Investigation of the catalytic activity of metal complexes fixed on a solid support. 10. Selective hydrogenation of allylbenzene in the presence of heterogeneous Pt-Sn-citrate complexes

1992 ◽  
Vol 41 (6) ◽  
pp. 1001-1003
Author(s):  
L. I. Gvinter ◽  
N. V. D'yakonova ◽  
T. P. Lutsko ◽  
V. Z. Sharf ◽  
P. G. Antonov
Keyword(s):  
Catalytic Activity ◽  
Metal Complexes ◽  
Selective Hydrogenation ◽  
Solid Support

Polymer-Bound 1-Aryl-3-alkyltriazenes as Modular Ligands for Catalysis. Part 2: Screening Immobilized Metal Complexes for Catalytic Activity

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

scholarly journals Metal Complexes of Schiff Bases of 3-Hydroxyquinoxaline-2-carboxaldehyde Encapsulated in Zeolite Y Cages: Potential Catalyst for Removing Phenol from Effluent Media

2021 ◽  
Vol 33 (11) ◽  
pp. 2746-2754
Author(s):  
N.R. Suja ◽  
T.K. Bindu Sharmila ◽  
S.R. Amrutha
Keyword(s):  
Catalytic Activity ◽  
Transition Metal ◽  
Metal Complexes ◽  
Schiff Bases ◽  
Transition Metal Complexes ◽  
Zeolite Y ◽  
Point Of View ◽  
Organic Transformations ◽  
Efficient Catalyst ◽  
Industrial Pollutants

Transition metal complexes are known to be efficient catalyst for many organic transformations. Encapsulation of metal complexes in zeolite cage brings many significant modifications in the structure of the metal complexes, which are very interesting from the catalytic point of view. This study aims in a comparative evaluation of the influence of structure of neat and encapsulated complexes in their catalytic activity. Phenol is one of the major industrial pollutants. Heterogenizing transition metal Schiff bases by encapsulation inside the zeolite would help to minimize the reuse problem of transition metal complexes. This article deals with the synthesis, characterization and catalytic activity studies of Co(II), Ni(II) and Cu(II) complexes of 3-hydroxyquinoxaline-2-carboxaldehyde with ethylenediamine (L1) and an o-phenylene diamine (L2).

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