Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
Authors
Keywords
-
Journal
NEW JOURNAL OF CHEMISTRY
Volume 42, Issue 3, Pages 1757-1761
Publisher
Royal Society of Chemistry (RSC)
Online
2017-12-13
DOI
10.1039/c7nj02513k
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Green synthesis of palladium nanoparticles mediated by black tea leaves ( Camellia sinensis ) extract: Catalytic activity in the reduction of 4-nitrophenol and Suzuki-Miyaura coupling reaction under ligand-free conditions
- (2017) Sadaf Lebaschi et al. JOURNAL OF COLLOID AND INTERFACE SCIENCE
- Preparation of core/shell nanostructure Fe 3 O 4 @PEG400-SO 3 H as heterogeneous and magnetically recyclable nanocatalyst for one-pot synthesis of substituted pyrroles by Paal-Knorr reaction at room temperature
- (2017) Fahimeh Bonyasi et al. JOURNAL OF COLLOID AND INTERFACE SCIENCE
- Immobilization of palladium nanoparticles on ionic liquid-triethylammonium chloride functionalized magnetic nanoparticles: As a magnetically separable, stable and recyclable catalyst for Suzuki-Miyaura cross-coupling reactions
- (2017) Hojat Veisi et al. TETRAHEDRON LETTERS
- Biguanidine-functionalized chitosan to immobilize palladium nanoparticles as a novel, efficient and recyclable heterogeneous nanocatalyst for Suzuki-Miyaura coupling reactions
- (2016) Hojat Veisi et al. APPLIED ORGANOMETALLIC CHEMISTRY
- Synthesis and characterization of insoluble cobalt(II), nickel(II), zinc(II) and palladium(II) Schiff base complexes: Heterogeneous catalysts for oxidation of sulfides with hydrogen peroxide
- (2016) Saeid Menati et al. COMPTES RENDUS CHIMIE
- Preparation of polydopamine sulfamic acid-functionalized magnetic Fe3O4 nanoparticles with a core/shell nanostructure as heterogeneous and recyclable nanocatalysts for the acetylation of alcohols, phenols, amines and thiols under solvent-free conditions
- (2016) Hojat Veisi et al. GREEN CHEMISTRY
- Palladium stabilized by 3,4-dihydroxypyridine-functionalized magnetic Fe3O4 nanoparticles as a reusable and efficient heterogeneous catalyst for Suzuki reactions
- (2016) Mozhgan pirhayati et al. RSC Advances
- A highly stable and efficient magnetically recoverable and reusable Pd nanocatalyst in aqueous media heterogeneously catalysed Suzuki C-C cross-coupling reactions
- (2015) Bahareh Abbas Khakiani et al. APPLIED ORGANOMETALLIC CHEMISTRY
- Selective oxidation of sulfides to sulfoxides using hydrogen peroxide over Au/CTN–silica catalyst
- (2015) Fang Wang et al. CATALYSIS COMMUNICATIONS
- Application of 1,4-bis(3-methylimidazolium-1-yl)butane ditribromide [bMImB]·(Br3)2 ionic liquid reagent for selective oxidation of sulfides to sulfoxides
- (2015) Abbas Amini Manesh et al. RSC Advances
- Chemoselective hydration of nitriles to amides using hydrated ionic liquid (IL) tetrabutylammonium hydroxide (TBAH) as a green catalyst
- (2015) Hojat Veisi et al. RSC Advances
- Green and effective route for the synthesis of monodispersed palladium nanoparticles using herbal tea extract (Stachys lavandulifolia) as reductant, stabilizer and capping agent, and their application as homogeneous and reusable catalyst in Suzuki couplin
- (2014) Hojat Veisi et al. APPLIED ORGANOMETALLIC CHEMISTRY
- Sulfamic acid heterogenized on functionalized magnetic Fe3O4nanoparticles with diaminoglyoxime as a green, efficient and reusable catalyst for one-pot synthesis of substituted pyrroles in aqueous phase
- (2014) Hojat Veisi et al. APPLIED ORGANOMETALLIC CHEMISTRY
- Functionalization of fullerene (C60) with metformine to immobilized palladium as a novel heterogeneous and reusable nanocatalyst in the Suzuki–Miyaura coupling reaction at room temperature
- (2014) Hojat Veisi et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Copper–Schiff base complex catalyzed oxidation of sulfides with hydrogen peroxide
- (2014) Prasanta Gogoi et al. TETRAHEDRON LETTERS
- Selective synthesis of sulfoxides and sulfones from sulfides using silica bromide as the heterogeneous promoter and hydrogen peroxide as the terminal oxidant
- (2014) Behrooz Maleki et al. RSC Advances
- DABCO tribromide immobilized on magnetic nanoparticle as a recyclable catalyst for the chemoselective oxidation of sulfide using H2O2 under metal- and solvent-free conditions
- (2013) Amin Rostami et al. CATALYSIS COMMUNICATIONS
- Synthesis of biguanide-functionalized single-walled carbon nanotubes (SWCNTs) hybrid materials to immobilized palladium as new recyclable heterogeneous nanocatalyst for Suzuki–Miyaura coupling reaction
- (2013) Hojat Veisi et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Synthesis and characterization of dl-thioctic acid (DLTA)–Fe3O4 nanocomposite
- (2011) E. Karaoğlu et al. JOURNAL OF ALLOYS AND COMPOUNDS
- Palladium nanoparticle supported on cobalt ferrite: An efficient magnetically separable catalyst for ligand free Suzuki coupling
- (2011) Kula Kamal Senapati et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Poly(N,N′-dichloro-N-ethylbenzene-1,3-disulfonamide) and N,N,N′,N′-Tetrachlorobenzene-1,3-disulfonamide as Novel Reagents for the Synthesis of N-Chloroamines, Nitriles and Aldehydes
- (2009) Ramin Ghorbani-Vaghei et al. SYNTHESIS-STUTTGART
- Poly(N,N′-dibromo-N-ethyl-benzene-1,3-disulfonamide), N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide and novel poly(N,N′-dibromo-N-phenylbenzene-1,3-disulfonamide) as powerful reagents for benzylic bromination
- (2009) Ramin Ghorbani-Vaghei et al. TETRAHEDRON LETTERS
- Selective synthesis of sulfoxides and sulfones by tantalum(V) catalyzed oxidation of sulfides with 30% hydrogen peroxide
- (2008) Masayuki Kirihara et al. TETRAHEDRON LETTERS
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started