Seeding removes barrier to curious cocrystal

Michael Parkin writes on a HOT Chemical Science article in Chemistry World

After seven years of work, a team of chemists based in four labs across the globe has successfully prepared a cocrystal previously believed to be unobtainable.

Cocrystals are crystalline materials composed of two or more molecules held together within the same crystal lattice. Cocrystallisation is significant in the pharmaceutical industry, where drug molecules are screened for cocrystal formation in order to improve their solubility, stability and bioavailability. This has the added advantage of increasing the number of crystal forms that can be considered for drug formulation while simultaneously maximising patent protection.

Despite a computational study suggesting a stable cocrystal should form between caffeine and benzoic acid, all previous attempts over the last 60 years have failed. ‘When a cocrystal doesn’t form, we like to understand why that is – patients could miss out on better medical treatment if we miss out on crystal forms,’ says Dejan-Krešimir Bučar at the University of Cambridge in the UK, who led the study. ‘We hypothesised that a kinetic barrier hindered cocrystal formation, so our idea was to add a molecular species similar to that found in the nucleus of the caffeine·benzoic acid cocrystal as a seed to facilitate crystallisation.

Read the full article in Chemistry World»

Read the original journal article in Chemical Science:
The curious case of (caffeine)⋅(benzoic acid): How heteronuclear seeding allowed the formation of an elusive cocrystal
Dejan-Kresimir Bucar, Graeme Matthew Day, Ivan Halasz, Geoff G. Z. Zhang, John R. G. Sander, David G Reid, Leonard R. G. MacGillivray, M J Duer and William Jones  
Chem. Sci., 2013, Accepted Manuscript, DOI: 10.1039/C3SC51419F

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Nowhere for hydrazine to hide

Megan Tyler writes on a HOT Chemical Science article in Chemistry World

Scientists from the US and South Korea have developed a probe that can detect the highly toxic chemical hydrazine in a variety of different environments, including living cells.

Hydrazine plays an important role in a number of industrial processes. It’s used in pesticides, in nuclear and conventional electric power plants to reduce corrosion, and as a gas-forming agent in air bags. It’s even found in rocket fuel.

Although contact with small amounts of hydrazine is unlikely to cause harm, long term exposure can damage the liver, kidneys and central nervous system. Hydrazine has also been classified by the US Environmental Protection Agency (EPA) as a probable carcinogen.

Accidental leakage of hydrazine into the environment is rare and as hydrazine breaks down rapidly in oxygen, finding high levels of hydrazine in the environment is unlikely. However, hydrazine exposure in the workplace can be a real danger for individuals who come into contact with it. This makes the development of hydrazine sensors an important area of research.

The probe reacts with hydrazine to make a five-membered ring, resulting in a fluorescent response and a visible colour change

Read the full article in Chemistry World»

Read the original journal article in ChemComm:
Naphthalimide trifluoroacetyl acetonate: a hydrazine-selective chemodosimetric sensor
Min Hee Lee, Byungkwon Yoon, Jong Seung Kim and Jonathan L. Sessler  
Chem. Sci., 2013, Advance Article, DOI: 10.1039/C3SC51813B

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Destroying stable foam on demand

William Bergius writes on a HOT Chemical Science article in Chemistry World

The first example of stable and environmentally friendly foam that can be broken down by any one of three external stimuli has been developed by an international team of scientists.

From left to right: foam before and after an increase in temperature, UV irradiation and exposure to a magnetic field

Foams are commonly applied in the clean-up of chemical spills, where they are sprayed over large areas to prevent evaporation of volatile and harmful organic materials. While this demands stability, the foam then needs to be destabilised for transport due to its voluminous nature, often accomplished by the addition of an anti-foaming agent. The resulting liquid mixture can then be removed and the components recovered. Recent studies have tried to create stable foams which can be destabilised by external stimuli to remove the need for the addition of extra chemicals.

Orlin Velev and Stephanie Lam of North Carolina State University have collaborated with Anne-Laure Fameau from the French National Institute for Agricultural Research, to pool their multidisciplinary backgrounds in foams and emulsions, and colloids.

Read the full article in Chemistry World»

Read the original journal article in Chemical Science:
Multi-stimuli responsive foams combining particles and self-assembling fatty acids
Anne-Laure Fameau, Stephanie Lam and Orlin D. Velev  
Chem. Sci., 2013, Advance Article, DOI: 10.1039/C3SC51774H

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I challenge thee to a dual labelling

Our guest web writer Sarah Brown blogs about a HOT chemical biology paper on Chemical Science

Lift your right foot off the floor and make clockwise circles with it. Managing comfortably? Now draw a ‘6’ in the air with your right hand – what’s happened to your foot? It’s all gone a bit wrong, hasn’t it? See, it isn’t that easy to do two different things at once. Another example of this is the dual labelling of proteins; however, Stephen Caddick and colleagues appear to have got on top of this, as reported in their recent paper in Chemical Science.

The dual labelling of proteins has the potential to enable studies of protein structures and the construction of theranostics, for example; however, proteins can be complex and modifications are often restricted to the N- and C-termini, limiting their usefulness. Modification of non-terminal positions is tricky and can be slow, expensive and unrewarding. Caddick and colleagues demonstrate a novel approach to site-selective labelling of proteins, which yields a dual-labelled product by the introduction of two cysteine mutants into the sequence, which are converted by a single chemical reagent into two distinct products for modification. One residue, with an accessible alpha-proton, readily forms dehydroalanine, and the other residue persists, by shielding, as a sulfonium that undergoes chemoselective ring opening by reaction with an azide group. Both groups can then be further labelled orthogonally by the desired molecules.

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The group demonstrated their technique by modifying GFP (green fluorescent protein). After incorporation of the cysteine mutants and treatment with a chemical reagent (2, 5-dibromohexanediamide), further treatment with sodium azide generated dual modified GFP. Further reaction with an alkyne modified dye and mercaptoethanol yielded a rhodamine dye and thiol-labelled protein.

The researchers have demonstrated a site- and chemoselective method, which they say offers a facile and generally accessible technique for dual labelling. And now they’ve got to grips with that, I pose the ultimate test: to come up with a facile method for standing on one leg and drawing a ‘6’ – trying to do that and type this blog has also been pretty challenging.

Once you’ve tried out some one-legged multi-tasking, sit back down and read this Open Access Edge Article to see what Sarah’s talking about:

A novel approach to the site-selective dual labelling of a protein via chemoselective cysteine modification
Ramiz I. Nathani, Paul Moody, Vijay Chudasama, Mark E. B. Smith, Richard J. Fitzmaurice and  Stephen Caddick
Chem. Sci., 2013, 4, 3455-3458
DOI: 10.1039/C3SC51333E

Sarah Brown is a guest web-writer for Chemical Science.  Sarah hung up her lab coat after finishing her PhD and post-doctorate in nanotechnology for diagnostics and therapeutics and now works in scientific publishing. When not trying to explain science through ridiculous analogies, you can often find her crocheting, baking or climbing, but not all at once. All views are her own.

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HOT Chem Sci articles for July

Here are this month’s referee-recommended HOT Chemical Science articles– download them for FREE for a limited time! Come back and check this post for more HOT articles!

Palladium-catalyzed heteroallylation of unactivated alkenes – synthesis of citalopram
Joanne F. M. Hewitt, Lewis Williams, Pooja Aggarwal, Craig D. Smith and David J. France
Chem. Sci., 2013, 4, 3538-3543
DOI: 10.1039/C3SC51222C, Edge Article

C3SC51222C ga

Free to access until 25th August 2013


Seeing through solvent effects using molecular balances
Ioulia K. Mati, Catherine Adam and Scott L. Cockroft
Chem. Sci., 2013, Advance Article
DOI: 10.1039/C3SC51764K, Edge Article

C3SC51764K ga

Free to access until 25th August 2013

Click here for more free HOT Chemical Science articles for July!

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Inaugural Chemical Science Lectureship announced

We are delighted to announce the winner of the inaugural Chemical Science Lectureship – Professor Kevan Shokat.

The 2013 Chemical Science Lectureship was awarded in the area of chemical biology and the award lecture was given at Challenges in Chemical Biology (ISACS11) in Boston, USA, in July. Professor Shokat was presented with his award by Chemical Science Associate Editor, Professor Tom Muir.

Shokat

Tom Muir presenting Kevan Shokat with his Chemical Science Lectureship at ISACS11

Professor Shokat obtained his Ph.D. at UC Berkeley and following appointments at Stanford University and Princeton University, in 1999 he moved to UC San Francisco to his current appointment as Associate Professor of Cellular and Molecular Pharmacology.

The Shokat Lab’s research is focused on using the tools of synthetic organic chemistry, structural biology, genetics, and mathematical modelling to gain insight into how signalling networks transmit information in normal and disease settings. Their guiding principle is to use chemistry to answer questions that cannot be addressed by the use of biochemistry or genetics— they seek to provide tools, which fill in the gaps left behind by more traditional approaches.

Award Details
The lectureship, which will be awarded annually, will recognize sustained excellence in research by a mid-career scientist within the chemical sciences. The recipient of the Lectureship is selected and endorsed by the Chemical Science Editorial Board.

The recipient will be invited to present a plenary lecture at a relevant International Symposia on Advancing the Chemical Sciences (ISACS); they will also receive a certificate, $2000 and will be invited to contribute to Chemical Science.

The 2014 Chemical Science Lectureship winner will give a plenary lecture at one of the 2014 ISACS meetings:

  • ISACS 13: Challenges in Inorganic Chemistry and Materials Chemistry – July 2014, Dublin, Ireland
  • ISACS 14: Challenges in Organic Chemistry (Synthesis) – August 2014, Shanghai, China
  • ISACS 15: Challenges in Nanoscience – August 2014, San Diego, USA

More information about these conferences will appear on the ISACS website soon.

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Challenges in Chemical Renewable Energy (ISACS12) – final registration 5 Aug

Final Registration Deadline – 5 August 2013

You have just a few days left to secure a place at the 12th conference in the International Symposia on Advancing the Chemical Sciences (ISACS) series as registration for Challenges in Chemical Renewable Energy (ISACS12) closes on Monday 5 August 2013.

Don’t miss your opportunity to join outstanding researchers from across the globe to explore the themes of photovoltaics, solar fuels, new battery materials, fuel cells and molecular catalysis.

Registration is quick and simple via the online booking system and spaces are filling up fast so be sure to guarantee yours now.

Programme Live

We are pleased to announce that the ISACS12 programme is now available to view online. Take a look at the schedule to discover the full speaker line up and stimulating lecture titles over the entire four days. 

Find Out More

For the latest information on Challenges in Chemical Renewable Energy (ISACS12) or any of the conferences in the series, please follow ISACS on twitter or visit the dedicated webpage.

We look forward to welcoming you to Cambridge.

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Long-life lithium sulfide batteries

Jeanne Therese Andres writes on a HOT Chemical Science article in Chemistry World

Scientists from the US and China have identified a polymer that makes lithium sulfide batteries last longer.

Electric powered car sign

 Amongst batteries in-use today, lithium ion ones produce more energy per unit mass than most others. However, electric vehicles demand even higher energy batteries with longer charge intervals.

Lithium sulfide batteries can hold much more energy than present-day lithium ion batteries but are limited by their short battery life. This is due to an irregular dispersion of lithium in their electrode slurry, as well as soluble polysulfides being lost when they dissolve in the electrolyte.

Initial numerical modelling followed by lab tests lead Yi Cui at Stanford University and his co-workers to discover that polyvinylpyrrolidone (PVP) can be used to hold a battery’s lithium sulfide and polysulfides during cycling. The PVP allows lithium ions…

Read the full article in Chemistry World»

Read the original journal article in Chemical Science:
Stable cycling of lithium sulfide cathodes through strong affinity with a bifunctional binder
Zhi Wei Seh, Qianfan Zhang, Weiyang Li, Guangyuan Zheng, Hongbin Yao and Yi Cui  
Chem. Sci., 2013, 4, 3673-3677
DOI: 10.1039/C3SC51476E, Edge Article

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Lowering a barrier for heterogeneous catalysis

Heterogeneous catalysis is widely used industrially to assist in the production of many man made materials.  The world economy is reliant upon production of these materials, therefore catalysts which are reliable and cheap are hugely important.  Heterogeneous catalysts generally fulfill these criteria, hence their wide application, but the understanding of how they function is often poorly defined.

Academic investigations of single site homogeneous catalysts are generally simpler to study, which makes defining what reactions occurs at each stage and the factors which influence them clearer to interpret.  Heterogeneous catalysts are more complex to study.  The interaction between the different phases must be considered along with the nature of the catalyst itself.  The catalysts are generally solid materials whose bulk composition may not provide an accurate picture of the surface where the reactions will ultimately be occurring and the activity may be quite different.  Analysis of the subtleties of what is happening at the surface is incredibly difficult with many of the commonly used techniques not capable of providing the detail required.  But in order to fully understand a heterogeneous catalyst it is essential to have an understanding of the how the separate phases interact.

Tristan Youngs of the ISIS Facility, Christopher Hardacre of Queen’s University Belfast, and their co-workers have reported a new method to study a heterogenous process in real time.  Neutron scattering experiments (which were only made possible by the state of the art facilities at ISIS) provide the ability to simultaneously examine the rate at which reactions occur and also the speed with which the different phases in a heterogeneous system can interact.  A commonly held principle of heterogeneous catalysis is that by constructing pores and channels in the catalyst we can increase the effective surface area of the catalyst, increasing the number of sites where reactions can occur, thereby increasing the effectiveness of the catalysts.

This study, for the first time, highlights that the speed of the process is critically dependent on how easily the molecules can pass in and out of these pores.  While this may not be the case for every process, challenging some of these commonly held beliefs will surely lead to a rethink of how catalysts are designed in the future.

Interested in more?  Read this HOT, Open Access Chem Sci Edge article now!

Probing chemistry and kinetics of reactions in heterogeneous catalysts
Tristan G. A. Youngs, Haresh Manyar,  Daniel T. Bowron,  Lynn F. Gladden and Christopher Hardacre
Chem. Sci., 2013, Advance Article
DOI: 10.1039/C3SC51477C

Ruaraidh McIntosh is a guest web-writer for Chemical Science.  His research interests include supramolecular chemistry and catalysis.  When not working as a Research Fellow at Heriot-Watt University, Ruaraidh can usually be found in the kitchen where he has found a secondary application for his redoubtable skills in burning and profanity.

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Chem Sci articles in 2013 Cancer Nanotechnology collection– free till 28 July

We are pleased to present a web collection of articles from publications across the RSC journal portfolio demonstrating the use of (nano)technology in the diagnosis, imaging and treatment of cancer.

This web collection will be free to access until the 28th July, so register for an RSC Publishing personal account and read this cutting edge research for free this week!

Read these Chemical Science Edge Articles as part of this special cancer nanotechnology collection:

A platinum anticancer theranostic agent with magnetic targeting potential derived from maghemite nanoparticles
Jinzhuan Wang, Xiaoyong Wang, Yajie Song, Jing Wang, Changli Zhang, Cunjie Chang, Jun Yan, Lin Qiu, Mingmin Wu and Zijian Guo
Chem. Sci., 2013,4, 2605-2612
DOI: 10.1039/C3SC50554E

Graphical abstract: A platinum anticancer theranostic agent with magnetic targeting potential derived from maghemite nanoparticles

Poly(ethylene oxide)-block-polyphosphester-based paclitaxel conjugates as a platform for ultra-high paclitaxel-loaded multifunctional nanoparticles
Shiyi Zhang, Jiong Zou, Mahmoud Elsabahy, Amolkumar Karwa, Ang Li, Dennis A. Moore, Richard B. Dorshow and Karen L. Wooley
Chem. Sci., 2013,4, 2122-2126
DOI: 10.1039/C3SC50252J

Graphical abstract: Poly(ethylene oxide)-block-polyphosphester-based paclitaxel conjugates as a platform for ultra-high paclitaxel-loaded multifunctional nanoparticles

Lipid-coated nanoscale coordination polymers for targeted delivery of antifolates to cancer cells
Rachel C. Huxford, Kathryn E. deKrafft, William S. Boyle, Demin Liu and Wenbin Lin
Chem. Sci., 2012,3, 198-204
DOI: 10.1039/C1SC00499A

Graphical abstract: Lipid-coated nanoscale coordination polymers for targeted delivery of antifolates to cancer cells

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