Photoelectric properties for aromatic triangular tri-palladium complexes and their catalytic applications in Suzuki-Miyaura coupling reaction

2021 ◽  
Author(s):  
Xujun Li ◽  
Jia Li ◽  
Xiaoshuang Wang ◽  
lingang Wu ◽  
Yanlan Wang ◽  
...  

The photoelectric properties and catalytic activities of substituted triphenylphosphine and sulfur/selenium ligands supported aromatic triangular tri-palladium complexes 1-4, abbreviated as [Pd3]+, were investigated. The cyclic voltammogram of [Pd3]+ in CH3CN-nBu4NPF6...

2014 ◽  
Vol 43 (19) ◽  
pp. 7166-7175 ◽  
Author(s):  
Jin Yang ◽  
Pinhua Li ◽  
Yicheng Zhang ◽  
Lei Wang

Six dinuclear N-heterocyclic carbene–palladium complexes were synthesized from [Pd(μ-Cl)(Cl)(NHC)]2 and Ph2P(CH2)nPPh2, and their catalytic activities towards the Hiyama reaction were investigated.


Author(s):  
Ceren Akpunar ◽  
Namık Özdemir ◽  
Mert Olgun Karataş ◽  
Bülent Alıcı ◽  
İsmail Özdemir Resourches

2022 ◽  
Author(s):  
Márton Nagyházi ◽  
Balázs Almási ◽  
Ádám Lukács ◽  
Attila Bényei ◽  
Tibor Nagy ◽  
...  

A series of bicyclic alkylamino carbenes (BICAAC) (where N-aryl = dipp, mes, 2,6-dimethyl-4-(dimethylamino)phenyl, 5a-d) and their novel air- and moisture-resistant pyridine (pyridine, 4 dimethylaminopyridine) containing palladium PEPPSI-type Pd(II) complexes (6a-e) were synthetized and characterized. The new palladium complexes have shown high activity in Mizoroki–Heck coupling reaction even at as low as 100 ppm loading (TON up to 10000). Kinetic studies revealed that reactions carried out in the presence of elemental mercury resulted in decrease in activity. It indicates that the coupling reaction may have both molecular and Pd(0)-mediated catalytic paths.


2017 ◽  
Vol 2017 ◽  
pp. 1-12 ◽  
Author(s):  
Radomir Jasiński ◽  
Oleg M. Demchuk ◽  
Dmytro Babyuk

The DFT calculations of the simplified model of the asymmetric Suzuki–Miyaura coupling reaction were performed at the M062x/LANL2DZ theory level at first. It was found that enantioselective reactions mediated by the palladium complexes of chiral C,P-ligands follow a four-stage mechanism similar to that proposed previously as one of the most credible mechanisms. It should be underlined that the presence of substituents in the substrates and the chiral ligand at ortho positions determines the energies of possible diastereoisomeric transition states and intermediates in initial reaction steps. This suggests that, in practice, a sharp selection of theoretically possible paths of chirality transfer from the catalyst to the product should have a place and, therefore, the absolute configuration of the formed atropisomeric product is defined and can be predicted.


2016 ◽  
Vol 70 (8) ◽  
Author(s):  
Shane C Van Wyk ◽  
Martin O. Onani ◽  
Ebbe Nordlander

AbstractSouth Africa is a mineral-rich country and one area in which minerals can be very important is catalysis. Over an extended period of time, homogeneous catalysis has grown to become very useful, particularly in the chemical and pharmaceutical industries. The organometallic compounds required in the catalysis industry have advanced from metallocenes to an alternative in the form of


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