ChemInform Abstract: Pd(L-Proline)2Complex: An Efficient Catalyst for Suzuki-Miyaura Coupling Reaction in Neat Water.

ChemInform ◽  
2014 ◽  
Vol 45 (42) ◽  
pp. no-no
Author(s):  
Guofu Zhang ◽  
Yuxin Luan ◽  
Xingwang Han ◽  
Yong Wang ◽  
Xin Wen ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Efficient Catalyst ◽  
Neat Water

Pd(l-proline)2complex: an efficient catalyst for Suzuki-Miyaura coupling reaction in neat water

2014 ◽  
Vol 28 (5) ◽  
pp. 332-336 ◽  
Author(s):  
Guofu Zhang ◽  
Yuxin Luan ◽  
Xingwang Han ◽  
Yong Wang ◽  
Xin Wen ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Efficient Catalyst ◽  
Neat Water

A highly efficient catalyst of a nitrogen-based ligand for the Suzuki coupling reaction at room temperature under air in neat water

2014 ◽  
Vol 12 (25) ◽  
pp. 4511-4516 ◽  
Author(s):  
Shiwen Liu ◽  
Meiyun Lv ◽  
Daoan Xiao ◽  
Xiaogang Li ◽  
Xiuling Zhou ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Room Temperature ◽  
Coupling Reaction ◽  
Suzuki Coupling ◽  
Water Soluble ◽  
Efficient Catalyst ◽  
Suzuki Coupling Reaction ◽  
Highly Efficient ◽  
Neat Water

Glycine is used to prepare an air-stable and water-soluble catalyst for the Suzuki–Miyaura reaction. In the presence of 0.1% [PdCl2(NH2CH2COOH)2], excellent catalytic activity is observed at room temperature under air in neat water.

An easily prepared palladium-hydrogel nanocomposite catalyst for C–C coupling reactions

2014 ◽  
Vol 2 (44) ◽  
pp. 18952-18958 ◽  
Author(s):  
Mitasree Maity ◽  
Uday Maitra
Keyword(s):  
Palladium Nanoparticles ◽  
Room Temperature ◽  
Coupling Reaction ◽  
Coupling Reactions ◽  
Sodium Cyanoborohydride ◽  
Efficient Catalyst ◽  
Suzuki Coupling Reaction ◽  
Reaction In Water ◽  
Hydrogel Nanocomposite

Palladium nanoparticles were efficiently prepared in situ by sodium cyanoborohydride reduction of Pd(ii) at room temperature using calcium-cholate hydrogel fibers as templates. The PdNPs self-organize on the gel fibers, which supports the controlled growth as well as stabilization of PdNPs. The hybrid xerogel was used as an efficient catalyst for the Suzuki coupling reaction in water.

scholarly journals A New Heterogeneous Catalyst Obtained via Supramolecular Decoration of Graphene with a Pd2+ Azamacrocyclic Complex

Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2714 ◽  
Author(s):  
Matteo Savastano ◽  
Paloma Arranz-Mascarós ◽  
Maria Paz Clares ◽  
Rafael Cuesta ◽  
Maria Luz Godino-Salido ◽  
...  
Keyword(s):  
Heterogeneous Catalyst ◽  
Self Assembly ◽  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Assembly Process ◽  
Efficient Catalyst ◽  
Mild Conditions ◽  
Cross Coupling Reaction ◽  
Green Procedure

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditions (50 °C, water, aerobic atmosphere, 14 h). The catalyst proved to be reusable for at least four cycles, although decreasing yields down to 50% were observed.

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