Theoretical trinorbornane joins the real world

Scientists have successfully synthesised one of last small polycyclic hydrocarbons left to make or find in nature.1

Until recently, trinorborane (tetracyclo[5.2.2.01,6.04,9]undecane) had only existed in the Chemical Universe Database (GDB) – a database containing all possible molecules up to a certain number of atoms.2 Trinorbornane has an interesting structure where two norbornanes share a pair of neighbouring edges so it looks like three interlaced norbornanes.

Source: Royal Society of Chemistry
The two enantiomers of trinorbornane display axial chirality

Read the full story by Adrian Robinson on Chemistry World.

1 L D Bizzini et al, Chem. Commun., 2017, DOI: 10.1039/c7cc06273g (This paper is free to access until 16 November 2017.)

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Synthesis of Tin Dioxide Nanotubes for Lithium-ion Batteries with “A Grain of Oxalate Salt”

Preparation of tube-shaped electrode materials for lithium-ion batteries is a trending topic. Tubes with hollow cylindrical bodies allow exposure of the electrodes’ interior surface and can accommodate the large volumetric expansion commonly observed when lithium ions diffuse (either via intercalation or alloying) into the electrodes. The aforementioned two characteristics improve the specific capacity (a measure of how much electric energy one electrode can hold) and lifetime of electrodes.

Recently, the Mai research group from Wuhan University of Technology, China demonstrated a straightforward method for the synthesis of tin dioxide nanotubes as high-performance anodes for lithium-ion batteries. They adopted manganese(III) oxyhydroxide (MnOOH) nanowires as the sacrificial templates and immersed them in a batch of aqueous solutions containing tin(II) cations and oxalate anions (C2O42-). Afterwards, they warmed the mixture at 60 oC under constant magnetic stirring for 4 h and collected a white precipitate consisting of tin dioxide nanotubes. These nanotubes were then washed and coated with carbon thin films to improve their electrical conductivity and structural stability before being subjected to performance evaluations.

The presence of oxalate anions was crucial for producing the nanotubes with a well-defined shape. The function of these anions was revealed through a series of experiments. Oxalate anions first reduced MnOOH to manganese(II) cations and consumed protons in the vicinity of the MnOOH surface. The consumption of local protons increased the local pH and triggered precipitation and oxidation (by dissolved oxygen) of Sn2+ to tin dioxide. The two reactions proceeded, and eventually the MnOOH nanowires disappeared but tubes of tin dioxide formed around their surfaces (Figure 1). Samples obtained without oxalate salts were irregularly shaped.

Figure 1. (a) The schematic illustration of the synthesis steps of the tin dioxide nanotubes. (b) Scanning electron microscopy and (c) transmission electron microscopy images of the as-prepared tin dioxide nanotubes.

The carbon-coated tin dioxide nanotubes showed superior stability performance to bare tin dioxide nanotubes, as shown from the slower capacity-fading rate depicted in Figure 2a. In addition, carbon coating did not significantly sacrifice nanotubes’ charge-storage performance as both electrodes with and without a coating exhibited comparable capacity at all tested current densities (Figure 2b).

Figure 2. Performance comparison between carbon-coated tin dioxide nanotubes (SnO2@C NTs) and bare tin dioxide nanotubes (SnO2 NTs): (a) long-term stability and (b) capacity achieved at different current densities and charge-discharge cycle numbers.

To find out more please read:

Oxalate-assisted Formation of Uniform Carbon-confined SnO2 Nanotubes with Enhanced Lithium Storage

Chunhua Han, Baoxuan Zhang, Kangning Zhao, Jiashen Meng, Qiu He, Pan He, Wei Yang, Qi Li and Liqiang Mai

DOI: 10.1039/c7cc05406h

About the blogger:

Tianyu Liu is a Ph.D. in chemistry graduated from University of California, Santa Cruz in United States. He is passionate about scientific communication to introduce cutting-edge researches to both the general public and the scientists with diverse research expertise. He is a web blogger for the Chem. Commun. and Chem. Sci. blog websites. More information about him can be found at http://liutianyuresearch.weebly.com/.

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Carbohydrates promoted in new prebiotic theory

It’s plausible that carbohydrates formed on primordial Earth before amino acids. So say UK researchers who have shown that parent molecules to amino acids can catalyse the formation of 2-deoxy-D-ribose, a sugar found in the backbone of DNA.1

Source: Royal Society of Chemistry Amino nitriles can promote the enantioselective aldol reaction of formaldehyde and glycolaldehyde to yield D-glyceraldehyde, and the subsequent reaction of the D-glyceraldehyde with acetaldehyde to make 2-deoxy-D-ribose

We’ll never know the exact process that turned chemistry into biology, but many researchers want to get as close as they can to the truth. Paul Clarke at the University of York is one of those researchers.

Read the full story by Jennifer Newton on Chemistry World.

1 A M Steer et al, Chem. Commun., 2017, DOI: 10.1039/c7cc06083a (This paper is open access.)

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Let single crystals do the heavy lifting

Researchers in the US have developed heat responsive crystalline cantilevers that are capable of lifting a metal ball almost 100 times heavier than the crystal itself.

Stimuli responsive behaviour in soft materials has blossomed in recent years, but for highly crystalline solids, such properties are still surprising, especially for materials that don’t lose their single crystalline nature in the process.

Source: Royal Society of Chemistry
Upon heating, the crystal lattice changes from herringbone packing to infinite 1D chains stacked co-facially along their π surfaces.

Jeremiah Gassensmith and colleagues at the University of Texas at Dallas and the University of North Texas, US, have developed single crystals of an N-substituted naphthalene diimide (NDI) derived organic semiconductor that can undergo a reversible phase change from its α to its β form under heating.

Read the full story by Jason Woolford on Chemistry World.

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HOT ChemComm articles for August

All of the referee-recommended articles below are free to access until 6th October 2017.

Photoactivatable aggregation-induced emission of triphenylmethanol
Yue Zheng, Xiaokun Zheng, Yu Xianga and Aijun Tong
Chem.Commun., 2017, Advance Article
DOI: 10.1039/C7CC04693F, Communication

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Orthogonal switching of self-sorting processes in a stimuli-responsive library of cucurbit[8]uril complexes
Stefan Schoder and Christoph A. Schalley
Chem. Commun., 2017, 53, 9546-9549
DOI: 10.1039/C7CC05469F, Communication

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Condensing the information in DNA with double-headed nucleotides 
Mick Hornum, Pawan K. Sharma, Charlotte Reslow-Jacobsen, Pawan Kumar, Michael Petersena and Poul Nielsen
Chem. Commun., 2017,53, 9717-9720
DOI: 10.1039/C7CC05047J, Communication

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High magnetic relaxivity in a fluorescent CdSe/CdS/ZnS quantum dot functionalized with MRI contrast molecules 
S. G. McAdams, D. J. Lewis, P. D. McNaughter, E. A. Lewis, S. J. Haigh, P. O’Brien and F. Tuna
Chem. Commun., 2017, Advance Article
DOI: 10.1039/C7CC05537D, Communication
This article is part of the themed collection: Commemorating Michael Faraday (1791-1867)

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What [plasma used for growing] diamond can shine like flame?
Michael N. R. Ashfold, Edward J. D. Mahoney, Sohail Mushtaq, Benjamin S. Truscotta and Yuri A. Mankelevich
Chem. Commun., 2017, Advance Article
DOI: 10.1039/C7CC05568D, Feature Article
This article is part of the themed collection: Commemorating Michael Faraday (1791-1867)

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Reversible structural switching of a metal-organic framework by photoirradiation
Varvara I. Nikolayenko, Simon A. Herberta and Leonard J. Barbour
Chem. Commun., 2017, Advance Article
10.1039/C7CC06074B, Communication

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2nd From Carbon-Rich Molecules to Carbon-Based Materials Conference

The 2nd From Carbon-Rich Molecules to Carbon-Based Materials Conference is to be held 7th – 10th June in Nassau, Bahamas.

This interdisciplinary conference will provide unique “fusion” opportunities for chemists, physicists and engineers having various backgrounds but sharing passion and interests in carbon-only or carbon-rich molecules and carbon-based materials. It will allow a diverse group of scientists from all over the globe to discuss the current challenges, needs and prospects of this quickly-evolving multidisciplinary field.

Dates for your diary

Early Bird- 7th December 2017

Talk Submission- 14th December 2017

Last Chance – 13th April 2018

You can click here to register now and see here for further information about the conference.

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Janus Particle Chains that Can Rotate, Dissipate and Recombine

Janus is a god in ancient Roman mythology with two opposing faces. Its name has been brought to materials science to label particles with two or more distinct faces as “Janus particles”. Integrating multiple functions into one physical entity, Janus particles with various properties are extensively adopted as catalysts, electronic components and other applications.

Reporting in Chemical Communications, Bart Jan Ravoo and co-workers from Westfälische Wilhelms-Universität Münster in Germany developed a Janus particle colloidal assembly using a sandwich micro-contact printing method, a strategy reported previously by the same group. The Janus particle assembly consists of Janus particle chains, with the structure of one chain illustrated in Figure 1b. The authors first capped a batch of silica micro-beads with tri-block co-polymers on opposing ends (green parts shown in Figure 1). These copolymers serve as arms that extend and attach to functionalized magnetite (Fe3O4) nanoparticles. Two Janus particles will become magnetically glued together if they connect to the same nanoparticle at the two caps. This connection propagates and eventually forms Janus particle chains mainly consisting of two to four particles.

Figure 1. The schematic illustration depicting the structure of a Janus particle chain.

The artificial chains are responsive to an external magnetic field and photons with different wavelengths. Owing to the magnetic nanoparticles, the chains tend to arrange themselves according to the direction of the applied magnetic field. As shown in Figure 2a, the authors successfully rotated a chain by moving around a magnet.

Moreover, radiating the chains using UV light and green visible light will alter the chain configuration. The light sensitivity is rooted in a light-induced isomerization reaction of the co-polymer linkers: green light yields adhesive trans-isomers, whereas UV light produces cis-isomers that detach from magnetite. Hence, dissipation of the chains into individual Janus particles and then rejoining the particles together can be readily accomplished (Figure 2b).

Figure 2. Optical microscopy images showing (a) the magnetic and (b) the photo-switching properties of one Janus particle chain. All scale bars are 10 µm.

The demonstrated assembly is just the tip of the iceberg for Janus particle assemblies. As claimed by the authors, any acrylate in principal can be used to build the co-polymer linkers, resulting in colloidal assemblies with versatile features.

To find out more please read:

Self-assembly of Colloidal Molecules that Respond to Light and a Magnetic Field

Sven Sagebiel, Lucas Stricker, Sabrina Engel and Bart Jan Ravoo

DOI: 10.1039/c7cc04594h

About the blogger:

Tianyu Liu is a Ph.D. in chemistry graduated from University of California-Santa Cruz. He is passionate about scientific communication to introduce cutting-edge researches to both the general public and the scientists with diverse research expertise. He is a web writer for the Chem. Commun. and Chem. Sci. blog websites. More information about him can be found here.

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Fluorescent test strip detects deadly phosgene gas

Chinese scientists have improved the sensitivity of test strips for phosgene gas by using a different fluorophore.

Phosgene gas reacts with lung proteins, disrupting the blood–air barrier and suffocating victims. Although deadly, many chemical plants require phosgene to synthesise products such as pharmaceuticals and pesticides. But accidental leaks are a risk. In 2016, for example, a leak at Gujarat Narmada Valley Fertilizers and Chemicals in India killed four workers and affected nine others.

Source: Royal Society of Chemistry
This is the first test-strip sensing system for gaseous phosgene made with AIE-based fluorophores

 

Read the full story by Sarah Piggott on Chemistry World.

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Automated synthesis yields sugar high

An automated synthetic method designed by chemists in Germany has assembled the longest synthetic oligosaccharide ever made from monosaccharides. The method could help to up the pace of carbohydrate research by improving researchers’ access to synthetic glycans.

Source: © Royal Society of Chemistry The researchers used automated glycan assembly to make a 50mer polymannoside

Read the full article by Jennifer Newton on Chemistry World.

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Elucidating the Stability of Two Metal-Organic Frameworks toward Carbon Dioxide Sorption: A Comparative Study

Metal-organic frameworks (MOFs) are coordination networks consisting of organic ligands and metal cores. They possess crystalline structures with metal complexes as the basic building blocks. These complexes assemble together and extend periodically to form the MOF structures. MOFs represent a family of highly porous materials with ultrahigh surface area (typically >1000 m2 g-1). Other attractive characteristics for MOFs are abundant active metal cores and unique porous structures with tunable pore width, useful for gas storage applications.

Capturing carbon dioxide has evolved into an intriguing research area, mainly due to environmental concerns triggered by high levels of greenhouse gas emissions. Some MOFs have already been explored as carbon dioxide storage materials and exhibited storage capability exceeding that of conventional absorbents (e.g. amines). Aside from the absorption capacity of carbon dioxide, the performance stability over prolonged operation periods is another figure of merit for MOF-based absorbents. However, there are limited studies in this area. Now for the first time, research groups led by Zeng and Zhao from National University of Singapore compared the performance stability of two representative MOFs, HKUST-1 and UiO-66(Zr). The unit cell of the two MOFs are shown in the inset of Figure a.

The two aforementioned MOFs were subjected to 500 carbon dioxide absorbing and desorbing cycles (Figure a). The carbon dioxide uptake amount of the two MOFs was gauged at specific cycle numbers (Figure b). Whilst HKUST-1 displayed a consistent decreasing storage capacity with increasing cycle number, the capacity of UiO-66(Zr) fluctuated but remained relatively constant. The results clearly indicate that HKUST-1 is more vulnerable and instable than UiO-66(Zr) during long-term working cycles.

The authors then investigated the mechanisms associated with the different stability performances. They first observed that the surface area of HKUST-1 decreased 24% to 1270 m2 g-1 after the stability test, whereas that of UiO-66(Zr) remained relatively intact. Moisture-induced structural collapse was excluded as a possible reason by carrying out a control experiment with ultra-pure and dry hydrogen gas. The authors then exploited multi-frequency atomic force microscopy and concluded that the difference in elastic modulus of the two MOF crystals played an important role in determining the corresponding MOF durability. UiO-66(Zr) has an elastic modulus (ca. 28 GPa) much higher than that of HKUST-1 (ca. 19 GPa), meaning that the former is more elastic than the latter. The high elasticity of UiO-66(Zr) can efficiently buffer the volumetric deformation caused by carbon dioxide absorption and desorption, preventing UiO-66(Zr) crystals from structural failure.

Figure. (a) Illustration of one cycle of the carbon dioxide absorption-desorption test. The inset shows where one carbon dioxide molecule resides in the corresponding MOFs. (b) The evolution of carbon dioxide uptake capacity (blue) and surface area (black) of HKUST-1 and UiO-66(Zr).

This work is expected to provide general guidelines on studying the structural stability of other MOFs with applications associated with gas storage and separation.

 

To find out more please read:

Structure Failure Resistance of Metal-organic Frameworks toward Multiple-cycle CO2 Sorption

Zhigang Hu, Yao Sun, Kaiyang Zeng, and Dan Zhao

DOI: 10.1039/c7cc04313a

About the author:

Tianyu Liu is a Ph.D. in chemistry graduated from University of California-Santa Cruz. He is passionate about scientific communication to introduce cutting-edge researches to both the general public and the scientists with diverse research expertise. He is a web writer for the Chem. Commun. and Chem. Sci. blog websites. More information about him can be found at http://liutianyuresearch.weebly.com/.

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