Archive for the ‘Subject Areas’ Category

Synthesising gold- and silver-NHC complexes using a weak base

Scientists from the University of Zaragoza in Spain have developed a simple and efficient method of synthesising N-heterocyclic carbene (NHC) gold and silver complexes with the use of an extremely weak base1.

Gold-NHC complexes are commercially important precursors of active, luminescent species that catalyse many useful reactions, such as cycloisomerisation, rearrangement of allylic acetates, C-H activation, carbene transfer, polymerisation, among others.  In addition, they have potentially significant applications in the synthesis of new pharmaceuticals and natural products.

Conventional methods of gold-NHC synthesis– the generation of free NHC and the Ag-carbene transfer route– present several logistic and economic limitations, such as the need for an inert atmosphere and the use of additives.  These methods are not always efficient, and typically require complicated working conditions in order to produce even moderate yields.

M. Concepción Gimeno and her team’s novel and elegant one-pot synthetic route involves isolating imidazolium salts using [AuCl(tht)] (tht = tetrahydrothiophene) in the presence of a mild base, such as K2CO3, to produce gold-NHC complexes with very high yields (91-94%) over relatively short reaction times (1.5 hours).

c3cc42919a-s2

Similarly, Gimeno et al. found that, using the same mild base protocol, silver-NHC complexes could also be efficiently synthesised using AgNO3, with vast potential significance in transmetalation.

c3cc42919a-s3

In both routes, the reactions occur under ambient conditions, eliminating the need to work in an argon atmosphere, and using readily-available technical grade solvents.

Interestingly, a mere few days later, Gimeno et al.‘s groundbreaking work was followed closely and independently by a related Communication from Steven Nolan’s group at the University of St Andrews.  In addition to testing a similar methodology, Nolan’s team compared small- and larger-scale reactions, and characterised compounds by 1H and 13C{1H} NMR spectroscopies, as well as by elemental analysis2.

To find out more about these fascinating breakthroughs in organometallics, read these HOT ChemComm articles now for free!

1.  Simple and efficient synthesis of [MCI(NHC)] (M = Au, Ag) complexes
Renso Visbal, Antonio Laguna and M. Concepción Gimeno
Chem. Commun., 2013, 49
DOI: 10.1039/C3CC42919A, Communication

2.  Straightforward synthesis of [Au(NHC)X] (NHC = N-heterocyclic carbene, X = Cl, Br, I) complexes
Alba Collado, Adrián Gómez-Suárez, Anthony R. Martin, Alexandra M. Z. Slawin and Steven P. Nolan
Chem. Commun., 2013, 49
DOI: 10.1039/C3CC43076F, Communication

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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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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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Photocatalysis in a nanocup

Written by Geoff Nelson, web writer.

Nanocups of anatase TiO2 coated with Au nanoparticles are efficient photocatalysts, as reported in a recent ChemComm article by Chemical Science and Chem Soc Rev Advisory Board member Jinlong Gong and  his group at Tianjin University, China.

This new shape promises to increase reactive surface area by exposing the normally inaccessible surface of hollow spheres.  Compared to TiO2 hollow spheres, TiO2 nanocup particles increase the rate of the photocatalytic degradation of methylene blue in the visible light region by 46%.

This performance and the ease of nanocup synthesis are reasons to promote further research.  Thus, we may expect nanocups made from other metal oxides and inorganic materials to be incorporated into solar, photochemical, and catalytic applications in the future.

In addition, the ability of nanocups to confine small amounts of reactants may find utility in nanofluidic devices.

Gong et al.‘s work has recently been highlighted as part of a C&EN article on novel nanostructures.

Read this ChemComm article in full:

Mesoporous anatase TiO2 nanocups with plasmonic metal decoration for highly active visible-light photocatalysis

Jianwei Lu, Peng Zhang, Ang Li, Fengli Su, Tuo Wang, Yuan Liu and Jinlong Gong
Chem. Commun., 2013, Advance Article
DOI: 10.1039/C3CC42029A

Geoff Nelson is a guest web-writer for ChemComm.  He currently works as a post-doctoral research associate in Dr David Payne’s research group in the Department of Materials at Imperial College, London.  Geoff’s current research concerns the synthesis and characterization of post-transition metal oxides for use in the energy sector.  His other research interests include carbon-based materials, biophysical chemistry, and surface science.

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ChemComm Emerging Investigator Lectureship 2013: Winners Announced

louise

Louise Berben

On behalf of the ChemComm Editorial Board we are delighted to announce the winners of the ChemComm Emerging Investigator Lectureship 2013.

Marina Kuimova

Marina Kuimova

This year we received a high number of excellent nominations and therefore the Editorial Board have decided to award two Emerging Investigator Lectureships in 2013. The winners are Professor Louise A. Berben (University of California Davis, USA) and Dr Marina Kuimova (Imperial College London).

This annual lectureship recognises an emerging scientist in the early stages of their independent academic career.

The Editorial Board commended Louise’s contributions to the field of synthetic and physical inorganic chemistry, and Marina was awarded the lectureship for her excellent work within biophysical chemistry. Further details of the two Lectureships, including lecture locations, will be announced soon.

To find out more about the winners’ research, read some of their latest articles in ChemComm:

Redox active aluminium(III) complexes convert CO2 into MgCO3 or CaCO3 in a synthetic cycle using Mg or Ca metal
Thomas W. Myers and Louise A. Berben
Chem. Commun., 2013, DOI: 10.1039/C2CC37208H

Simple routes to bulky silyl-substituted acetylide ligands and examples of V(III), Fe(II), and Mn(II) complexes
Gereon M. Yee, Kristin Kowolik, Shuhei Manabe, James C. Fettinger and Louise A. Berben
Chem. Commun., 2011,47, 11680-11682, DOI: 10.1039/C1CC14758G

Reactive oxygen species in photochemistry of the red fluorescent protein “Killer Red”
Russell B. Vegh, Kyril M. Solntsev, Marina K. Kuimova, Soohee Cho, Yue Liang, Bernard L. W. Loo, Laren M. Tolbert and Andreas S. Bommarius
Chem. Commun., 2011,47, 4887-4889, DOI: 10.1039/C0CC05713D

Also of interest: You can now browse the 2013 Emerging Investigators Issue – which features research from outstanding up-and-coming scientists

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Cram Lehn Pedersen Prize winner Tomoki Ogoshi: US lectures 2013

Our 2013 Cram Lehn Pedersen Prize winner, Professor Tomoki Ogoshi (Kanazawa University, Japan), is set to visit the US this year to deliver his award lectures.

Tomoki Ogoshi will first present his lecture, entitled “Pillararenes: Easy-to-make and versatile receptors for supramolecular chemistry,” at the 8th International Symposium on Macrocyclic and Supramolecular Chemistry (8-ISMSC) in Crystal City, Virginia, USA from 7-11 July 2013.

Later in the year, Tomoki Ogoshi will speak at the University of Texas at Austin (20 Sept) where he will be hosted by ChemComm Associate Editor Professor Jonathan Sessler.  He will then travel to San Diego, CA, to present his talk at the Scripps Research Institute (23 Sept), hosted by Professor Julius Rebek, Jr.

Register online for the 8-ISMSC between now and 1 July to catch Professor Ogoshi’s first award lecture this summer– reduced fees for students and post-docs are available!

2013 ISMSC-8

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ChemComm-RSC Prizes and Awards Symposium: Supramolecular Chemistry

We invite you to join us for the ChemComm-RSC Prizes and Awards Symposium which will be taking place on 24 May 2013 in Dublin, Ireland.

This free one-day event will comprise of stimulating lectures reflecting the academic and industrial breadth of supramolecular chemistry, delivered by RSC Prize and Award winners and leaders in the field.

Confirmed Speakers:

  • 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

We hope you and your colleagues will be able to attend the ChemComm-RSC Prizes and Awards Symposium. For further information about this event and to register, please visit the dedicated webpage.

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