Archive for the ‘News’ Category

Converting methane into useful hydrocarbons

US scientists have demonstrated for the first time that a metal–carbon multiple bond complex can activate methane. The work could open the way for efficiently converting methane into useful hydrocarbons including ethylene, one of the fundamental building blocks of the chemical industry.

A transient titanium alkylidyne (the ring master) can cleanly tame methane (molecule inside cage)

Methane is the principal component of natural gas and a major contributor to global warming. It is therefore desirable to find cleaner and cheaper ways of using it as a resource by converting it into more useful chemicals. However, such reactions pose significant challenges because of methane’s low reactivity and strong tetrahedral C–H bonds, which are not readily accessible for chemical attack and activation.

The research could ultimately enable scientists to use methane as a feedstock for C–C bond formation, important for the production of chemicals including pharmaceuticals and plastics, say Daniel Mindiola (Indiana University) and colleagues.

Download Mindiola’s Edge article to find out more.

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Famous gold cluster structure revisited

Graphical abstract: A 58-electron superatom-complex model for the magic phosphine-protected gold clusters (Schmid-gold, Nanogold®) of 1.4-nm dimensionTeams from Germany, the US and Finland have re-investigated the structure of a famous gold-phosphine-halide compound.

The ‘‘Schmid Au55’’ cluster, originally formulated as Au55(PPh3)12Cl6, is one of the first and probably most utilised gold nanoparticles. However, the team found that the most energetically favourable anion is
[Au69(PR3)20Cl12]-1. It is energetically and chemically superior to the standard models based on Au55(PR3)12X6.

Download the Chemical Science Edge article to find out more.

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How polar are ionic liquids?

Ionic liquids interact with dissolved salts to give solutions that are completely different to salt solutions in traditional organic solvents or water, say UK scientists.

Ionic liquids are of great interest as green solvents but the way they solvate solutes isn’t well understood. Scientists studying their polarity have produced contradictory results – in some cases they are reported to be highly polar, in others non-polar.

Now Tom Welton and colleagues at Imperial College London say they’ve resolved this contradiction and have revealed a completely new solvent paradigm for salt solutions in ionic liquids.

In contrast to molecular solvents, where the solute cation and anion need to stay close to each other to preserve charge neutrality, ionic liquids solvate individual solute ions, explains Welton. This completely divorces the cations and anions from each other but the ionic liquid itself is capable of preserving the charge neutrality.

The polarity of ionic liquids depends on when you ask, adds Welton. Polarity measurements that record snapshots of the ionic liquid on a short timescale (such as measuring the position of the absorption maximum) ‘freeze out’ ionic movement and so the ionic liquid appears non-polar. Absorptivity measurements involve a longer timescale, allowing ion movement to dominate solvation, yielding a much higher polarity.

Read more in ‘Salts dissolved in salts‘ in Chemical Science.

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Superresolution imaging of membranes

Cell membranes are made up of a mixture of different lipids and proteins. Membrane lipids aren’t randomly distributed but instead form raft-like microdomains. These are thought to provide platforms for protein interaction allowing protein trafficking and cell signalling.

Scientists have found it difficult to study these microdomains because their reported size is smaller than the resolution of light microscopy. Now a team of scientists from Japan and Belgium have circumvented this limitation by designing probes for cholesterol and sphingolipid-enriched microdomains for use in superresolution microscopy.

Graphical abstract: Fluorescent probes for superresolution imaging of lipid domains on the plasma membraneThey visualised clustering of lipid molecules in nanodomains with a spatial resolution one order of magnitude better than the diffraction limit and were able to resolve the detailed structure of the domains.

Read more:
Fluorescent probes for superresolution imaging of lipid domains on the plasma membrane
Hideaki Mizuno, Mitsuhiro Abe, Peter Dedecker, Asami Makino, Susana Rocha, Yoshiko Ohno-Iwashita, Johan Hofkens, Toshihide Kobayashi and Atsushi Miyawaki, Chem. Sci., 2011, DOI: 10.1039/C1SC00169H

Johan Hofkens, one of the authors of this manuscript, is a plenary speaker at the forthcoming Challenges in Chemical Biology (ISACS5) meeting. Register by 24th June to hear him speak.

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Detecting ricin in liquid foods

A team of scientist from the US and India have developed a simple and sensitive way to detect ricin in liquid foods, such as orange juice and milk.

Graphical abstract: Aptamer-based surface-enhanced Raman scattering detection of ricin in liquid foodsRicin is a protein toxin naturally present in the castor bean plant (Ricinus communis); it is classified as a ‘select’ bioterror agent and was involved in a recent bioterrorism attack plot targeting US hotels and restaurants at multiple locations, as reported by the Department of Homeland Security officials in December 2010.

 Theodore Labuza, at the University of Minnesota, and colleagues developed a two-step assay, in which the ricin was first captured out of food matrices by aptamer-conjugated silver dendrites and then the Raman spectrum was directly read on the silver dendrites. The measurement is based on the Raman ‘‘finger-print’’ of the target itself. Combined with the specific capture agent, Labuza says false positive results are extremely unlikely.

The assay shows great promise as a rapid (<40min), sensitive, and simple ‘‘Yes/No’’ method to detect bio-weapons, say the researchers.

Find out more for free by downloading Labuza’s Chemical Science Edge article.

Also of interest
ChemComm Surface Enhanced Raman Spectroscopy web themed issue

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Challenges in Renewable Energy (ISACS4) – abstract submission deadline approaching

challenges in renewable energy (ISACS 4)

This exciting conference will review current research developments in renewable energy and highlight future challenges.

The recently released ISACS4 programme details a full schedule over the entire four days – take a look and discover those all important lecture titles from a series of outstanding plenary speakers.

Submit your poster abstract now – deadline 27 May 2011

Abstracts are invited for poster presentation within the themes of the conference:

  • Bioinspired systems
  • Battery technology
  • Electrochemistry
  • Photocatalysis
  • Solar harvesting
  • Energy storage

This is a fantastic opportunity to showcase your work – submit a poster before it’s too late!

Registration deadline 3 June 2011

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RSC Publishing hosts dinner in Japan

Hubert Girault, Chemical Science Associate Editor for analytical science, met up with RSC Publisher Niamh O’Connor and Hirofumi Seike (RSC Representative, Japan) in Kyoto on Sunday to host a dinner for leading physical and analytical chemists.

Clockwise from left: Hubert Girault, Richard van Duyne, Steven Soper, Richard Zare, Susan Zare, Niamh O'Connor, Hirofumi Seike

The group are in Japan for the IUPAC International Congress on Analytical Sciences 2011, which is on until 26th May.

Obviously there will be lots of discussion at the meeting about the best and latest advances in the analytical sciences. Here’s my pick of some of the most exciting recent Chemical Science articles in this area:

Heavy water hydration of mannose: the anomeric effect in solvation, laid bare
Nitzan Mayorkas, Svemir Rudić, Benjamin G. Davis and John P. Simons, Chem. Sci., 2011, 2, 1128-1134

Accelerated bimolecular reactions in microdroplets studied by desorption electrospray ionization mass spectrometry
Marion Girod, Encarnacion Moyano, Dahlia I. Campbell and R. Graham Cooks, Chem. Sci., 2011, 2, 501-510

Rapid prototyping of poly(dimethoxysiloxane) dot arrays by dip-pen nanolithography
Aaron Hernandez-Santana, Eleanore Irvine, Karen Faulds and Duncan Graham, Chem. Sci., 2011, 2, 211-215

These articles, like all Chemical Science content, are free to access until the end of this year. Sign up for the Chemical Science e-alert to get details of the exceptional content delivered straight to your inbox.

Hubert Girault is welcoming Chemical Science submissions in the areas of analytical science and electrochemistry. Submit to his editorial office today to be seen with the best.

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Challenges in Chemical Biology – one week until abstract submission deadline!

This exciting event will review current research developments and highlight future challenges in chemical biology.

The recently released ISACS5 programme details a full schedule over the entire four days – take a look and discover those all important lecture titles from a series of outstanding plenary speakers, including Nobel Laureates Thomas Steitz and Venki Ramakrishnan.

Submit your poster abstract now – deadline 27 May 2011

Abstracts are invited for poster presentation within the themes of the conference:
• The ribosome
• The origins of life
• Synthetic biology
• Engineered enzymes
• DNA nanotechnology
• Chemistry of surfaces
• Next generation pharmacology

This is a fantastic opportunity to showcase your work – submit a poster before it’s too late!

Registration – early bird deadline 27 May 2011

Make sure you are part of this unique conference experience! To guarantee your place whilst making a great saving through our early bird discount, register online today.

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Studying reaction mechanisms in the solid state

Photochemical reactions in crystals can show excellent selectivity, thanks to the rigid environment. But the development and applications of reactions in crystals has suffered due to a lack of mechanistic insight.

Now Miguel Garcia-Garibay, at the University of California, Los Angeles, US, and colleagues have published the first report addressing the absolute reaction kinetics of a reaction taking place in the crystalline solid state, using conventional pump-probe methods with excitation in the nanosecond and femtosecond time domains.

Graphical abstract: Steady state and transient kinetics in crystalline solids: the photochemistry of nanocrystalline 1,1,3-triphenyl-3-hydroxy-2-indanone

They studied the Norrish type I decarbonylation of a 2-indanone in solution and as a nanocrystalline suspension and, for the first time, detected the radical intermediates involved in the reaction.

To find out more, download the group’s Chemical Science Edge article for free.

Thinking of submitting an article yourself? No colour charges, no page charges or limits, and free access* providing wide visibility – make Chemical Science your number one choice for your very best research.

* until the end of 2011

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Enantioselective synthesis of cyclic carbamimidates

A racemic Au(I)-catalysed three-component reaction has been developed by US scientists to prepare cyclic carbamimidates from imines, terminal alkynes and sulfonylisocyanates. This reaction exploits the carbophilic π-acidity of gold catalysts to first activate an alkyne toward deprotonation and then to activate the internal alkyne generated toward intramolecular O-cyclisation.

Unlike similar previously reported multicomponent gold-catalysed reactions, the stereocentre generated during the alkynylation is preserved in the product. This trait was exploited by developing an enantioselective variant, using an unusual trans-1-diphenylphosphino-2-arylsulfamidocyclohexane ligand.

Graphical abstract: Enantioselective synthesis of cyclic carbamimidates via a three-component reaction of imines, terminal alkynes, and p-toluenesulfonylisocyanate using a monophosphine gold(i) catalyst

Moderate to excellent levels of enantioselectivity were obtained using a variety of N-arylbenzylidene anilines.

Find out more:
M J Campbell and F D Toste, Chem. Sci., 2011, DOI: 10.1039/c1sc00160d

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