Ruthenium(III) Schiff Base Complexes: Catalytic Activity in Aryl–Aryl Coupling Reaction and Antimicrobial Activity

2003 ◽  
Vol 33 (9) ◽  
pp. 1535-1553 ◽  
Author(s):  
C. Jayabalakrishnan ◽  
R. Karvembu ◽  
K. Natarajan
2019 ◽  
Vol 48 (42) ◽  
pp. 15942-15954
Author(s):  
Susheela Kumari ◽  
Bidisa Das ◽  
Saumi Ray

Encapsulation of palladium complex within the supercage of zeolite-Y moulds the guest complex such a way that it exhibits an exciting reactivity towards the Heck coupling by eliminating aggregation and tuning electron density of the metal.


Polyhedron ◽  
2016 ◽  
Vol 117 ◽  
pp. 90-96 ◽  
Author(s):  
Vladimír Kuchtanin ◽  
Lucia Kleščíková ◽  
Michal Šoral ◽  
Róbert Fischer ◽  
Zdeňka Růžičková ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (48) ◽  
pp. 38085-38092 ◽  
Author(s):  
Tahshina Begum ◽  
Manoj Mondal ◽  
Pradip K. Gogoi ◽  
Utpal Bora

A novel Pd@imine-SiO2 catalyst was prepared and found to exhibit excellent catalytic activity in a Suzuki-Miyaura cross-coupling reaction under aqueous media at room temperature.


2018 ◽  
Vol 80 (2) ◽  
Author(s):  
Shahrul Nizam Ahmad ◽  
Hadariah Bahron ◽  
Amalina Mohd Tajuddin ◽  
Syed Abdul Illah Alyahya Syed Abd Kadir

Coupling reaction between aryl halide and terminal alkyne in Sonogashira coupling reaction is important due to its extensive application in the resynthesis of natural products, production of drugs, dyes, and polymers. Efforts to increase rate of reaction has involved exploration of new catalysts. The current catalysts such as phosphine-based complexes are costly, air-sensitive and environmentally harmful. Nickel(II) Schiff base complexes were synthesized by reacting aromatic Schiff base ligands 2,2'-((1E,1'E)-(1,2-phenylenebis(azanylylidene))bis(metha-nylylidene))diphenol (L1H), 2,2'-((1E,1'E)-(1,2-phenylenebis(azanylylidene))bis(methanylylidene))bis(4-fluorophenol) (L1F), and 2,2'-((1E,1'E)-(1,2-phenylenebis(azanylylidene))bis-(methanylylidene))bis(4-methylphenol) (L1M) with nickel(II) acetate tetrahydrate to form NiL1H, NiL1F and NiL1M. The chemical structures were elucidated through physicochemical and spectral techniques namely elemental analysis, melting point, FTIR, 1H and 13C NMR, magnetic susceptibility and molar conductivity. All nickel(II) complexes were tested as catalysts in homogenous Sonogashira reaction between iodobenzene and phenylacetylene in DMSO for 12 hours at 140 oC. NiLF, a new nickel(II) complex, converted the highest percentage of iodobenzene (91%) while NiLH and NiLC converted 78% and 83% of iodobenzene, respectively. 


2016 ◽  
Vol 2 (3) ◽  
pp. 83-91 ◽  
Author(s):  
Laila H. Abdel-Rahman ◽  
Ahmed M. Abu-Dief ◽  
Rafat M. El-Khatib ◽  
Shimaa Mahdy Abdel-Fatah ◽  
Amin Abdou Seleem

2012 ◽  
Vol 51 (3) ◽  
pp. 1657-1674 ◽  
Author(s):  
Kusum K. Bania ◽  
Dipsikha Bharali ◽  
B. Viswanathan ◽  
Ramesh C. Deka

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