نتایج جستجو برای: iron catalysts

تعداد نتایج: 173649  

2016
Margaret Yankey James Darkwa

Five new iron(III) 1-hexene polymerisation catalysts were prepared from the reactions of 2,4-di-tert-butyl-6-(2-(1H-imidazol-4-yl)ethylimino)methylphenol (L1), or 4-tert-butyl-6-(2-(1Himidazol-4-yl)ethylimino)methylphenol (L2) or 2,4-di-tert-butyl-6-[(2-pyridin-2-yl-ethylimino)methyl-phenol (L3) with anhydrous iron(II) halides to form [FeCl2(L1)] (1), [FeBr2(L1)] (2), [FeI2(L1)] (3), [FeBr2(L2)...

Journal: :Dalton transactions 2014
Peter E Sues Karl Z Demmans Robert H Morris

The asymmetric reduction of ketones and imines by transfer of hydrogen from isopropanol as the solvent catalyzed by metal complexes is a very useful method for preparing valuable enantioenriched alcohols and amines. Described here is the development of three generations of progressively more active iron catalysts for this transformation. Key features of this process of discovery involved the re...

2011
Saveria Santangelo Elpida Piperopoulos Maurizio Lanza Giuliana Faggio Giacomo Messina Candida Milone

The synthesis of carbon nanotubes (CNTs) by chemical vapor deposition (CVD) of isobutane (i‐C4H10) over sodium‐exchanged K10‐montmorillonite based iron‐ catalysts is investigated. By studying the influence of iron‐addition (5–25 wt%) on the catalyst performances, at 700 °C, an empirical relationship is derived relating the mass of CNTs synthesized with the exposed ...

Journal: :Chemical communications 2014
Peter Comba Yong-Min Lee Wonwoo Nam Arkadius Waleska

Organic substrates (specifically cis-1,2-dimethylcyclohexane, DMCH) are oxidized by O2 in the presence of iron(II)-bispidine complexes. It is shown that this oxidation reaction is not based on O2 activation by the nonheme iron catalysts as in Nature but due to a radical-based initiation, followed by a radical- and ferryl-based catalytic reaction.

Journal: :Chemical communications 2015
Xiangping Zhou Jian Ji Di Wang Xuezhi Duan Gang Qian De Chen Xinggui Zhou

Hierarchical structured α-Al2O3 is shown to be able to effectively disperse and immobilize iron species, in comparison with commercial α-Al2O3. After promotion using an appropriate amount of sulfur, iron catalysts exhibit not only enhanced Fischer-Tropsch synthesis activity and selectivity toward lower olefins, but also increased resistance against carbon deposits.

Journal: Nanochemistry Research 2018

As a novel performance, methanol gas conversion to dimethoxymethane (DMM) in one-step based on Fe-Mo-O (iron molybdate mixed oxides) catalysts with high surface area fabricated by metal organic frameworks (MOFs) precursors was improved. For this approach, at first, Fe(III) precursors (iron (III) 1,3,5-benzenetricarboxylate (MIL-100 (Fe) and iron terephthalate (MOF-...

Journal: :Angewandte Chemie 2008
Chandra M Rao Volla Pierre Vogel

Carbon–carbon cross-coupling reactions are very important in the areas of material science and medicinal chemistry. Most current methods require expensive transition-metal catalysts (for example, based on Cu, Pd, Co, Ni, Pt, Ru, and Rh) and ligands (for example, phosphines). Early reports by Kharasch and Reinmuth in 1954 and then by Tamura and Kochi in 1971 suggested that inexpensive Grignard r...

2014
Carolina Solis Maldonado Javier Rivera De la Rosa Carlos J. Lucio-Ortiz Aracely Hernández-Ramírez Felipe F. Castillón Barraza Jaime S. Valente

The role of iron in two modes of integration into alumina catalysts was studied at 0.39 wt% Fe and tested in trichloroethylene combustion. One modified alumina was synthesized using the sol-gel method with Fe added in situ during hydrolysis; another modification was performed using calcined alumina, prepared using the sol-gel method and impregnated with Fe. Several characterization techniques w...

Journal: :Chemical communications 2011
Rajenahally V Jagadeesh Gerrit Wienhöfer Felix A Westerhaus Annette-Enrica Surkus Marga-Martina Pohl Henrik Junge Kathrin Junge Matthias Beller

Pyrolysis of iron-phenanthroline complexes supported on carbon leads to highly selective catalysts for the reduction of structurally diverse nitroarenes to anilines in 90-99% yields. Excellent chemoselectivity for the nitro group reduction is demonstrated.

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