Catalytic activity of metal complexes fixed on a solid carrier. I. Palladium complexes deposited on ionites in hydrogenation reactions

Author(s):  
V. Z. Sharf ◽  
V. D. Kopylova ◽  
L. P. Karapetyan ◽  
E. L. Frumkina ◽  
L. Kh. Freidlin ◽  
...  
2016 ◽  
Vol 71 (6) ◽  
pp. 667-676 ◽  
Author(s):  
Eduard Rais ◽  
Ulrich Flörke ◽  
René Wilhelm

AbstractThe presented work describes the synthesis of new six- and seven-membered haloamidinium salts and their reaction with different metals. The isolated metal complexes were tested in a catalytic reaction. Two different synthetic routes were applied to prepare five different salts. Chloroamidinium salts were very water-sensitive in comparison to their corresponding bromoamidinium salts. Hence, the preparation of the less sensitive bromoamidinium salts was higher prioritized. The formed salts were converted with metal sources to N-heterocyclic carbene (NHC) metal complexes through an oxidative insertion into the C–X bond. This type of formation is less examined for the synthesis of extended NHC metal complexes. Pd(PPh3)4 and cobalt powder were applied as metal sources, whereby two palladium complexes were isolated, characterized, and their crystal and molecular structures determined. The palladium complexes were investigated in the Suzuki-Miyaura reaction and showed promising catalytic activity.


Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 656
Author(s):  
Henrietta Kovács ◽  
Krisztina Orosz ◽  
Gábor Papp ◽  
Ferenc Joó ◽  
Henrietta Horváth

Na2[Ir(cod)(emim)(mtppts)] (1) with high catalytic activity in various organic- and aqueous-phase hydrogenation reactions was immobilized on several types of commercially available ion-exchange supports. The resulting heterogeneous catalyst was investigated in batch reactions and in an H-Cube flow reactor in the hydrogenation of phenylacetylene, diphenylacetylene, 1-hexyne, and benzylideneacetone. Under proper conditions, the catalyst was highly selective in the hydrogenation of alkynes to alkenes, and demonstrated excellent selectivity in C=C over C=O hydrogenation; furthermore, it displayed remarkable stability. Activity of 1 in hydrogenation of levulinic acid to γ-valerolactone was also assessed.


2016 ◽  
Vol 818 ◽  
pp. 179-184 ◽  
Author(s):  
Liangru Yang ◽  
Xinchi Zhang ◽  
Jinwei Yuan ◽  
Yongmei Xiao ◽  
Pu Mao

2002 ◽  
Vol 12 (14) ◽  
pp. 1849-1851 ◽  
Author(s):  
Stefan Bräse ◽  
Stefan Dahmen ◽  
Frank Lauterwasser ◽  
Nicholas E. Leadbeater ◽  
Emma L. Sharp

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