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Graphene Supports for Catalytic Reduction

C2RA20400BGraphene is one of the most exciting and promising materials to have emerged into the laboratory in recent years. Among its many possibilities it can be used as a support for various catalysts, such as the highly-dispersed ultrafine platinum nanoparticles synthesised by Baoqiang Sheng and colleagues at Key Laboratory of Organic Synthesis of Jiangsu Province in China.

The group used their graphene-supported platinum catalysts to reduce various unsaturated compounds, including not only C-C double and triple bonds but also nitroarenes. These could be selectively converted to their corresponding functionalized anilines – important intermediates in the preparation of polymers, urethanes, dyes, pharmaceuticals, and other industrially-important chemical products.

They claim  excellent yields (over 99% in most cases) under mild conditions, with the ability to accelerate the reaction rate by increasing the pressure to 4 atm, giving complete hydrogenation products in ten minutes.

The paper provides details of the preparation and characterisation of the supported catalysts, and lists the experimental procedures together with results of the reductions that were carried out.

This article is currently free to access through the RSC Advances website:

Highly-dispersed ultrafine Pt nanoparticles on graphene as effective hydrogenation catalysts, Baoqiang Sheng, Lei Hu, Tingting Yu, Xueqin Cao and Hongwei Gu, RSC Adv., 2012, 2, 5520–5523

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Organometallics in catalysis: an article collection

Perhaps the most well-known applications of organometallics in catalysis are the Ziegler–Natta catalysts which are used to generate polymers, the catalysts are made up of mixtures of transition metal halides and organo-aluminium complexes. Karl Ziegler and Giulio Natta were awarded the 1963 Nobel Prize in Chemistry for their discovery and development of the catalysts, which today are the most commonly used for the manufacture of polythene.

The esteemed history of organometallics are not to be under-estimated and include Grignard’s reagents, the Heck reaction, Schrock catalysts, Grubbs’ catalysts and the Suzuki Coupling to name just a few. Organometallic compounds have revolutionised science and industry and to keep you up to date with the latest break-through research being made across all areas of organometallics in catalysis, we have made this cross-journal article collection free until the 26th September.

Click here for the full list of free articles

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Extraction of uranium from seawater with ionic liquids

A team from Alabama, USA have reported a highly selective extraction of the uranyl ion from aqueous solution via η2  coordination using hydrophobic amidoxime-functionalized ionic liquids.

Graphical abstract: Highly selective extraction of the uranyl ion with hydrophobic amidoxime-functionalized ionic liquids via η2 coordinationThe world’s oceans contain approximately one thousand times the terrestrial supply of uranium, but a selective, cheap and insoluble extractant must be developed to overcome the energetic and economic challenge of the low concentrations in seawater and the variety of interfering ions.  In the 1980s, after studying over 200 adsorbents, it was reported that the amidoxime functional group, RC(NH2)(=NOH), appended to polyacrylonitrile was highly selective towards uranium.

Though well-studied, the coordination of amidoxime to the uranyl ion is not well understood. In this paper, Robin Rogers and his team from the University of Alabama have been able to utilize the functionality of ionic liquids to demonstrate the controversial coordination mechanism for extraction of uranium from seawater by amidoxime extractants.  They have demonstrated, through extraction, spectroscopic, and crystallographic studies that hydrophobic, amidoxime-functionalized ionic liquids selectively extract the uranyl ion from aqueous solution via η2 coordination. 

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Highly selective extraction of the uranyl ion with hydrophobic amidoxime-functionalized ionic liquids via η2 coordination
Patrick S. Barber ,  Steven P. Kelley and Robin D. Rogers
RSC Adv., 2012, Advance Article
DOI: 10.1039/C2RA21344C

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