Announcing the ChemComm Emerging Investigators issue 2014

Profiling the very best research from scientists in the early stages of their independent careers

Following the overwhelming postive response from the community to the 2011, 2012 and 2013 ChemComm Emerging Investigators issues, we are delighted to announce the forthcoming 2014 Emerging Investigators issue.

If you are interested in submitting to the issue please contact the ChemComm Editorial Office in the first instance. Please note that authors must not have featured in a previous ChemComm Emerging Investigators issue. The deadline for submission is 1 October 2013.

This annual 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.

Browse the 2013 Emerging Investigators issue

Find out more about the ChemComm Emerging Investigator Lectureship – awarded annually to exceptional scientists in the early-stage of their independent career

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ChemComm-RSC Prizes and Awards Symposium: Supramolecular Chemistry

Last month we were delighted to hold a ChemComm-RSC Prizes and Awards Symposium on supramolecular chemistry at Trinity College Dublin, Ireland. The free one-day event was a great success, with over 160 delegates and a fantastic programme featuring RSC Award winners and leaders in the field.

CC supramolecular symposium

Speakers from the ChemComm-RSC Prizes and Awards Symposium on Supramolecular Chemistry, 24 May 2013, Dublin, Ireland

Speakers included:

  • Jerry Atwood, University of Missouri-Columbia – Winner of the 2012 RSC Supramolecular Award
  • John Callan, University of Ulster
  • Chris Chang, University of California, Berkeley – Winner of the 2012 RSC Chemistry of Transition Metals Award
  • Sylvia Draper, Trinity College Dublin
  • Phil Gale, University of Southampton – ChemComm sponsored lecture
  • David Leigh, University of Manchester – ChemComm sponsored lecture
  • Donal O’Shea, University College Dublin
  • Susan Quinn, University College Dublin
  • Eoin Scanlon, Trinity College Dublin
  • Jonathan Steed, Durham University – ChemComm sponsored lecture

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Corporals can overrule Sergeants in self assembly

Creating chiral layers on a surface is attracting increased attention because of possible application in optical resolution and heterogeneous catalysis.  Chiral layers can be achieved by the self assembly of enantiopure molecules on a surface.

Alternatively, achiral molecules can be forced to form chiral surface assemblies by using a chiral building block or by adding a small amount of a chiral auxillary– the “Sergeant-and-Soldiers” effect first described by Mark Green (NYU-Poly) and co-workers in 1989.

In this HOT ChemComm article, Chem Soc Rev Associate Editor David Amabilino from ICMAB-CSIC, Barcelona, ChemComm Associate Editor Steven De Feyter from KU Leuven, and their co-workers have taken this principle a stage further and questioned if the intrinsic chirality of a building block (the “Sergeant”) can be overruled by using a chiral solvent (the “Corporal”).

They found that achiral porphyrin 1 could be forced to form chiral monolayers using (S)-and (R)-2-octanol as a solvent.  More impressively, they also found that the chirality of the assembly of chiral porphyrins (S)-2 and (R)-2 could be directed using these solvents.  The combination of (R)-2 and  (S)-2-octanol gave an enantiopure surface assembly, whereas using (R)-2-octanol resulted in a mixture of 2 different domains of opposite chirality.  Molecular dynamics simulations indicated that this could be due to hydrogen bonding between the solvent molecules and the amide groups of the porphyrins.  If more than one chiral centre was present (3 and 4), the chirality of the molecule was able to dominate the solvent effect.

This is a fascinating report of how a simple, weak interaction with solvent can overcome the inherent chirality of a stereogenic centre.  This work could lead to the preparation of bistable systems in which the chirality could be switched with a simple change of solvent.

Download this HOT ChemComm article today!

‘Sergeants-and-Corporals’ principle in chiral induction at an interface
Iris Destoop, Hong Xu, Cristina Oliveras-González, Elke Ghijsens, David B. Amabilino and Steven De Feyter
Chem. Commun., 2013, Advance Article
DOI: 10.1039/C3CC42584C

Cally Haynes is a guest web-writer for ChemComm.  She is currently a post doctoral researcher  at the University of Southampton, and her research interests include the supramolecular chemistry of anions.  When not in the laboratory, she likes travelling and watching football.

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ChemComm Emerging Investigators Issue 2013

A collection dedicated to internationally recognised, up-and-coming scientists from around the world.

Front coverWe are delighted to announce the publication of the 2013 ChemComm Emerging Investigators issue.

This is the third edition of this themed collection and we have been overwhelmed by the community’s positive response. I encourage you to take a look at the exceptional communications and feature reviews in this issue, as well as our previous issues in 2011 and 2012.

The issue contains over 90 Communications as well as a selection of Feature review articles, take a look at the whole collection today.

We invite you to submit your next communication article to ChemComm.

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Take 1.. minute for chemistry in health

Join this exciting video competition on the theme ‘How does chemistry keep us healthy?’ and win fantastic prizes!

Do you know how chemical scientists can tackle global challenges in Human Health?  If so, the RSC is running a one minute video competition this summer for young researchers such as PhD and Post-doc students; get involved and innovate the way scientists share their research.  Your video should communicate your own personal research or an area of research that interests you, highlighting its significance and impact to Human Health.

Five videos will be shortlisted by our judging panel and the winner will be selected during the ‘How does chemistry keep us healthy?’ themed National Chemistry Week taking place 16-23 November.

A £500 prize and a fantastic opportunity to shadow the award winning video Journalist, Brady Harran, is up for grabs for the winner.

The judging panel will include the makers of The Periodic Tale of Videos, Martyn Poliakoff and Brady Harran, and RSC Division representatives.

Check out our webpage for further details of the competition and an example video.

Closing date for entries is 01 July 2013.  Please submit your entries to rsc.li/take-1-video-competition.

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Releasing reactive oxygen

Scientists in Canada have made nanoparticles that release singlet oxygen when a laser beam is shone on them. The nanoparticles could improve the effectiveness of photodynamic therapy. 

Under the right conditions, oxygen, light and photosensitiser molecules combine to generate a short-lived poisonous oxygen species called singlet oxygen. This is the basis of photodynamic therapy, a treatment for some cancers. Normally, photodynamic therapy requires oxygen to be present in the target cells; however, tumours often contain much lower oxygen levels than healthy tissues.

Release of singlet oxygen from nanoparticles

Now, Neil Branda and colleagues at Simon Fraser University have developed a system that does not rely on oxygen being present. The team anchored anthracene endoperoxide ligands onto…

Continue reading the full article in Chemistry World »

Read the original journal article in ChemComm:
Photothermal release of singlet oxygen from gold nanoparticles
Amir Mahmoud Asadirad, Zach Erno and Neil R. Branda  
Chem. Commun., 2013, 49, 5639-5641
DOI: 10.1039/C3CC42217H

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Superpowers ahoy! Electric field causes DNA mutations

What can cause a mutation in DNA?  Well, if you were to ask the Incredible Hulk (nicely), he would probably say– well not a lot, he’s more of a doer, but Bruce Banner might tell you gamma rays.  But that is so 20th century.

In a Communication recently published in ChemComm, José Pedro Pedro Cerón-Carrasco (Université de Nantes) and Denis Jacquemin (Institut Universitaire de France) have shown that DNA can mutate permanently if an appropriate external electric field is applied.

Application of the right level of electric field can lead to proton transfer, which can cause the formation of tautomers, i.e. isomers of the DNA bases.  By interfering with the bases and their interaction, a mismatch or mutation can be induced.

Turn the power up a little more and soon I will become Science Girl!: The DNA tautomers form under the influence of an external electric field. Circles indicate the protons that have been shifted compared to the canonical structure: H1 in blue and H2 in red.

Cerón-Carrasco and Jacquemin used a computational model to assess the effects of both positive and negative external electric fields on a DNA model to achieve an in vivo-like outcome.  When applying an increasing strength of negative electric fields, they saw the more acidic H1 proton shift to the other base; intense positive fields activated the H2 proton.

The authors conclude that intense electric fields might damage DNA in a partially controlled way.  This could have exciting applications for biochemistry or medicine– for example, selectively mutating a disease-causing cell.  Or maybe, bestowing me with superpowers…

Interested in more?  Read this HOT ChemComm article in full!

Electric field induced DNA damage: an open door for selective mutations
José Pedro Pedro Cerón-Carrasco and Denis Jacquemin
Chem. Commun., 2013, Accepted Manuscript
DOI: 10.1039/C3CC42593B

Sarah Brown is a guest web-writer for Chemical Communications.  Sarah hung up her lab coat after finishing her PhD and post-doctorate in nanotechnology for diagnostics and therapeutics to become an assistant editor at the BMJ Publishing Group.  When not trying to explain science through ridiculous analogies, you can often find her crocheting, baking and climbing, but not all at once.


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Simple synthesis of heavy oxygen-labelled alcohols

Rozen and co-workers report a novel and extremely simple method for synthesising 18O-labelled alcohols using commercial boronic acids and a reagent prepared from elemental fluorine.

Alcohols labelled with 18O are very valuable as biological probes for a variety of studies which are often limited by the availability of labelled precursors for use in the synthesis of the compounds of interest.

Scientists in Israel prepared an 18O-labelled acetonitrile complex of hypofluorous acid by simply bubbling dilute F2 through acetonitrile and 18O-labelled water. They performed a series of reactions of this complex with a variety of aliphatic and aromatic boronic acids at room temperature to produce a series of 18O-labelled alcohols within just a few minutes and in excellent yields – generally upwards of 90 per cent.

Read this ‘HOT’ ChemComm Communication for free:

The first general route for efficient synthesis of 18O labelled alcohols using the HOF⋅CH3CN complex
Shlomo Rozen, Julia Luria and Inna Vints
Chem. Commun., 2013, Accepted Manuscript
DOI: 10.1039/C3CC42337A

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It’s getting hot in here…

Stimuli-responsive nanoparticles are the focus of much current research, and what could be better than a nanoparticle that responds to one stimulus?  A nanoparticle which responds to two or three.

Xianmao Lu and his team have coupled plasmonic silver nanoparticles to magnetic iron oxide nanoparticles and wrapped both in a thermoresponsive polymer – poly(n-isopropylacrylamide).

When illuminated by sunlight the silver nanoparticles absorb the light and convert it to heat.  The increase in temperature causes the polymer wrapping to collapse and reduces steric repulsion between the nanoparticle dimers leading to clustering.

Sunlight induced clustering of Magnetic-Plasmonic Heterodimers.

This clustering enhances the magnetic separation of the very small dimers from the solution (the nanoparticles are less than 9 nm each).  When you’ve caught the nanoparticles and are done with them, you can turn the lights off and they will re-disperse.

Don’t worry if you live in a cloudy part of the world, you can use a solar simulator to induce the clustering.  It would probably be easier to turn off than the sun, too.

To read the details, check out this HOT Chem Comm article in full:
Thermoresponsive Nanoparticles + Plasmonic Nanoparticles = Photoresponsive Heterodimers: Facile Synthesis and Sunlight-Induced Reversible Clustering
Hui Han, Jim Yang Lee and Xianmao Lu
Chem. Commun., 2013, 49, Accepted Manuscript
DOI: 10.1039/C3CC42273A

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Super Glue for cells

Red blood cells

Scientists in Canada have made a super-strong cell membrane adhesive and used it to stick red blood cells together. The polymer, based on the phospholipid head group phosphatidyl choline, could be used to secure cells in particular positions for tissue engineering and wound closure.

Don Brooks, from the Centre for Blood Research at the University of British Columbia, who led the study, says inspiration for the work came after trying to understand the chemistry of cell membranes. ‘Phosphatidyl choline [PC] is found in every cell membrane, except for some primitive bacteria, so we wondered what would happen if we were to turn the molecule around to choline phosphate [CP]? Would you get an adhesive effect because the positive and negative charges are now inverted?’ This proved to be the case, and the team demonstrated that branched polyglycerols containing CP bound to a variety of cell membranes

Read the full article in Chemistry World

Read the original journal article in ChemComm:
ATRP synthesis of poly(2-(methacryloyloxy)ethyl choline phosphate): a multivalent universal biomembrane adhesive
Xifei Yu, Xiaoqiang Yang, Sonja Horte, Jayachandran N. Kizhakkedathu and Donald E. Brooks 
Chem. Commun., 2013, Advance Article
DOI: 10.1039/C3CC41895B, Communication

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