Water-stabilized three- and four-atom palladium clusters as highly active catalytic species in ligand-free C-C cross-coupling reactions.

Angew Chem Int Ed Engl

Instituto de Tecnología Química, Universidad Politécnica de Valencia-Consejo Superior de Investigaciones Científicas, Avda. de los Naranjos s/n, 46022 Valencia (Spain).

Published: October 2013

Elite cliques: Palladium clusters with three and four atoms were found to be the catalytically active species for ligand-free palladium-catalyzed CC bond-forming reactions. These palladium cluster species could be stabilized in water and stored for long periods of time for use on demand with no loss of activity. High yields of products and turnover frequencies (TOFs) of up to 10(5)  h(-1) were observed.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201303188DOI Listing

Publication Analysis

Top Keywords

palladium clusters
8
species ligand-free
8
water-stabilized three-
4
three- four-atom
4
four-atom palladium
4
clusters highly
4
highly active
4
active catalytic
4
catalytic species
4
ligand-free c-c
4

Similar Publications

Phenylacetylene is a detrimental impurity in the polymerisation of styrene, capable of poisoning catalysts even at ppm levels and significantly degrading the quality of polystyrene. The semi-hydrogenation of phenylacetylene to styrene instead of ethylbenzene is, therefore, an important industrial process. We report a novel cerium(iv)-based metal-organic framework (denoted as Ce-bptc), which comprises {Ce} clusters bridged by biphenyl-3,3',5,5'-tetracarboxylate linkers.

View Article and Find Full Text PDF
Article Synopsis
  • The manuscript presents a novel palladium-catalyzed cyclization method using carboxylic acids and terminal alkynes, which showcases its potential for creating complex organic molecules.
  • This technique is significant as it allows carboxylic acids, traditionally underutilized, to serve as effective building blocks in intramolecular cycloaddition and addresses long-standing challenges in synthesizing substituted naphthalenes.
  • The reaction demonstrates a wide range of substrate compatibility and functional group tolerance, making it applicable for scalable synthesis in organic chemistry, drug discovery, and material science.
View Article and Find Full Text PDF

The sustainable and affordable environmental application of Pd catalysis needs further improvement of Pd mass activity. Besides the well-recognized importance of physical utilization efficiency─the ratio of surface atoms forming reactant-accessible reactive sites─a lesser-known fact is that the congestion of these reactive sites, which we term as the chemical utilization efficiency, also influences the mass activity. Herein, by leveraging the 100% physical utilization efficiency of a fully exposed Pd cluster (Pd) and the hydrogenation activity of TiNiN, we developed Pd/TiNiN as a high physical and chemical utilization efficiency catalyst.

View Article and Find Full Text PDF

In this study, we present a comprehensive approach for the morphological analysis of palladium on carbon (Pd/C) nanoparticles utilizing scanning electron microscopy (SEM) imaging and advanced deep learning techniques. A deep learning detection model based on an attention mechanism was implemented to accurately identify and delineate small nanoparticles within unlabeled SEM images. Following detection, a graph-based network was employed to analyze the structural characteristics of the nanoparticles, while density-based spatial clustering of applications with noise was utilized to cluster the detected nanoparticles, identifying meaningful patterns and distributions.

View Article and Find Full Text PDF

Using density functional theory, we carefully calculated the relative stability of monolayer, few-layer, and cluster structures with Penta PdSe, T-phase PdSe, and PdSe-phase. We found that the stability of Penta PdSe increases with the number of layers. The Penta PdSe, T-phase PdSe, and PdSe monolayers are all semiconducting, with band gaps of 1.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!