Archive for April, 2011

Top ten most accessed articles in March

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

Porous metal-organic frameworks as platforms for functional applications 
Hai-Long Jiang and Qiang Xu 
Chem. Commun., 2011, 47, 3351-3370, DOI: 10.1039/C0CC05419D, Feature Article 

Surface modification of polyoxometalate host-guest supramolecular architectures: from metal-organic pseudorotaxane framework to molecular box 
Xiaofei Kuang, Xiao-Yuan Wu, Jian Zhang and Can-Zhong Lu 
Chem. Commun., 2011, 47, 4150-4152, DOI: 10.1039/C0CC05855F, Communication 

Homogeneous catalysis using iron complexes: recent developments in selective reductions 
Kathrin Junge, Kristin Schröder and Matthias Beller 
Chem. Commun., 2011, 47, 4849-4859, DOI: 10.1039/C0CC05733A, Highlight 

How easy are the syntheses of allenes? 
Shichao Yu and Shengming Ma 
Chem. Commun., 2011, 47, 5384-5418, DOI: 10.1039/C0CC05640E, Feature Article 

Fe3O4 nanostructures: synthesis, growth mechanism, properties and applications 
Ce Yang, Jiajia Wu and Yanglong Hou 
Chem. Commun., 2011, 47, 5130-5141, DOI: 10.1039/C0CC05862A, Feature Article 

Ordered mesoporous materials as adsorbents 
Zhangxiong Wu and Dongyuan Zhao 
Chem. Commun., 2011, 47, 3332-3338, DOI: 10.1039/C0CC04909C, Highlight 

Mn12 single-molecule magnet aggregates as magnetic resonance imaging contrast agents 
Yinglin Wang, Wen Li, Shengyan Zhou, Daliang Kong, Haishan Yang and Lixin Wu 
Chem. Commun., 2011, 47, 3541-3543, DOI: 10.1039/C0CC03758C, Communication 

A Covalent Organic Framework with 4 nm open pores 
Mirjam Dogru, Andreas Sonnauer, Andrei Gavryushin, Paul Knochel and Thomas Bein 
Chem. Commun., 2011, 47, 1707-1709, DOI: 10.1039/C0CC03792C, Communication 

Selective CO2 adsorption in a flexible non-interpenetrated metal-organic framework 
Tae Kyung Kim and Myunghyun Paik Suh 
Chem. Commun., 2011, 47, 4258-4260, DOI: 10.1039/C0CC05199C, Communication 

A colorimetric and fluorescent chemosensor for the detection of an explosive-2,4,6-trinitrophenol (TNP) 
Yu Peng, Ai-Jiang Zhang, Ming Dong and Ya-Wen Wang 
Chem. Commun., 2011, 47, 4505-4507, DOI: 10.1039/C1CC10400D, Communication 

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

Fancy submitting an article to ChemComm? Then why not submit to us today or alternatively contact us with your suggestions.

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Antonio Echavarren joins the ChemComm Editorial Board

Antonio EchavarrenOn behalf of the ChemComm Editorial Board, I am delighted to welcome Professor Antonio Echavarren as the new ChemComm Associate Editor for organic chemistry and catalysis.

Professor Echavarren is Group Leader at the Institute of Chemical Research of Catalonia (ICIQ) in Tarragona, Spain. His research focuses on developing new catalytic methods based on the organometallic chemistry of transition metals as well as synthesing natural products and polyarenes.

Professor Echavarren’s editorial office is now open for submissions, welcoming urgent communications highlighting the latest advances in organic chemistry and catalysis.

Find out more about Professor Echavarren’s research on gold catalysis by reading these exciting articles:

A multipurpose gold(I) precatalyst
Mihai Raducan, Carles Rodríguez-Escrich, Xacobe C. Cambeiro, Eduardo C. Escudero-Adán, Miquel A. Pericàs and Antonio M. Echavarren, Chem. Commun., 2011, 47, 4893-4895

Mechanism of the gold-catalyzed cyclopropanation of alkenes with 1,6-enynes
Patricia Pérez-Galán, Elena Herrero-Gómez, Daniel T. Hog, Nolwenn J. A. Martin, Feliu Maseras and Antonio M. Echavarren, Chem. Sci., 2011, 2, 141-149

Are you an organic chemist based in North America? Submit your research to Michael Krische, ChemComm North American Associate Editor for organic chemistry.

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Antibody acts as rudder to steer DNA into a pore

Scientists from China and Canada have studied the effect of a DNA-binding antigen-binding fragment (Fab) of an antibody on the translocation of a DNA polymer. Both poly(dT)45:Fab HED10 and poly(dT)45 produce unique double step current traces, which were analysed in detail to get information about the translocation events.

Representation of an α-HL pore and the mechanism for the poly(dT)45 specific binding with Fab HED10. A biological α-HL nanopore is embedded in a lipid bilayer. The narrowest section of α-HL is 1.4 nm. The potential across the bilayer membrane is applied through Ag/AgCl electrodes. In 10 mM Tris-HCl (pH = 7.8) buffer, the antibody recognizes four consecutive thymine residues of poly(dT)45.

The results have important implications for understanding the translocation behaviour of polymers, which could help to develop nanopore biosensors with high sensitivity and specificity, says Yitao Long, from East China University of Science and Technology. In particular, the addition of polymer-binding antibodies may facilitate the use of nanopores in sequencing technologies.

The presence of the FAB HED10 decreases the time of the first level of the step but not the second. The Fab appears to behave as a rudder, which significantly decreases the energy barrier for poly(dT)45 translocation. A more rigid or extended conformation of poly(dT)45 would decrease the time required to find the entrance to the narrow constriction in the pore. The entropic barrier required to linearise the DNA strand may be the dominant contribution to the entire energy barrier.

Find out more by downloading the communication, recently published in ChemComm.

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A touch of gold for cycloisomerisation reaction

Gold-catalysed cycloisomerisation of alkynyl hydroxyallyl tosylamides has led to the concise synthesis of oxaazatricyclic compounds and revealed an interesting skeleton structure, say scientists in South Korea.

Research groups across the globe have reported cycloisomerisation reactions of alkynyl allyl alcohols (AAAs) with rhodium, iridium, palladium and nickel catalysts. Naturally, research groups have been led into investigating the use of gold catalysts, providing plausible reaction pathways for these reactions. 

Young Keun Chung and colleagues from Seoul National University and Sangmyung University, used subtly different reaction conditions than have been previously reported, resulting in an usual oxaazatricyclic skeleton compound being uncovered for the first time, as shown in the X-ray structure obtained below.

X-ray structure of cycloisomerised oxaazatricyclic compound

To find out more about this unexpected result and the reaction conditions used, why not download the communication today? The results have been published in ChemComm and will be freely available until the 13th May 2011!

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Unique sorption properties for isomeric frameworks

Two porous supramolecular isomeric frameworks have shown unique sorption properties, say a collaboration of Chinese and Japanese scientists. 

One framework shows temperature dependent and selective sorption of CO2, while the other framework shows gas uptake capacity for CO2, N2, H2 and CH4 at low temperature and selective sorption of CO2 over N2 around room temperature. Wei-Yin Sun and colleagues believe that the results provide useful guidance for improving metal organic framework (MOF) designs for gas storage and separation techniques. 

 

Two porous supramolecular isomeric frameworks show unique sorption properties

Find out more, by reading the research results published in ChemComm. This article has been made free to access until the 13th May 2011, so why not download the communication today? 

  

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All systems GO for biosensing platform

Graphene oxide (GO) plays a crucial role in a new, sensitive biosensing platform, acting as an efficient quencher for upconversion nanophosphors, say scientists in China. 

Zhengping Li, Chenghui Liu and colleagues from Hebei University, have constructed a sensitive and practical biosensing platform by combining lanthanide-doped upconversion nanoparticles (UCNPs) with single-stranded DNA (ssDNA). Upon the addition of water soluble GO the upconversion fluorescence is quenched, effectively turning ‘off’ the fluorescence signal. To test the platforms sensing ability and performance, the team introduced adenosine triphosphate (ATP) resulting in the formation of an aptamer-ATP complex, preventing the UCNPs interacting with the GO surface and thus decreasing the quenching efficiency, resulting in the fluorescence staying ‘on’. Other phosphates were tested, like guanosine triphosphate (GTP), cytidine triphosphate (CTP) and uridine triphosphate (UTP) but no dramatic fluorescence enhancement was observed, so this indicates that the aptamer system is specific to ATP alone.

Upconversion FRET between ssDNA-UCNPs and GO for ATP sensing

Interestingly, the team also tested the biosensing platform with mercury ions, which caused the ssDNA to form double-stranded DNA (dsDNA), preventing the UCNPs interacting with the GO surface and again resulted in enhanced fluorescence emission. Other similar cations were tested in comparison, but the biosensor only shows selectivity for mercury ions, providing a good indication into the high specificity that this biosensing platform has, in addition to its future potential for uses in clinical diagnostic and biosensing applications.

Fancy finding out more? Then why not download the communication today – published in ChemComm, the article has been made free to access until the 13th May 2011.

Please also let us know what you think to this research by blogging some comments below.

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A new and simple polymer synthesis for polymer solar cells

A team of Swedish chemists have presented a novel and straightforward method for synthesising polymers for use in polymer solar cells (PSC) with a wide absorption spectrum.

The researchers, led by Mats R. Andersson from the Chalmers University of Technology in Sweden, synthesised the polymer from a widely available stannyl thiophene and an easily synthesised bromoisoindigo monomer. These were then coupled together using a Stille coupling reaction. Overall this represents just 3 steps and was achieved with a high overall yield of 68%.

 

The polymer itself is a low band-gap polymer with a donor–acceptor structure, which is important for harvesting photons from sunlight. The team found that the polymer exhibited promising performance when used in a PSC device and expect to be able to further improve this by varying the indigo groups.

If you would like to read more about this topic then download the ChemComm article for free today. Also, why not check out these other great ChemComm articles on PCSs?

Synthesis of annulated thiophene perylene bisimide analogues: their applications to bulk heterojunction organic solar cells
Hyunbong Choi, Sanghyun Paek, Juman Song, Chulwoo Kim, Nara Cho and Jaejung Ko
Chem. Commun., 2011, DOI: 10.1039/C0CC05448H

Crystalline conjugated polymer containing fused 2,5-di(thiophen-2-yl)thieno[2,3-b]thiophene and thieno[3,4-c]pyrrole-4,6-dione units for bulk heterojunction solar cells
Guan-Yu Chen, Yu-Hsin Cheng, Yi-Jen Chou, Ming-Shin Su, Chia-Min Chen and Kung-Hwa Wei
Chem. Commun., 2011, DOI: 10.1039/C1CC10585J

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Reusable template for pattern transfer

Contact area lithography has been used for directly patterning and transferring self-assembled monolayers (SAMs) onto silicon-based substrates.

 

One-step patterning & transfer of SAMs on SiO2/Si substrates

Hyunjung Shin and colleagues from Kookmin University, in South Korea used a patterned (hard) silicon oxide template and placed it on substrates of interest, introducing a small amount of water in the process.
After drying off the water, the non-contacted areas served directly as growth sites of OTS-SAMs by simple solution deposition. The hard template was then detached from the substrate and the patterns of SAMs were obtained.

In principal, the hard template is cleansable by simple chemical etching without causing any damage. It is also 100% recyclable and can be reused up to ~50 times.

Fancy finding out more about this technique? Then why not download the communication today, which has been published in ChemComm and will be free to access until the 13th May 2011.

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Beads clicking into place

Scientists in Belgium have designed a microfluidic setup that manufactures thiol and yne beads, which can then undergo several click-type reactions.

Filip Du Prez and his team at Ghent University demonstrated the yne beads reacting with an azide or two thiols, whereas the thiol beads were tested using nine different reaction conditions. The thiol–isocyanate reaction was seen to be the fastest, being closely followed by the thiol–norbornene reaction.

 

Light Microscopy image of monodisperse thiol beads (left image). Fluorescent yne beads after clicking with coumarin-derivative (right image).

Du Prez believes that this discovery may help to guide researchers, especially in the field of solid phase synthesis, to choose the most suitable ligation reaction according to their needs since many of the conjugations studied are part of the click family. 

Published in ChemComm this communication will be freely available until the 13th May 2011. Why not download the communication today and find out more about the beads and their clicking abilities?

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A rare example of synthon polymorphism

Scientists in India have reported a rare example of synthon polymorphism in co-crystals of 4,4′-bipyridine and 4-hydroxybenzoic acid.

Graphical abstract: Synthon polymorphism and pseudopolymorphism in co-crystals. The 4,4′-bipyridine–4-hydroxybenzoic acid structural landscape

Polymorphism is defined as the ability of a material to exist in more than one form or crystal structure. It has important implications for the properties of such materials; for example in pharmaceuticals, the dissolution rate of a drug can be dependent on the polymorphic form. While this is a common phenomenon in single crystals it is much less common in co-crystals, systems where the structure has at least two distinct components.

Gautam Desiraju from the Indian Institute of Science, found that when 4,4′-bipyridine and 4-hydroxybenzoic acid were dissolved together in a solvent such as methanol they would co-crystallise to form two different polymorphs. They noticed that a third form, a pseudopolymorph, was also present.

If you would like to read more about Desiraju’s discovery then why not download his ChemComm article for free today? This article is also part the ChemComm web themed issue on Supramolecular Chemistry to mark the International Year of Chemistry 2011.

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