New micro-dendrites separate themselves from the field

Bioanalysis and biosensors represent a current area of wide interest in the chemical sciences. Much work is being put into methods that allow easy separation and detection of biological targets. Erkang Wang and coworkers at the Chinese Academy of Sciences in Changchun have presented a new way of doing just that.

The group synthesised a new type of silver micro-dendrite (SMD) that has a silver surface perfect for tethering biomolecules. The SMDs could also be reversibly separated and dispersed in water merely by oscillation and then settling under gravity for 30 seconds.

 

The team used the SMDs to successfully detect DNA from sickle cell disease, human T-lymphotropic virus and anthrax. Probe DNA was attached to the SMDs and then the target strands were selectively bound with a second, fluorophore-containing probe. The target DNA could then be detected using laser scanning confocal microscopy. They found that this technique was so sensitive it could even detect DNA with a one nucleotide mismatch.

Wang hopes that this type of separation system can be expanded to more targets and other types of sensing system.

Interested in finding out more? Then download the ChemComm article for free today and leave a comment below.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

ChemComm Symposium heads west…..

A 5am start was always going to be tough, particularly after such a successful event in Kyoto. That said, with cases packed, we headed to Kansai Airport…. next stop Beijing!

After a three hour flight, the ChemComm International delegation arrived at Beijing International Airport where we had a four hour layover. After lunch, we were joined by the RSC Publisher for China, Dr Daping Zhang, and Professor Keiji Maruoka, the final international speaker for the next two events. The flight to Lanzhou was smooth and, to our delight, we were met by the former director of the Key State Laboratory and member of the Chinese Academy of Sciences, Professor Yong-Qiang Tu. Following a buffet dinner accompanied by excellent regional red wine, the speakers retired early with one eye on the second symposium

The following morning, we were greeted at the entrance to Lanzhou University with possibly the largest ChemComm advertising sign I have ever seen. ‘Big’ was certainly the theme of the day, with Professor Wei Wang informing speakers that an audience of around 400 was anticipated with 80 posters to review over lunch.

Professor Tu opened events and chaired the first session, inviting Professor Xinhe Bao to the stage. Professor Bao gave a beautiful overview on some of his very detailed studies into heterogenous catalysis within nanotubes and other nano-confined systems. Using nobel metals or metals such as iron or nickel, it was shown that the conversation of syngas was much more efficient inside the tube than outside. The subject of the session then switched to metal-free homogenous catalysis, as Professor Maruoka spoke about some of his latest results in the field of organocatalysis. As you would expect, high enatiomeric excesses and yields were the order of the day.

 Following coffee, Professor Veronique Gouverneur gave another whistle-stop tour of her group’s latest organofluorine chemistry and the formation of  C–F bonds using palladium and gold homogenous catalysis.

As in Kyoto, the speakers worked hard over lunch analysing the 80 posters on show. They covered everything from organic methodology, to total synthesis, organic materials and supramolecular chemistry. If they thought judging them was tough in Kyoto, it proved even more so in Lanzhou! Unfortunately, Professor Ben Feringa was unable to act as a judge, because, due to a last minute laptop crisis, his presentation was being transferred to a spare laptop, with his own laptop in pieces, being fixed by helpful student Mr Woo.

After lunch, the conference switched gears to total synthesis. Professor Dawei Ma spoke first about the total synthesis of galbulimima alkaloids and communesins. Professor Ma was followed by Professor Viresh Rawal, who gave a different talk to that described in the programme. Professor Rawal described his recent total synthesis of Pederin and Mycalamide B, both part of the Pederin family of natural products isolated from the beetle Paederus fuscipas. He also introduced initial work looking at bioactivity of Mycalamide in cells, carried out with Milan Mrksich

For the final session, the audience were treated to a masterclass from Ben Feringa on molecular motors and switches. This was only made possible by Mr Woo, who had rebuilt his computer, replacing a transistor, and bingo! His synthetic motors, inspired by nature, are unidirectional with the direction controlled by the enantiomer used. By adding legs, the motors can be bound to gold surfaces and then used to change the orientation of liquid crystal films. A great talk and even Professor Bao, the session Chair, could not bring himself to cut it short. Thank goodness for Mr Woo! The final talk of the day was presented by Professor Deqing Zhang on tetrathiafulvalene-based switchable molecular systems towards functional materials. 

The evening social events were as memorable as the science, with the speakers joined by 50 or so guests including the vice Dean of Lanzhou University. The Chinese banquet was enhanced with locally produced red wine and Chinese liquor (only to be drunk in multiples of three – Chinese style…kambai). After many toasts and speeches, the speakers were taken to a local pub for some traditional Chinese music. The night was not done, however, as we then moved to a Tibetan bar. The speakers were told to expect local singing and dancing. Little did they know that they would be involved! After being sung to, each speaker was presented with a white Hada. What a great way to end such a action-packed day.

Next stop Tianjin for the final event of three…..

Robert Eagling

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Recyclable DABCO-based organocatalyst

Fluorous tagging of 1,4-diazabicyclo[2.2.2]octane (DABCO) through the halogen bond creates a recyclable organocatalyst for the Morita-Baylis-Hillman reaction, say scientists in France.
 

Fluorous tagging of DABCO through halogen bonding makes recyclable catalyst for well known organic reaction

Julien Legros and colleagues from the University of Paris-Sud, applied the fluorous tagging technique (often used in organometallic catalysis) to an organocatalyst, where the fluorous tags were ‘grafted’ in a supramolecular fashion through the halogen bond. The resulting catalyst is readily accessible and can be recovered using a simple precipitation and filtration method, allowing recyclability up to five times.

Fancy finding out more? Then download the ChemComm communication, which will be free to access until the 10th June 2011.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Supramolecular Chemistry—Introducing the latest web themed issue

Graphical abstract: Supramolecular Chemistry—Introducing the latest web themed issueChemComm issue 21 is now online and includes an Editorial from Philip Gale, Jonathan Sessler and Jonathan Steed, guest editors of the recent Supramolecular Chemistry web themed issue.

Featuring over 60 articles (and growing!), the web theme showcases a collection of cutting edge contributions by international leaders in the field of supramolecular chemistry to mark the International Year of Chemistry 2011.

Browse this exciting web theme today to read the latest urgent communications. You can also catch up on a decade’s worth of progress in supramolecular chemistry by reading the issue’s Highlights in Chemistry.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

The 5th ChemComm International Symposium gets underway….

The 5th International ChemComm Symposium got off to an excellent start in Kyoto, Japan, on Monday (16th May) under the Chairmanship of ChemComm Editorial Board member and distinguished Professor Keiji Maruoka (Kyoto University).

World leading authorities from the USA, UK, the Netherlands, China and Japan arrived on Sunday in time to be treated to a ten course western-style dinner. The dinner was a perfect start to proceedings but even the ten courses could not over-shadow the science that was to follow.

With an audience in excess of 100, I opened the symposium and thanked the local organisers, speakers and poster presenters. Special thanks were also given to Professor Maruoka for all his support in organising the event. As the first session Chair, Professor Maruoka then got things underway.

Professor Tsutomu Katsuki (Kyushu University) was up first, speaking initially about oxidation chemistry using ruthenium but then moving, like nature, to iron, for example. He was followed by Professor Kuiling Ding (Shanghai Institute of Organic Chemistry) who gave a talk of two halves, covering his group’s ongoing efforts to overcome the challenging issues in both homogenous and heterogeneous asymmetric catalysis.

A quick stop for refreshments was followed by Professor Véronique Gouverneur (University of Oxford) who spoke about her ongoing efforts to develop transition metal-catalysed reactions to generate C–F bonds. Not easy, but made even more challenging by the fact that the methods need to be incredibly quick so they can be used to incorporate hot [18F], which has a very short half-life. Such [18F] labelled compounds are used in positron emission tomography.

Ben Feringa discussed a posterOver lunch, the seven speakers interacted with the 35 poster presenters, putting them through their paces, with the five lucky winners scheduled to be announced at the end of the day.

The pace of the event did not slow after lunch. Professor Viresh Rawal (University of Chicago) wowed a packed auditorium with some of his latest results using H-bonded systems for asymmetric catalysis. Before the break, Professor Zhengfeng Xi (Peking University) spoke about the synthesis, unique reactivity, cooperative effect and applications of organo-di-lithio reagents.

The symposium was closed first by Professor Atsuhiro Osuka (Kyoto University), who spoke about some of his beautiful results in the area of Möbius porphrin chemistry, and then by Professor Ben Feringa (University of Groningen). Professor Feringa gave a wonderful overview of some of the ongoing research in his lab exploring chiral space in asymmetric catalysis. Some highlights included the latest examples of C–H and C–C bond formation using monodentate phosphoramidite ligands and also new results in the field of asymmetric catalysis using DNA with his colleague Professor Gerard Roelfes. The later certainly generated a number of interesting questions about the length and sequence requirements of the DNA involved in the reactions.

symposium speakers, poster prize winners and chairmanAfter the formal poster prize presentations, the speakers and organising committee were treated to a traditional Japanese meal. Before dinner, the historic nature of the Japanese tea ceremony was explained in detail and served to the group by a Maiko (a young training Geiko). Through dinner, the speakers were also treated to some traditional Japanese singing and dancing performed by the Maiko. The music and dance showcased the four seasons of Kyoto.

The dinner finished with the speakers retiring to bed in preparation for their early flight first to Beijing and then Lanzhou, the next venue for the second of three ChemComm symposia.

Robert Eagling

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Iron oxide mediated C-C bond formation

An efficient iron oxide catalysed cross-coupling reaction between organometallic species and cyclic ethers, via activation of C(sp3)-H, has been developed by scientists in India. This is the first example of iron oxide mediated direct C-C bond formation without expensive or toxic ligands.

Metal catalysed cross-coupling reactions for C-C bond formation via C-H activation is a hot topic in catalysis research at the moment. Many reactions via the activation of C(sp2)-H have been reported, but examples via C(sp3)-H activation remain much more elusive. 

Iron oxide mediated C-C bond formation

Ram Vishwakarma and colleagues at the Indian Institute of Integrative Medicine have cleverly devised a cross-coupling reaction that does exactly that. They found that reacting alkyl- and aryl-magnesium halides with tetrahydrofuran (and other cyclic ethers) via activation of the C(sp3)-H results in C-C bond formation. The method is inexpensive (thanks to the cheap iron catalyst) and no toxic ligands are used.

I’m sure you’ll agree, this is an interesting addition to a hot research area and leaves me wondering about the impact this will have in research laboratories across the globe.

Fancy knowing more about the reaction conditions and substrates used in this reaction? Then download the ChemComm communication, which will be free to access until the 10th June 2011.

You may also be interested to know that Chemical Society Reviews recently published a themed issue on “C-H functionalisation in organic synthesis” guest edited by Huw M. L. Davies, Justin Du Bois and Jin-Quan Yu.
Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

A new twist on fluorescent labelling proteins

Incorporating a small fluorophore allows protein folding and redox states to be monitored

Labelling site for the atpt iodoacetamide structure

A new thiol-specific reagent can introduce a small bis(methylamino)terephthalic acid fluorophore into proteins. The noninvasive probe has distinct spectroscopic properties and can offer many advantages towards protein labelling, purification, and mechanistic work. Ekaterina Pletneva and her team at Dartmouth College in the US believe that this complex promises to serve as a powerful tool when it comes to studying protein folding and heme redox reactions.

 Did you find this result exciting? Then download the ChemComm communication to find out more. The article will be free to access until the 10th June 2011.

 

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

The first use of organometallic hosts in crystalline organic frameworks

Chemists working at Ruhr-University Bochum in Germany have for the first time studied the host–guest chemistry of organometallic complexes with covalent organic frameworks (COVs).

COVs are the organic analogues of metal–organic frameworks (MOFs) and are made up of strong organic covalent bonds to form large organic polymers. They have a crystalline  structure and have attracted a lot of attention due to their possible applications in gas storage, sensing and catalysis. To date, only the  host–guest chemistry of small gas molecules such as CO2 and H2 have been studied in COVs. The team in Germany, led by Roland A. Fischer, set about changing this and demonstrated the use of organometallic molecules as guests.

Using COF-102 as the host, the team looked at the adsorption of FeCp2 , CoCp2 and [Ru(cod)(cot)] within the framework. They found that FeCp2 remained intact within the framework and that it assumed a structure reminscent of the host via π–π interactions.  Overall, the work displayed the similarity between COVs and MOFS as hosts for metal complexes.

If you are interested in finding out more on this hot area then why not download the full ChemComm article for free today?

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

The inhibition effect of Naringenin

With the help of two single-molecule techniques, the inhibitor effects of Naringenin become apparent

Chinese scientists have confirmed that Naringenin inhibits transforming growth factor-β (TGF-β) signaling in living cells.

Naringenin is a natural predominant flavanone with many pharmacology activities

TGF-β signalling plays a crucial role in a wide variety of biological processes, such as cell growth, differentiation, apoptosis, and embryonic development. Xiaohong Fang and colleagues from the Chinese Academy of Sciences, in Beijing, and co-workers from nearby Peking University, believe that developing TGF-β signalling inhibitors will help create new therapeutic reagents and anticancer drugs of the future. Here, Fang and his team have shown that Naringenin, a natural flavonone, inhibits this important signalling receptor, evidence supported by single-molecule fluorescence microscopy and single molecule force spectroscopy techniques.

Fancy reading about the techniques used, or finding out more on the inhibition mechanism? Then download the ChemComm communication, which is free to access until the 3rd June 2011!

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

To expand or not to expand?

Find out how 10 degrees can make all the difference for dumbell-shaped polymorphs

Two dumbbell-shaped polymorphs possess similar packing arrangements, but one shows anomalously anisotropic thermal expansion while the other does not.

Leonard J. Barbour and his team from the University of Stellenbosch, in South Africa and a co-worker from the Polish Academy of Sciences, have investigated these polymorphs further and discovered that by adjusting the molecular stacking angle by approximately 10° effectively disables the molecules’ ability to undergo thermal expansion.

Fancy expanding your knowledge? Then why not download the ChemComm communication today and read all about the teams research results? This article is free to access until Friday 3rd June.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)