Archive for the ‘News’ Category

RSC Publishing Recognises Outstanding ChemComm Achievements in China

This week Dr James Milne (RSC Publishing) presented a certificate of achievement to Professor Hongjie Zhang, at Changchun Institute of Applied Chemistry. 

Professor Zhang was recognised for his prolific published research over the last year. RSC has published 17 of Professor Zhang’s papers – making him the most successful author from China during the year and three of these papers were published in ChemComm

Read Professor Zhang’s excellent work published in ChemComm: 

High intensity focused ultrasound and redox dual responsive polymer micelles
Yongwen Li, Rui Tong, Hesheng Xia, Hongji Zhang and Juan Xuan, Chem. Commun., 2010, 46, 7739-7741 (DOI: 10.1039/C0CC02628J)

Selective synthesis of dibenzo[a,c]cyclooctatetraenes via palladium-catalyzed [4+4] cyclic homocoupling of borylvinyl iodobenzene derivatives
Hui-jun Zhang, Junnian Wei, Fei Zhao, Yun Liang, Zitao Wang and Zhenfeng Xi, Chem. Commun., 2010, 46, 7439-7441 (DOI: 10.1039/C0CC02380A)

Making a [Co24] metallamacrocycle from the shuttlecock-like tetranuclear cobalt-calixarene building blocks
Yanfeng Bi, Guancheng Xu, Wuping Liao, Shangchao Du, Xinwu Wang, Ruiping Deng, Hongjie Zhang and Song Gao, Chem. Commun., 2010, 46, 6362-6364 (DOI: 10.1039/C0CC01844A)

Dr Milne and Dr Daping Zhang (RSC Publisher, China) are on a tour of China where they will visit seven universities/institutes and four companies in Beijing, Changchun, Shanghai and Xiamen.

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New tool for speeding up porous materials discovery

A new tool (Infrasorb-12) for screening porosity has been developed by scientists in Germany. The tool identifies high surface area materials in a very short time with high accuracy.  The researchers say that Infrasorb-12 development will speed up the discovery of new porous materials significantly and broaden the wide range of materials suitable for gas storage, selective adsorption, catalysis, and life science applications.

Further information:
High-throughput screening: speeding up porous materials discovery
Philipp Wollmann, Matthias Leistner, Ulrich Stoeck, Ronny Grünker, Kristina Gedrich, Nicole Klein, Oliver Throl, Wulf Grählert, Irena Senkovska, Frieder Dreisbach and Stefan Kaskel, Chem. Commun., 2011, DOI: 10.1039/C1CC10674K

Also of interest:
Modifying MOFs: new chemistry, new materials
Seth M. Cohen, Chem. Sci., 2010, 1, 32-36 (DOI: 10.1039/C0SC00127A)

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Carbon dioxide adsorption in porous phosphine coordination material

US, UK and Korean scientists have made a new porous phosphine coordination material, PCM-11. The material is an unusual 8,4-connected coordination polymer with an open 3-D pore structure, say the researchers. 

The team formed the material by reacting Mg(II) with tris(para-carboxylato)triphenylphosphine oxide. The highly ionic nature of the metal–ligand bonding results in excellent thermal stability upon desolvation (>460 ºC), they say. PCM-11 is easily activated for small molecule sorption at low temperature without the requirement for solvent pre-exchange.  It adsorbs 47.5 wt% CO2 at 11.6 bar and 30ºC.

Find out more in the ChemComm communication:
High capacity CO2 adsorption in a Mg(II)-based phosphine oxide coordination material
Alisha M. Bohnsack, Ilich A. Ibarra, Peter W. Hatfield, Ji Woong Yoon, Young Kyu Hwang, Jong-San Chang and Simon M. Humphrey, Chem. Commun., 2011, DOI: 10.1039/C1CC10754B

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Breathe out for personalised medicine

A method to analyse drug levels in the body could allow people with epilepsy to avoid weeks of blood tests, claim scientists from Switzerland.

Valproic acid is an anticonvulsant drug used in the treatment of epilepsy; however, in the body, the acid binds to proteins and the concentration also can be influenced by over-the-counter medicines. The variations in the concentration mean that the amount of pharmacologically relevant valproic acid needs to be carefully monitored for the first few weeks and the dosage adjusted to compensate. The concentration is normally measured using blood samples from patients, and it can take a long time for the results to come back.

Now, Renato Zenobi at the Swiss Federal Institute of Technology in Zurich and co-workers have developed a method to measure valproic acid metabolite levels in breath using electrospray mass-spectrometry.

 
Using a breath test, scientists can measure levels of the anticonvulsant drug valproic acid in the body to determine the correct dosage for individual patients

See Chemistry World for the full news story 

Link to journal article
Real-time, in vivo monitoring and pharmacokinetics of valproic acid via a novel biomarker in exhaled breath
Gerardo Gamez, Liang Zhu, Andreas Disko, Huanwen Chen, Vladimir Azov, Konstantin Chingin, Günter Krämer and Renato Zenobi
Chem. Commun., 2011, DOI: 10.1039/c1cc10343a

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Congratulations to Jean-François Nierengarten

Jean-François NierengartenWhat’s special about Gene delivery with polycationic fullerene hexakis-adducts?

Well, that’s the topic of Jean-François Nierengarten’s recent ChemComm communication, rated as ‘hot’ by the referees and free to access* until 15th March. It is also his 25th independent research article in ChemComm.

To celebrate this achievement, Professor Nierengarten has taken some time out from his research to speak to ChemComm about his career.

What inspired you to become a scientist?
As far as I remember, I was always fascinated by natural sciences and wildlife. I started to study biology at the University of Strasbourg (Université Louis Pasteur at that time) with the idea of becoming a zoologist to discover unknown animals in the Amazon rainforest or in other wild places in the world. On the way, I discovered chemistry thanks to a couple of outstanding teachers and definitively switched from biology to chemistry after I met Jean-Pierre Sauvage at the end of my first year of Master. Fortunately, after my Master, I had the chance to prepare my PhD under the guidance of Jean-Pierre, and thus to become a chemist.

What was your motivation behind the work described in your ChemComm article?
The work described in this paper is a part of our research program on the use of click chemistry for the post-functionalisation of fullerene hexa-adducts (Chem. Commun. 2008, 2450; 2010, 46, 3860 and 4160; 2011, 47, 1321). The initial driving force for this work was to apply the synthetic methodology developed in the group to the preparation of new molecules with specific properties. As very often happens, applications with our compounds rely on collaborations with colleagues having the appropriate expertise. Indeed, Jean-Serge Remy, a well-established scientist in the field of transfection and synthetic vectors, is a very good friend and discussing about science one Friday evening in a pub brought us to the idea of testing fullerene hexa-adducts as synthetic vectors. We thus prepared a series of hexa-substituted fullerene derivatives decorated with dendritic branches bearing peripheral ammonium groups. Jean-Serge and his co-workers could then show that polyplexes prepared from DNA and these globular polycationic fullerene derivatives exhibit remarkable gene delivery capabilities. This result was quite unexpected as a generally admitted rule for the design of gene delivery vectors is that compact globular polycations with an isotropic distribution of positive charges are not suitable candidates for such studies. The results reported in our ChemComm article show that this is indeed not the case.

Why did you choose ChemComm to publish your work?
For fast publication of our important findings, ChemComm is an obvious choice. Over the years, it has been always a pleasure to work with the RSC Journals in general and with ChemComm in particular. All the steps from the submission to the publication are very efficient and all is organized in a very professional way. Publishing our work in ChemComm is also the guarantee for high visibility. Finally, I am a supporter of European journals in general and strongly believe that the best of European chemistry should be reported in European journals. Having top quality journals in Europe is essential to give credit to the European chemical community.

Where do you see your research heading next?
In addition to their remarkable gene delivery capabilities, the fullerene hexa-adduct derivatives have also revealed a very low toxicity if any. The fullerene hexa-adduct core is therefore a particularly appealing 3D-scaffold for the development of new multifunctional bioactive molecules. Based on the versatile fullerene hexa-adduct building blocks already developed in our group (Chem. Commun. 2010, 46, 4160), the successive grafting of up to three different groups on the fullerene core can be efficiently achieved. We are currently working on a new generation of vectors bearing targeting subunits for specific gene delivery to selected cells and/or fluorescent probes to monitor their intracellular pathway by confocal microscopy.

What do enjoy doing in your spare time?
Spending time with Iwona, my wife, and our two kids, cooking, listening to music, travelling. I like also reading and playing the guitar but have less and less time for it!

What would you be if you weren’t a scientist?
Hopefully as happy as I am to be a scientist! I guess that it could be the case if I would be an ébéniste [cabinet maker]. During my childhood, I had a lot of fun making stuff from wood in the workshop of my godfather, a very talented ébéniste particularly gifted for marquetry. I could spend hours watching him applying pieces of veneer to form decorative patterns or pictures onto the commodes or the tables he was restoring.

Also of interest:
Less is more – multiscale modelling of self-assembling multivalency and its impact on DNA binding and gene delivery
Paola Posocco, Sabrina Pricl, Simon Jones, Anna Barnard and David K. Smith
Chem. Sci., 2010, 1, 393-404

*Access our free content any time, any place – register for an RSC Publishing personal account today

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Announcing the ChemComm Emerging Investigators issue 2012

Following the success of the inaugural ChemComm Emerging Investigators issue, we are delighted to announce the forthcoming 2012 Emerging Investigators issue. All interested parties should contact the ChemComm Editorial Office in the first instance.

This issue is dedicated to profiling the very best research from scientists in the early stages of their independent careers from across the chemical sciences. We hope to feature principal investigators whose work has the potential to influence future directions in science or result in new and exciting developments.

 

Also of interest:
ChemComm Emerging Investigator Lectureship:
Submit your nominations by 28th February 2011

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Sleeping Trojan horse to transport metal ions into cancer cells

UK researchers have used a cage-like molecule to smuggle metal ions into cells, which could improve medical imaging.

Medical imaging often requires getting unnatural materials such as metal ions into cells. Scientists have therefore had to come up with ways to disguise these compounds to get them past the cell membranes. Michael Coogan and colleagues at Cardiff University have come up with a way to avoid the current difficulties with some of these imaging treatments.

Graphical abstract: A ‘Sleeping Trojan Horse’ which transports metal ions into cells, localises in nucleoli, and has potential for bimodal fluorescence/PET imaging

Find out their solution by reading the news story in Chemistry World and downloading Coogan’s ChemComm communication.

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MOF magnets deliver drugs

German scientists have encapsulated nanomagnets inside metal organic frameworks (MOFs). The MOF magnets can be filled with a drug, which is released when a magnetic field is applied. 

Stefan Kaskel from the Technical University of Dresden and colleagues made the MOF magnets by integrating superparamagnetic iron oxide particles into carboxylate MOFs. ‘Carboxylate molecules stabilise and activate the nanoparticles,’ explains team member Martin Lohe.

The group then loaded their MOF with ibuprofen and found that they were able to trigger and control its release by simply applying an external magnetic field. The magnetic field heats the magnets in the MOF, which causes the load to burst from the framework.

Superparamagnetic functionalisation of MOFs enables magnetic heating to trigger drug delivery

MOFs in which the frameworks themselves are magnetic have been made before, but they are not easy to manipulate. Kaskel’s embedded MOF magnets, however, can easily be manipulated from the outside. Magnetic fields can penetrate human skin, and magnetic triggers that could be used to release the drugs are already available on the market. However, before the MOF magnets can be used in the human body, toxicity tests will need to be done.

‘An enhanced sustainability of industrial and medical processes is crucial for our future,’ says Lohe. ‘Magnetically functionalised MOFs could be a small building block on this path.’

‘The particles will certainly increase the possibility of using nanoMOFs for drug delivery applications in the near future,’ agrees Christian Serre, an expert in porous solids from the University of Versailles  in France, ‘and they’ll add a new tool to the emerging domain of MOFs in biomedicine.’ 

Ruth Doherty

 

Link to ChemComm article

 Heating and separation using nanomagnet-functionalized metal–organic frameworks
Martin R. Lohe, Kristina Gedrich, Thomas Freudenberg, Emanuel Kockrick, Til Dellmann and Stefan Kaskel,

Chem. Commun., 2011, DOI: 10.1039/c0cc05278g

 

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Palladium impurites are not essential for gold catalysis

Spanish scientists have proved that gold alone can catalyse cross-coupling reactions, following a claim made last year that palladium impurities in the gold are essential for the catalysis. 

Avelino Corma from the Polytechnic University of Valencia and colleagues used kinetic and theoretical studies to prove that gold can catalyse the Sonogashira coupling reaction between phenylacetylene and iodobenzene. ‘Gold nanoparticles are active enough to promote the reaction, regardless of the presence or absence of palladium,’ says Corma.

Graphical abstract: Gold catalyzes the Sonogashira coupling reaction without the requirement of palladium impurities

Read the full news story in Chemistry World and download Corma’s ChemComm communication

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Novel concept for switchable olefin metathesis catalysts

Chemists have discovered a novel triggering mechanism for olefin metathesis catalysts while unravelling the mechanism of a crucial ligand rearrangement step.

Olefin metathesis is a widely used reaction in organic and polymer synthesis. cis Dichloro ruthenium benzylidene complexes bearing an N-heterocyclic carbene ligand have recently gained considerable attention as stable metathesis catalysts. They are known as latent catalysts as they initiate slowly, which is thought to be because the cis dichloro precursors have to rearrange to their trans dichloro counterparts to become active.

While studying the reaction mechanism, Christian Slugovc and colleagues at Graz University of Technology, Austria, discovered that a cationic complex is an intermediate in the rearrangement step. They also observed that pyridine, which is a donor ligand, facilitates the displacement of one of the chloride ligands, the first step in the rearrangement.

Graphical abstract: Pyridine as trigger for chloride isomerisation in chelated ruthenium benzylidene complexes: implications for olefin metathesis

But most striking, says Slugovc, is that the chloride counterion (or, more generally, a counterion that can coordinate to ruthenium) is indispensible for the catalytic activity. Changing the counterion for the non-coordinating hexafluorophosphate ion produced an almost inactive catalyst, but the activity was triggered again by adding chloride. Slugovc says this constitutes a novel concept for switchable olefin metathesis catalysts.

Download Slugovc’s ChemComm communication to find out more.

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