Palladium nanoparticles immobilized on a magnetic chitosan-anchored Schiff base: applications in Suzuki–Miyaura and Heck–Mizoroki coupling reactions

2017 ◽  
Vol 41 (13) ◽  
pp. 5595-5604 ◽  
Author(s):  
Anuradha Anuradha ◽  
Shweta Kumari ◽  
Samaresh Layek ◽  
Devendra D. Pathak
Keyword(s):  
Schiff Base ◽  
Palladium Nanoparticles ◽  
Coupling Reactions ◽  
Magnetic Chitosan ◽  
Ft Ir

A palladium nanocatalyst Fe3O4@CS-SB-Pd has been synthesized and characterized by FT-IR, XRD, XPS, FESEM, EDX, TEM, TGA, and ICP-AES analysis.

Malus domestica Mediated Synthesis of Palladium Nanoparticles and Investigation of Their Catalytic Activity Towards the Suzuki Coupling Reactions

2018 ◽  
Vol 10 (3) ◽  
pp. 373-377 ◽  
Author(s):  
Farah Qazi ◽  
Zakir Hussain ◽  
Soneela Asghar ◽  
Ghayoor Abbas ◽  
Muhammad Riaz
Keyword(s):  
Gas Chromatography ◽  
Catalytic Activity ◽  
Malus Domestica ◽  
Palladium Nanoparticles ◽  
Suzuki Coupling ◽  
Coupling Reactions ◽  
X Rays ◽  
Fruit Extract ◽  
Vis Spectroscopy ◽  
Ft Ir

Synthesis of nanoparticles through green methods is considered to be more eco-friendly and facile as compared to conventional physical and chemical methods. In this work, an environmental friendly method to synthesize palladium nanoparticles (Pd-NPs) by using a fruit extract has been reported. This extract obtained from Malus domestica (apple); acted as a source of reducing agent and functioned as a capping agent as well. The Pd-NPs were monitored and characterized by ultraviolet-visible (UV-Vis) spectroscopy; powder X-rays diffraction (XRD), scanning electron microscopy (SEM) and Fourier-transform infra-red (FT-IR) spectroscopy. FT-IR spectra revealed the presence of abundant amounts of ascorbic acid in the fruit extract which is assumed to reduce the Palladium chloride to Pd-NPs. XRD results confirmed the crystalline nature of Pd-NPs (JCPDS: No. 05-0681, space group: Fm3m (225)). These nanoparticles were further investigated for their catalytic activity towards the Suzuki coupling reactions where by employing only 2 mol% of the catalyst loading these Pd-NPs demonstrated excellent catalytic activity. Progress and completion of reactions were monitored by gas chromatography (GC) while products formed were characterized by gas chromatography-mass spectrometry (GC-MS), FT-IR as well as from their melting points data. Pd-NPs showed excellent catalytic activity; thereby suggesting their potential and scope for various other catalytic transformations.

Chiral Mn(III) Salen Complex Immobilized on CuFe2O4@SiO2-NH2 NPs: A Cheap and Efficient Catalyst for N-arylation of Aryl Halides and Phenylboronic Acid Under Mild Conditions

2020 ◽  
Vol 17 (11) ◽  
pp. 857-863
Author(s):  
Mohammad Ali Nasseri ◽  
Seyyedeh Ameneh Alavi ◽  
Milad Kazemnejadi ◽  
Ali Allahresani
Keyword(s):  
Phenylboronic Acid ◽  
Significant Loss ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Efficient Catalyst ◽  
Aryl Chlorides ◽  
Mild Conditions ◽  
Cross Coupling Reactions ◽  
Salen Complex ◽  
Ft Ir

A convenient and efficient chiral CuFe2O4@SiO2-Mn(III) Ch.salen nanocatalyst has been developed for the C-N cross-coupling reactions of aryl halides/ phenylboronic acid with N-heterocyclic compounds in water and/or DMSO under mild conditions. The catalyst could be applied for the N-arylation of a variety of nitrogen-containing heterocycles with aryl chlorides, bromides, iodides and phenylboronic acid under mild conditions. Moderate to good yields were achieved for all substrates. The structure of catalyst was characterized using various techniques including FT-IR, FE-SEM, EDX, XRD, TEM and TGA. The catalyst can be simply recovered and reused for several times without significant loss of activity.

scholarly journals Synthesis and Structural Characterization of (E)-4-[(2-Hydroxy-3-methoxybenzylidene)amino]butanoic Acid and Its Novel Cu(II) Complex

Molbank ◽  
10.3390/m1179 ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. M1179
Author(s):  
Eleftherios Halevas ◽  
Antonios Hatzidimitriou ◽  
Barbara Mavroidi ◽  
Marina Sagnou ◽  
Maria Pelecanou ◽  
...  
Keyword(s):  
Schiff Base ◽  
Gamma Aminobutyric Acid ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Polymeric Compound ◽  
Bridging Ligands ◽  
1H And 13C Nmr ◽  
One Dimensional ◽  
Ft Ir

A novel Cu(II) complex based on the Schiff base obtained by the condensation of ortho-vanillin with gamma-aminobutyric acid was synthesized. The compounds are physico-chemically characterized by elemental analysis, HR-ESI-MS, FT-IR, and UV-Vis. The complex and the Schiff base ligand are further structurally identified by single crystal X-ray diffraction and 1H and 13C-NMR, respectively. The results suggest that the Schiff base are synthesized in excellent yield under mild reaction conditions in the presence of glacial acetic acid and the crystal structure of its Cu(II) complex reflects an one-dimensional polymeric compound. The molecular structure of the complex consists of a Cu(II) ion bound to two singly deprotonated Schiff base bridging ligands that form a CuN2O4 chelation environment, and a coordination sphere with a disordered octahedral geometry.

Organostannoxane-Supported Palladium Nanoparticles. Highly Efficient Catalysts for Suzuki-Coupling Reactions

2009 ◽  
Vol 28 (20) ◽  
pp. 5883-5888 ◽  
Author(s):  
Vadapalli Chandrasekhar ◽  
Ramakirushnan Suriya Narayanan ◽  
Pakkirisamy Thilagar
Keyword(s):  
Palladium Nanoparticles ◽  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Highly Efficient ◽  
Supported Palladium

Suzuki coupling reactions catalyzed by Schiff base supported palladium complexes bearing the vitamin B6 cofactor

2021 ◽  
Vol 505 ◽  
pp. 111528
Author(s):  
Abdollah Neshat ◽  
Mohammad Gholinejad ◽  
Hafize Özcan ◽  
Faezeh Khosravi ◽  
Ali Mousavizadeh Mobarakeh ◽  
...  
Keyword(s):  
Schiff Base ◽  
Vitamin B6 ◽  
Suzuki Coupling ◽  
Palladium Complexes ◽  
Coupling Reactions ◽  
Supported Palladium

Synthesis,Characterization and Evaluation of Biological Activity of Sulfonylhydrazide-Schiff Base" (E)- N’-(2,5-dimethoxybenzalidene) naphthalene-2-sulfonohydrazide"

2020 ◽  
Vol 8 (1) ◽  
pp. 01-11
Author(s):  
Sameer Amereih ◽  
Abd Daraghmeh ◽  
Ismail Warad ◽  
Mohammed Al-Nuri
Keyword(s):  
Schiff Base ◽  
Inhibitory Concentration ◽  
Condensation Reaction ◽  
Gram Negative Bacteria ◽  
Biological Applications ◽  
Bacteriostatic Effect ◽  
1H And 13C Nmr ◽  
13C Nmr Analysis ◽  
Ft Ir

Condensation reaction of naphthalene -2-Sulfonylhydrazide, as starting material with 2,5-dimethoxy benzaldehyde was used to produce (E)-N’-(2,5-dimethoxybenzalidene)naphthalene-2-sulfonohydrazide. The Schiff base product was isolated, purified and then spectrally characterized via UV-Vis, GC/MS, FT-IR, 1H and 13C NMR analysis, where strong evidences confirmed the formation of the desired product. Antimicrobial activity of Schiff base product was evaluated in vitro against several types of bacteria such as: Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae and MRSA by Minimum Inhibitory Concentration (MIC) test using tetracycline (TE) as a standard antibiotic. The tests showed a promising bacteriostatic effect of this compound against gram negative bacteria such as P. aeruginosa and K. pneumoniae, such character is valuable for biological applications.

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