Ready to order? Yes, I’ll have the extra cold superconducting penne, please…

Written by guest web-writer Kevin Murnaghan.

In this highly original work, researchers from the Complex Functional Materials Group at the University of Bristol and the Superconductivity and Magnetism Group at the University of Warwick have used off-the-shelf, supermarket pasta as a sacrificial template for the production of a variety of superconducting wires, tubes and spirals.  They have even made a superconducting ‘jolly roger’ skull and crossbones.

Here’s how: The pasta was pre-washed to remove impurities and then rehydrated in a solution containing a mixture of nitrates of yttrium, barium and copper. A slight excess of barium nitrate was used to make sure the desired superconducting material YBa2Cu2O7-x phase (Y123) was attained. Via a calcination process the superconducting pasta shapes were produced, removing the organic material of the sacrificial template and neatly retaining the macroscopic shape of the template.

C3CC38271K_graphical abstract

‘Chemical black pepper and parmesan’ were provided by the use of silver nitrate in the process, which boosts electrical and structural properties. Without using this salt, structures formed are brittle, but with it, compressive strength of the shapes doubled in strength from 0.76 to 1.56 MPa.  This helped counteract the effect of porosity formed from the outgassing of the sacrificial pasta during the calcination process.

Interestingly, the pasta had its own influence on the properties of the material.  Starch-mediated reduction of Ag(I) to Ag(0) is the reason for the dark colour of the materials formed, and trace transition metals in the foodstuff were found to have an effect on electrical and superconducting properties.

Critical temperatures, Tc and current densities, Jc, in early samples were found to be low, relative to typical Y123 type superconductors when silver was not included in the synthesis, and were markedly improved when it was.  Further improvements to the superconductivity of the spaghetti-based replicas were achieved via sintering and annealing.  This work represents a highly cost-effective route to a range of superconducting materials with macroscopic architectures, compared with current state of the art processes such as CVD or PLD.  Future work will focus, in part, on further densification of the product, and purity of the sacrificial template.  Further fascinating information is provided in the electronic supplementary information.  Buon appetito!

C3CC38271K_coverRead this ChemComm cover article today:

Designed 3D architectures of high-temperature superconductors

David C. Green, Martin R. Lees and Simon R. Hall
Chem. Commun., 2013,49, 2974-2976
DOI: 10.1039/C3CC38271K

Kevin Murnaghan is a guest web-writer for Chemical Communications. He is currently a Research Chemist in the Adhesive Technologies Business Sector of Henkel AG & Co. KGaA, based in Düsseldorf, Germany. His research interests focus primarily on enabling chemistries and technologies for next generation adhesives and surface treatments. Any views expressed here are his personal ones and not those of Henkel AG & Co. KGaA.

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11th International Conference on Materials Chemistry (MC11)– Registration now open!

We are delighted to announce that registration for the 11th International Conference on Materials Chemistry (MC11) is now open.

Why take part in this conference?

In the 20th year of this international Materials Chemistry conference series, this meeting will bring together researchers from across this exciting field to discuss four key areas of application of materials chemistry:

  • Energy Materials – including all aspects of Materials Chemistry related to energy generation, conversion and storage.
  • Environmental Materials – the design, synthesis and applications of materials that facilitate processes to provide a sustainable environment.
  • Biomaterials – materials for tissue engineering and healthcare, green biomaterials and advanced synthesis methods of biomaterials.
  • Electronic, Magnetic and Optical Materials – encompassing inorganic, organic, hybrid and nano materials, soft matter and interfaces.

Registering early guarantees you an early bird discount of £50 – so register now!  And you can showcase your own work by presenting a poster.

MC11 will appeal to academic and industrial scientists working on the chemistry, physics and materials science of functional materials.  Come and hear the best in the field and take advantage of many opportunities for discussion with other researchers in materials chemistry.

For more information visit: http://rsc.li/mc11

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If you like it, then you should put two rings on it

Microring resonators are pretty amazing things, offering label-free biosensing by coupling with light and then circulating the photons inside the cavity of the ring, enhancing the interaction between the light and the analytes.

However, I like to think of traditional microring resonators as tents: difficult to construct. They require a submicrometer gap between the input waveguide and the resonator ring structure to allow the coupling of light and before you can even get to that stage, you need to make the microring resonator, which requires a series of complex fabrication steps (FIG 1a).  In this Communication, which is part of ChemComm‘s Microfluidics themed web collection, Professor Jonathan Cooper and his colleagues at Glasgow University and at the International Islamic University Malaysia’s CTS Department have made (what I think of as) the double pop-up tent equivalent– or as they call it, the dual disk resonator (DDR). Made from SU8, an epoxy-based polymer used in microfluidics chips, it can be patterned in a single lithographic step. Not only that, but the DDR uses a gapless design and two rings, increasing the sensitivity of the device (FIG 1b).

FIG 1: The hard way or the easy way (a) the traditional microring resonator with submicrometer gap (b) gapless dual disk resonator

Once they had constructed the DDR, the team characterised the optical sensitivity of the device using sucrose solutions to vary the refractive index of the sample above the waveguide. They then went on to show that the sensor could be used to evaluate the dynamics of antibody interactions on surfaces, exploring avidin-biotin-based immobilisations; sharp resonance shifts confirmed the assembly and disassembly of constructs.

The simpler fabrication shows great promise, as the authors suggest that the sensitivity of the device could be greatly improved by coupling more disks to it– in which case Beyoncé might soon be singing ‘if you like it, then you should put a chain on it.’

Read this ‘HOT’ ChemComm article today:

Polymer dual ring resonators for label-free optical biosensing using microfluidics

Muhammad H. M. Salleh, Andrew Glidle, Marc Sorel, Julien Reboud and Jonathan M. Cooper

Chem. Commun., 2013, Advance Article

DOI: 10.1039/C3CC38228A

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Harnessing enzyme-substrate specificity for gel-based sensors

Gels that are held together by non-covalent interactions are a hot topic in supramolecular chemistry.  In this Communication, Itaru Hamachi’s research group from Kyoto University report a series of glycolipids that form  yellow hydrogels from orange suspensions when heated. The gelation and hence the colour change is reversible, and the authors hoped to use this response to create a sensor system.

Hamachi's gelator molecules

Once the gel has formed, adding a glycosidase enzyme which can selectively cleave the β-glucosidic bond leads to breakup of the gel and a colour change from yellow to orange. This response is only observed with an enzyme that is complimentary to the saccharide used as a “substrate unit” in the gelator. Hence, the authors have harnessed natural enzyme-substrate selectivity to yield a highly selective sensing system. The combination of a number of these gels into a sensor array chip yields a system that can simply and rapidly detect and distinguish a range of glycosidase enzymes. The ability to selectively sense these enzymes could have significant application for diagnosing disease and identifying bacterial contamination of drinking water.

Hamichi's sensor array

Read this ‘HOT’ ChemComm article today:

Supramolecular hydrogels based on bola-amphiphilic glycolipids showing color change in response to glycosidases

Rika Ochi, Kazuya Kurotani, Masato Ikeda, Shigeki Kiyonaka and Itaru Hamachi

Chem. Commun., 2013, 49, 2115-2117

DOI: 10.1039/C2CC37908B

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Removing toxic chemicals with POPs

The filters used in gas masks, which give protection against toxic industrial chemicals, are often large and cumbersome, being made from activated carbon that is impregnated with metal salts. In a search for alternatives, SonBinh Nguyen and colleagues at Northwestern University, Evanston, Illinois, have joined forces with scientists at the Edgewood Chemical Biological Center, Maryland, to investigate a series of porous organic polymers (POPs) bearing metal-catecholate groups. By changing the molecular components used in their synthesis, the materials have been tailored to hydrogen bond to, and consequently eliminate, specific toxic industrial chemicals, like ammonia.

‘Metal-organic frameworks (MOFs) have the same customisable characteristics as POPs, and have been investigated for their ability to remove toxic chemicals,’ says Nguyen. ‘Yet many of the MOFs known today are not very stable, owing to the prevalence of metal-oxygen bonds, and will degrade in the presence of atmospheric moisture. POPs, on the other hand, contain carbon-carbon bonds, which are less susceptible to moisture attack,’ he explains.

Chemical reaction

Read the full article in Chemistry World

Read the original journal article in ChemComm:
Removal of airborne toxic chemicals by porous organic polymers containing metal–catecholate
Mitchell H. Weston, Gregory W. Peterson, Matthew A. Browe, Paulette Jones, Omar K. Farha, Joseph T. Hupp and SonBinh T. Nguyen
Chem. Commun., 2013, Advance Article
DOI: 10.1039/C3CC40475G

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23rd International Symposium: Synthesis in Organic Chemistry

The deadline for submitting poster abstracts for the 23rd International Symposium: Synthesis in Organic Chemistry is fast approaching – 11 March 2013.

The Synthesis in Organic Chemistry conference is the flagship event of the RSC’s Organic Division. This conference will provide an international showcase for the core area of organic chemistry – synthesis – covering all aspects of contemporary organic synthesis and providing a forum for the ever more exciting methodologies and strategies that continue to emerge.

Don’t miss out – reserve your poster presentation space for a chance to showcase your own work, and register early to take advantage of the £50 saving on the standard fee.

Remember too that there are a limited number of bursaries on offer for students and younger members of the RSC in the early stages of their career – worth £150.

Make sure you take the opportunity to join us to hear outstanding speakers across the many themes of the symposium in an extremely stimulating programme of plenary and keynote lectures.

Check out the event website to find out more – http://rsc.li/os23

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Combating Influenza: Anthraquinone–Sialic Acid Hybrids for the Inhibition of Viral Neuraminidase

In the fight against influenza, viral neuraminidase (NA) represents an important target. This enzyme is essential for the replication of the virus, and its inhibition can prevent the spread of the disease. Scientists at Keio University have now identified a set of novel anthraquinone–sialic acid hybrids which can inhibit influenza virus neuraminidase with photo-irradiation under neutral conditions.

Anthraquinone derivatives were found to degrade proteins when subjected to photo-irradiation; this degradation is likely caused by hydroxy radicals which are produced from the photolysis of anthraquinone and oxygen. Crucially, researchers led by Prof. Kazunobu Toshima proposed that NA-inhibition could be obtained if such an anthraquinone derivative could be tethered to an NA-binding moiety. Sialic acid is a native ligand for NA— both “normal” NA and drug-resistant NA— and so researchers prepared and investigated a number of anthraquinone–sialic acid hybrids (1–3).

These hybrids were found to be effective for the inhibition of NA under photo-irradiation, and interestingly, showed comparable or superior results compared to the leading anti-NA drug, especially in the inhibition of drug-resistant NA. While further tests are ongoing, this research represents an important advance in influenza treatment, and offers great potential for the inhibition of other disease targets.

For more, read this ‘HOT’ ChemComm article in full:

Photodegradation and inhibition of drug-resistant influenza virus neuraminidase using anthraquinone–sialic acid hybrids

Yusuke Aoki,  Shuho Tanimoto,  Daisuke Takahashi and Kazunobu Toshima
Chem. Commun., 2013, 49, 1169–1171
DOI: 10.1039/C2CC38742E
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A new system for cancer detection

While current cancer-diagnosis methods rely on an invasive biopsy or the detection of cancer-specific biomarkers, South Korean scientists have developed a simple and non-invasive detector for cancer cells that could speed up the early diagnosis of the condition, leading to a greater chance of survival for cancer patients.

Cancer cells fluorescing

Daunomycin interacting cancer cells viewed with fluorescene microscopy

Cancer cells have been found to differ from normal cells in several ways, including the make up of their cell membranes. Cancer-cell membranes have been found to contain more anionic lipids than normal cells, leading to an overall negatively charged cell surface. Yoon-Bo Shim and co-workers from Pusan National University, have exploited this negative surface charge to develop a probe based on daunomycin, an anti-cancer drug that is known to interact strongly with anionic lipids.

Read the full article in Chemistry World.

Read the original journal article:
Cancer cell detection based on the interaction between an anticancer drug and cell membrane components
Chem. Commun., 2013, 49, 1900-1902
DOI: 10.1039/C2CC38235K

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Penny Brothers joins ChemComm as Associate Editor

ChemComm warmly welcomes Professor Penny Brothers (University of Auckland, New Zealand) as a new Associate Editor. 

Penny Brothers is now accepting submissions to ChemComm in the areas of porphyrin chemistry, the main group elements and organometallic chemistry.  Her current research interests also include the chemistry of new sustainable materials and inorganic medicinal chemistry. 

Submit your next top-notch, high-impact Communication to Penny Brother’s Editorial Office.

Biography

Penny Brothers was born and grew up in Auckland, New Zealand, and completed her BSc and MSc(Hons) degrees in chemistry at the University of Auckland.  In 1979 she was awarded a Fulbright Fellowship and set off for Stanford University to begin a PhD in chemistry under the supervision of Professor Jim Collman.  Her PhD thesis, and much of her subsequent research work, has centered around the chemistry of porphyrin complexes.Professor Penny Brothers

In 1986 she returned to Auckland and spent two years working as a postdoctoral fellow with Professor Warren Roper in the Department of Chemistry, focussing on organometallic chemistry.  In 1988 she took up her current academic position at the University of Auckland.

She has been a visiting scientist at Los Alamos National Laboratory (2003, 2005, 2006) and a visiting professor at the University of California at Davis (1993), the University of Heidelberg (2003) and the University of Burgundy (2004, 2006).  She has been awarded a Fulbright Senior Scholar Award for 2007.

Her current research brings together her interests in porphyrin chemistry, the main group elements and organometallic chemistry.  She investigates how the porphyrin ligand can be used to modify the chemistry of elements such as boron and bismuth, and as a ligand in complexes containing unusual chemical bonds between transition metal and main group elements.  She has a number of research collaborations in NZ and internationally.

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Novel silicon-mediated transannular cyclopropanation

An intriguing new method of transannular cyclopropanation has been reported by Prof. James Dowden‘s group at the University of Nottingham. This cyclopropanation, mediated by the presence of a trimethylsilyl group, allows the rapid formation of 4-azabicyclo(5.1.0)octenones (3) from simple starting materials. Divinyl beta-lactam (1) was elegantly formed via a Staudinger cycloaddition reaction beginning from 3-trimethylsilylpropenal, 4-methoxyaniline and crotonyl chloride. Next, researchers were able to transform 1 into dihydroazocinone (2) using a thermal Cope rearrangement.

The Dowden group discovered that if 2 was treated with TBAF or aqueous sodium hydroxide, 4-azabicyclo(5.1.0)octenone (3) could be formed. Interestingly, the reaction was dependent on the presence of the silicon group; when the trimethylsilyl group was replaced with an ester, no cyclopropanation occurred. The researchers proposed that the transannular cyclopropanation could be viewed as a Lewis-base–promoted Hosomi–Sakurai reaction proceeding via intramolecular 1,4-conjugate addition. 4-azabicyclo(5.1.0)octenones (3) are an unusual structural motif and it is hoped that this facile method for their construction may facilitate further examination of chemical space interactions.

Read this ‘HOT’ Chem Comm article today:

An unusual silicon mediated transannular cyclopropanation

Bing You,  Kate Hamer,  William Lewis and James Dowden
Chem. Commun., 2013, 49, 795-797
DOI: 10.1039/C2CC37739J
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