язык: Английский

Процитировано

0

Pd nanoparticle supported on N‐doped carbon derived from sodium alginate/melamine blends as efficient heterogeneous catalyst for Heck reactions DOI
Jie Zhou, Yuanyuan Wu, Yonghong Liu

и другие.

ChemCatChem, Год журнала: 2024, Номер unknown

Опубликована: Сен. 5, 2024

Abstract N‐doped porous carbon shows great potential in the field of heterogenous supports due to its high porosity, large surface area, rich active sites, and strong chelation with catalytic metals species. Herein, we successfully prepared a novel derived from sodium alginate/melamine blends (SAMNC) different mass ratio through simple carbonization activation process. Hierarchical structure has been confirmed SEM, TEM, N 2 adsorption characterization. After Na PdCl 4 solution impregnation further reduction process, Pd 0 nanoparticles have uniformly immobilized on SAMNC support produce Pd@SAMNC catalyst. The optimal Pd@SAMNC‐0.6 possesses content (5.13%), (5.90%), BET specific area 1884.5 m ·g −1 . Positron annihilation lifetime spectroscopy (PALS) investigation materials provided sub‐nano level microporous information proofs had capability provide more sites for reactions than commercial supported activated (Pd@AC). catalyst showed superior efficiency Heck coupling reaction between aromatic halides alkenes can be recycled 17 runs without significant decrease efficiency.

Язык: Английский

Процитировано

0

Advancements in Pd-Based Supported Porous Nanocatalysts for the C-C Cross-Coupling Reactions DOI Open Access
Debabrata Chakraborty, Asim Bhaumik

Catalysts, Год журнала: 2024, Номер 15(1), С. 16 - 16

Опубликована: Дек. 28, 2024

Palladium (Pd) is a 4d transition metal with electronic configuration [Kr] 4d10 5s0, and it one of the most widely studied metals in periodic table due to its versatile catalytic role organic synthesis. The choice ligands that can coordinate Pd sites plays crucial progress reaction. Due coexistence multiple oxidation states (Pd(0)/Pd(II)), active catalysts participate various stages coupling Pd-catalyzed C-C reactions proceed through four steps: (1) oxidative addition reactant site, (2) transmetallation, (3) rearrangements ligand centers (4) reductive elimination products. For heterogeneous nanocatalysts, are often strongly bound (chelated) solid catalyst surfaces. In this review, we have highlighted advancements made nanocatalysts an emphasis on types different classes porous solids, which could ligate via strong covalent bonds. high specific surface areas small these provide larger number thus facilitate Mechanistic aspects cross-coupling discussed context structure–reactivity relationship.

Язык: Английский

Процитировано

0