Nanoscale spectroscopy with optical antennas

Optical antennas made of gold nanoparticles can enhance the sensitivity of photoluminescence and vibrational spectroscopy, according to research recently published in Chemical Science.

In traditional microscopy and spectroscopy, components such as lenses, mirrors and diffractive elements are used to control and focus the optical radiation. This relies on the wave nature of the radiation and means the smallest volume to which the radiation can be localised, and so the technique’s sensitivity, is limited by diffraction.

Now Lukas Novotny and colleagues at the University of Rochester, USA, have taken inspiration from radio wave manipulation and designed an optical antenna that can boost the interaction between light and the particle being studied. The fluorescence of a single molecule can be enhanced by more than a factor of 10 using this technique. The optical antenna, which consists of a single colloidal gold nanoparticle on the end of a pointed dielectric fibre, replaces a conventional focusing lens or objective, so the incoming light can be focused to dimensions smaller than the diffraction limit.

As well as improving chemical and biological sensing, the technique holds promise for resolving open questions in surface enhanced Raman scattering and fluorescence, says Novotny.

Read the Edge article to find out more. And to put the focus on your own exciting research, submit today to Chemical Science.

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C–H functionalisation at room temperature

UK chemists have moved a step closer to conquering a significant synthetic challenge by developing a C–H bond functionalisation reaction that can generate a diversity of molecular frameworks at room temperature.

A broad range of C–H transformations can be catalysed by a variety of transition metals at high temperatures. But Matthew Gaunt’s group at the University of Cambridge aims to develop a synthetic toolbox comprising mild metal-catalysed C–H functionalisation reactions to make it easier to make complex molecules.

They investigated the reactions of β-arylethylamine, a motif commonly found in medicines and natural products. Attempts to catalytically transform the phenylalanine ethyl ester had previously failed but when the group introduced an aryl group onto the amine system, they were able to carbonylate, arylate and aminate the C–H bond. The reaction works on a variety of substrates and is tolerant of stereogenic centres and complex functionality.

Graphical abstract: Amine directed Pd(ii)-catalyzed C–H bond functionalization under ambient conditions

Find out more in Dr Gaunt’s Edge article, now online and free to access.

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Cobalt-gadolinium cages as magnetic refrigerants

A new family of cobalt-gadolinium cage compounds are highly efficient for low temperature cooling, say European scientists.

Liquid helium is currently used to achieve very low temperatures in a large amount of technology, such as super-conducting magnets that are needed for magnetic resonance imaging scanners. But the world supply of helium is falling, making it more expensive. An alternative method for low temperature cooling is to use demagnetisation of magnetic materials.

Now Richard Winpenny at the University of Manchester and colleagues have synthesised a new family of cobalt-gadolinium cage compounds, creating heterometallic molecular squares that show potential for the creation of magnetic coolants. Winpenny explains that magnetic coolants work because demagnetisation increases the entropy of the material, and this increase in entropy comes from taking heat out of the surroundings.

Cobalt-gadolinium molecular squares
Cobalt-gadolinium molecular squares act as super coolants

 

 

Juergen Schnack at the University of Bielefeld, Germany, an expert in the area of magnetic molecules, comments: ‘most interesting for me is the ability to synthesise such structures in such a great variety as demonstrated by the different grids of this work. This justifies our hopes that compounds with desired properties, for instance a large magnetocaloric effect – where compounds show a large change in temperature with a change in the magnetic field – are achievable.’

The highly anisotropic cobalt(II) ions in these compounds would be expected to have an adverse effect on the magnetocaloric effect, according to the scientists, but anti-ferromagnetic exchange between the octahedral cobalt ions appears to cancel out their contribution.

‘We have a fairly precise understanding of what is needed for a good magnetic coolant,’ says Winpenny. ‘What is surprising is that cobalt(II) complexes shouldn’t meet those requirements, and yet the complexes we’ve studied look interesting. Therefore I think we are going to find a few more surprises along the way and maybe we will need better theory as we proceed.’

Rachel Cooper

To find out more about this ‘cool’ research, download the Chemical Science Edge article for FREE.

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Chemical Science issue 5 now online!

From total synthesis to carbon nanotubes to molecular magnets – Chemical Science has it covered

Read all the exceptional content in the latest issue for free online including:

Splitting methanol: the first clear evidence of photocatalysed methanol splitting on titanium dioxide helps to explain why hydrogen production is more efficient for methanol–water mixtures than water alone

Biogenetically inspired approach to alkaloid family: the synthesis of an entire family of marine alkaloids that show potent anticancer activity and potential for treating Alzheimer’s disease

One for all, all for one!: A single chiral auxiliary and synthetic route can be used for a three-step preparation of enantiopure β3h, β2h and β2,3-amino acids

The issue also includes a Perspective on antifreeze glycoproteins and a Mini review on imaging molecular ions.

If you have some exciting results to report, submit to Chemical Science today and be seen with the best.

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Molecular bowl binds fullerene

US chemists have made a new type of molecular bowl that binds strongly to C70 fullerenes.

molecular bowl

hexabenzocoronene

Colin Nuckolls, at Columbia University, New York, and colleagues joined together the proximal carbons of contorted hexabenzocoronenes using solution-based, palladium-catalysed chemistry. The resulting shallow bowl-shaped molecules bind C70 very strongly and are also better than their hexabenzocoronene precursors at stabilising negative charge.

The unique optical, electronic and structural properties of these new bowl-shaped polycyclic aromatic hydrocarbons provide opportunities to create new organic materials, novel host-guest complexes and improved photovoltaics, says Nuckolls.
Bowled over by this research? Read the Edge article and tell us what you think below.

Recognition starts here – submit your exceptional research to Chemical Science today.

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Exploring magnetisation behaviour in frozen solutions

If you thought squid only belonged in the depths of the ocean, think again. SQUID, or superconducting quantum interference device, has been used to study single-molecule magnets (SMMs) in solution, which could help us store more information on hard drives in future.

As the demand for increased information storage continues to rise, scientists have turned to the development of new nanostructured materials, incorporating SMMs. These tiny magnets can store information depending on the charge and spin properties of their electrons. But until now, there have been few studies to examine how much of these molecules’ magnetic properties come from their molecular properties and how much comes from the way they are packed together in the solid-state. Graphical abstract: Frozen-solution magnetisation dynamics of hexanuclear oxime-based MnIII Single-Molecule Magnets

Using SQUID, which is a very sensitive device for detecting weak magnetic fields, Euan Brechin and colleagues have studied the spin properties of frozen solutions of two different hexanuclear manganese (Mn6) complexes. The two compounds display different spin-relaxation properties in the solid-state, but similar spin-dynamics once in solution. Brechin believes the study demonstrates that the SMM behaviour is intrinsically a molecular effect that can be modulated in the solid-state by crystal packing strain effects.

Read the full story in the Chemical Science Edge article, which, like all Chemical Science articles, is free to download until the end of 2011.

Be seen with the best – submit to Chemical Science today.

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Dissecting tunicamycin biosynthesis

40 years after it was first isolated, UK scientists have identified the biosynthetic genes of an important antibiotic, offering insights into its poorly understood biosynthetic pathway.

Tunicamycin antibiotics have attracted much attention (over 8000 citations) due to their unusual structure and potent inhibition of bacterial cell wall biosynthesis. Although they have been chemically synthesised, the lack of a sequence for the tunicamycin gene cluster (or any part of it) has left scientists puzzled over its biosynthetic pathway.

Now Benjamin Davis, at the University of Oxford, and colleagues have identified the tunicamycin biosynthesis genes in Streptomyces chartreusis, a soil bacterium, using genome sequencing and mining. Using this genetic insight, they have proposed the detailed biosynthetic pathway to this family of antibiotics.

Graphical abstract: Dissecting tunicamycin biosynthesis by genome mining: cloning and heterologous expression of a minimal gene cluster

The studies unlock a comprehensive and unusual toolbox of biosynthetic machinery with which to create variants of this natural product, says Davis. He anticipates this will lead to future therapeutic antibiotics with improved antibacterial activity and reduced cytotoxicity.

Find out more in Davis’ Chemical Science Edge article, downloadable for free. Access our free content any time, any place by registering for an RSC Publishing personal account today.

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Top ten most accessed articles in August

This month sees the following articles in Chemical Science that are in the top ten most accessed:-

Asymmetric Bronsted acid catalysis in aqueous solution 
Magnus Rueping and Thomas Theissmann 
Chem. Sci., 2010, 1, 473 – 476, DOI: 10.1039/c0sc00206b 

Oxygen reduction reactivity of cobalt(ii) hangman porphyrins 
Robert McGuire Jr., Dilek K. Dogutan, Thomas S. Teets, Jin Suntivich, Yang Shao-Horn and Daniel G. Nocera 
Chem. Sci., 2010, 1, 411 – 414, DOI: 10.1039/c0sc00281j 

Supramolecular hydrogel capsule showing prostate specific antigen-responsive function for sensing and targeting prostate cancer cells 
Masato Ikeda, Rika Ochi, Atsuhiko Wada and Itaru Hamachi 
Chem. Sci., 2010, 1, 491 – 498, DOI: 10.1039/c0sc00278j 

Total synthesis of all (-)-agelastatin alkaloids 
Mohammad Movassaghi, Dustin S. Siegel and Sunkyu Han 
Chem. Sci., 2010, DOI: 10.1039/c0sc00351d 

Pd-catalyzed ortho-arylation of phenylacetamides, benzamides, and anilides with simple arenes using sodium persulfate 
Charles S. Yeung, Xiaodan Zhao, Nadine Borduas and Vy M. Dong 
Chem. Sci., 2010, 1, 331 – 336, DOI: 10.1039/c0sc00231c 

Synthesis enables a structural revision of the Mycobacterium tuberculosis-produced diterpene, edaxadiene 
Jillian E. Spangler, Cheryl A. Carson and Erik J. Sorensen 
Chem. Sci., 2010, 1, 202 – 205, DOI: 10.1039/c0sc00284d 

DNA fluorocode: A single molecule, optical map of DNA with nanometre resolution 
Robert K. Neely, Peter Dedecker, Jun-ichi Hotta, Giedr Urbanaviit, Saulius Klimaauskas and Johan Hofkens 
Chem. Sci., 2010, 1, 453 – 460, DOI: 10.1039/c0sc00277a 

Diamine ligands in copper-catalyzed reactions 
David S. Surry and Stephen L. Buchwald 
Chem. Sci., 2010, 1, 13 – 31, DOI: 10.1039/c0sc00107d, Perspective 

The organocatalytic three-step total synthesis of (+)-frondosin B 
Maud Reiter, Staffan Torssell, Sandra Lee and David W. C. MacMillan 
Chem. Sci., 2010, 1, 37 – 42, DOI: 10.1039/c0sc00204f 

Direct observation of CuI/CuIII redox steps relevant to Ullmann-type coupling reactions 
Alicia Casitas, Amanda E. King, Teodor Parella, Miquel Costas, Shannon S. Stahl and Xavi Ribas 
Chem. Sci., 2010, 1, 326 – 330, DOI: 10.1039/c0sc00245c 

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Chemical Science? Then why not submit to us today or alternatively email us your suggestions.

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ChemComm Symposia – the journey

ChemComm Editor Robert Eagling reports the highs and lows of his journey to the 4th ChemComm International Symposium in Japan

As I set off for Japan and Korea I was eagerly looking forward to my first ChemComm symposium as Editor. At Heathrow I met up with Dr Luet Wong (University of Oxford), a speaker at the symposium, and the long trip to Osaka began (made even longer by a one hour delay for refuelling as we sat on the plane).

On arrival in Japan, the weather was grim, with low cloud and heavy rain – just what you need after a 12 hour flight. But on the plus side, the three hour journey from Tokyo to Osaka on the Bullet train was super efficient and on time to the second…just the Japanese way.

In Osaka it continued to rain contrary to the weather predictions. The hotel is fine; however, it amazes me, when WiFi is available in all McDonalds around the world, that a Sheraton hotel in a major city can not provide such a service.

Jet lag kicking in, we ventured out for dinner. With much choice, but everything in Japanese, the easy way is to just look at the pictures and plastic replicas. Despite the availability of a variety of Japanese restaurants, our final selection was a Chinese restaurant on the 12 floor of a department store. The food was great but after choosing a bottle of Chateau Bel Air, (from France and not Beverley Hills), the chilled glasses were sent back for room temperature equivalents. Alas, the wine was ice cold when delivered!

The final course of the meal was duck: four pieces of duck, enough for two, absolutely…. Unfortunately not, four pieces of duck skin, beautifully mounted on individual prawn crackers, great value at 2700 Yen (about £20).

Despite the duck, it was an excellent meal. Sensibly I retired to bed early in anticipation of a packed first day of stimulating lectures ahead…..

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Hot article round-up – September

FlamePhew! Other than the weather it has been a hot month here at Chemical Science. Here’s the monthly round up of the articles our referees thought were particularly exciting:

 

A couple of catalysts for coupling
Stephen Buchwald and colleagues report their studies on the use of two catalyst systems that provide the widest scope for palladium-catalysed C–N cross-coupling reactions to date. What were these systems? Find out in their Edge Article.

Frustrated about global warming?
Nitrous oxide is three times more potent a greenhouse gas than carbon dioxide and can hang around for over 150 years in the stratosphere. So Douglas Stephan and colleagues have been investigating how frustrated Lewis pairs interact with nitrous oxide with a view to converting the gas into a less environmentally harmful species. Read what they discovered in their Edge Article.

Additions to the molecular toolbox
The interaction of a sulfamate ester-derived metallonitrene with an allene generates a versatile intermediate with 2-amidoallylcation-like reactivity. In their Edge Article, Armin Stoll and Simon Blakey outline reactivity patterns for this novel dipolar species, demonstrating both [3 + 2] reactions with benzaldehyde, and unusual [3 + 3] annulation reactions with a variety of nitrones.

Economical extensions
The hydroxymethylation reaction is one of the most powerful and atom-economical one-carbon extension methods. Now Xiaoming Feng and colleagues have managed to hydroxymethylate unprotected oxindoles, which they say could provide practical and broadly applicable access to chiral linchpins bearing oxindoles. Find out how they did it in their Edge Article.

Mechanistic insights
Intermediates in gold(I)-catalysed cyclizations of enynes are not simple carbocations, say Antonio Echavarren and colleagues. They’ve investigated the mechanism of the gold-catalysed cyclopropanation of alkenes with 1,6-enynes, showing that it is stereospecific and mechanistically related to the Simmons-Smith reaction. Read all their insights in their Edge Article.

Let us know what you think of these articles by commenting below. And if you have your own hot research, submit it to Chemical Science today.

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