Chemical Science Blog

A team of researchers led by Takashi Nakanishi from the National Institute for Materials Science in Japan have made a nanocarbon hybrid of a C₆₀ derivative and single-walled carbon nanotube (SWCNT) to be used in photovoltaic devices.  The high performance of the nanomaterial is the result of a combination of the optical and electronic properties of the SWCNTs with the electron-accepting property of C₆₀.

Photoconductivity experiment using a field-effect transistor equipped with the carbon nanohybrid

The C₆₀ is decorated with long alkyl chains which have an affinity for the SWCNT surface, avoiding the problems associated with covalent functionalisation when combining such materials. By incorporating C₆₀ into the hybrid, the SWCNTs were soluble in organic solvents meaning classic wet processes can be used to fabricate the photovoltaic device.

The nanocarbon material also has the added benefit of being superhydrophobic, providing the device with waterproof properties.

 To find out more about this research, read the Chemical Science Edge article.

Scientists have found that the way ice bonds to metal does not obey the ‘ice rules’. Andrew Hodgson, together with teams from the UK and Spain, wanted to understand water–metal and hydroxyl–metal interactions, to devise molecular models of wet metal interfaces for studying catalytic and electrochemical reactions that occur on these types of surfaces.

Using scanning tunnelling microscopy and density functional theory calculations, the teams produced a phase diagram for water and hydroxyl on a copper surface, providing a complete molecular description of the complex hydrogen bonding structures formed. They saw three distinct phases as the temperature was decreased and the water/hydroxyl ratio increased: pure OH dimers, extended 1H₂O:1OH chains aligned along the close-packed Cu rows, and finally a distorted 2D hexagonal c(2 × 2) 2H₂O:1OH network.

Binding geometry and simulated STM images for (a) an isolated OH group, (b) an OH dimer and (c) an array of OH forming a dimer chain on the copper surface

None of these phases obey the conventional ‘ice rules’. Instead, their structures can be understood based on weak H donation by hydroxyl, which favours H-bonding structures dominated by water donation to hydroxyl, and competition between hydroxyl adsorption sites.

Found out more by downloading the Chemical Science Edge article.

A method for making modified RNA provides a new tool to study non-coding RNAs (functional RNA molecules not translated into a protein), say researchers from Germany and Austria.

Chemical synthesis of modified DNA and RNA is limited by size and by type of modification, so scientists are searching for new methods to overcome these limitations. To modify RNA, Ronald Micura and Andreas Marx and their teams used an enzyme – an RNA polymerase – rather than conventional synthesis methods.

To find out more, read the Edge article.

Researchers have shown that acid-catalysed condensations of aminobenzaldehydes with indole result in the formation of different products depending on whether the aminobenzaldehyde is primary or secondary.

Daniel Seidel’s group at Rutgers, The State University of New Jersey, found that N-methylbenzaldehyde reacts with indole to form neocryptolepine-related structures in a single step. Neocryptolepine (5) and its analogues are attractive targets for synthesis as they display promising antimalarial activity.

Conversely, primary benzaldehydes such as aminobenzaldehyde react under similar conditions to form quinolines (7). The mechanistic pathways leading to the formation of both indoles (5) and quinolines (7) are initially identical, with aminobenzaldehyde 1 condensing with indole 2 to form the corresponding azafulvenium ions (3), which undergo ring closure to yield tetracyclic products (4). At this point the mechanisms diverge; secondary systems (4a) undergo proton loss and oxidation to give neocryptolepine analogues (5), whilst primary systems (4b) undergo proton transfer to give products of type 6, which aromatise to form quinoline products (7) on ring opening.

The group made a range of both neocryptolepine analogues and quinoline systems in good to excellent yields, representing important scaffolds for medicinal chemistry.

Seidel’s Edge article is free to download. Let me know what you think of this work by leaving your comments below.

Posted on behalf of Alice E. Williamson, Chemical Science web writer.

Researchers from the University of Delaware have reported a total synthesis of hyacinthacine A2, an attractive target owing to its selective glycosidase inhibition and activity against HIV. 

Joseph Fox’s research group achieved the synthesis in less than ten steps from sucrose by designing and synthesising a functionalised 5-aza-cyclooctene system (1) that would undergo a novel transannular hydroamination, following stereocontrolled photoisomerisation.

The efficiency of the photoisomerisation process was improved by using a flow system that removes trans-isomers by selective complexation with silver salts, thereby enabling the cis-isomer of 1 to be recycled. Incorporation of a fused acetonide ring system in 1 imposed significant conformational constraints to favour formation of the desired trans-diastereosiomer 2 in good yield and in 8:1 diastereomeric ration following decomplexation from the silver salts.

Following separation of the major diasteroisomer of 2, and cleavage of both trifluoroacetyl and acetonide protecting groups, the corresponding ammonium salt was obtained. The planar chirality present in 2 was perfectly transferred in a transannular hydroamination to give the point chirality present in the natural product.

Find out more by downloading Professor Fox’s Chemical Science Edge article, which is free to access.

Posted on behalf of Alice E. Williamson, Chemical Science web writer.

Researchers in Australia have devised a new way to test how well drugs penetrate the low-oxygen core of solid tumours. ‘Hypoxic’ regions of tumours are notoriously difficult to target with drugs and the new work could help in the development of new compounds that can effectively reach these areas and efficiently kill the cells.

Tumours often grow faster than the blood vessels that supply them, and parts of the tumour therefore become starved of oxygen and grow slowly. This makes it difficult for drugs carried in the blood to reach these areas; furthermore many drugs rely on the rapid proliferation of cancer cells, so slowly growing ones are less susceptible.

One approach has been to develop ‘prodrugs’, which become toxic to the cell only upon entering the low-oxygen environment. Some of these are based upon cobalt(III) attached to a toxic ligand. In a hypoxic environment the cobalt is reduced to cobalt(II) and the ligand is released. However, there are currently no reliable ways either to visualise the hypoxic region of a tumour or to measure penetration of the drugs.

Now, Byung Kim, Trevor Hambley and Nicole Bryce at the University of Sydney have developed a three-dimensional model of a solid tumour with a hypoxic core that allows both the hypoxic region to be highlighted and the extent of penetration of prodrugs to be measured.