Chemical Science welcomes a new Associate Editor for Inorganic Materials

I am delighted to announce that Professor Jihong Yu (Jilin University, China) has joined the Chemical Science Editorial Board as the Associate Editor for Inorganic Materials.

Professor Yu’s research focuses on the designed synthesis of zeolitic porous functional materials. She obtained the National Outstanding Youth Fund of China in 2001, and was awarded National Prize for Natural Science in 2006, the 6th Chinese Youth Woman Scientist Award in 2009, and the Bau Family Award in 2010 for World Chinese Inorganic Chemists. She is now the Chief Scientist of the National Basic Research Project of China. 

Professor Yu’s Editorial Office will open for submissions imminently.

To submit your exceptional research to Professor Yu or any of our other outstanding Associate Editors, please use our online submission site.

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New way to capture sulfur dioxide

Scientists in Germany and Canada have developed a new way to capture sulfur dioxide gas. It could minimise the environmental impact of the gas, which causes acid rain.

The team made a series of frustrated Lewis pairs (FLPs) consisting of a bulky phosphane Lewis base component and a boron Lewis acid component. The FLPs rapidly and efficiently trap sulfur dioxide by adding the phosphane component to sulfur and the boron to oxygen.

Link to journal article
Reactions of Phosphorus/Boron Frustrated Lewis Pairs with SO2
M Sajid et al
Chem. Sci., 2012, DOI: 10.1039/c2sc21161k

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Protein surface study to design new stealth compounds

The surface chemistry of proteins makes them stable in complex biological environments. Scientists in the US have investigated why to enable peptide-based materials that resist non-specific interactions (stealth compounds) to be designed.

The cytoplasm is a crowded environment containing lots of different molecules but proteins resist non-specific interactions with these molecules. Understanding and mimicking nature’s resistance to non-specific interactions is key to addressing emerging challenges in chemistry, especially in practical applications where complex environments can degrade materials and surface coatings.

Here, the team has used structural bioinformatics to study proteins and molecular chaperones, which guide proteins from a misfolded or unfolded conformation back into a native conformation. They found that nature uses sequence design to modulate non-specific interactions so that the proteins function properly. Specifically, lysine and glutamic acid are the most abundant amino acids on the surface of proteins.

Link to journal article
Decoding nonspecific interactions from nature
A D White et al
Chem. Sci., DOI: 10.1039/c2sc21135a

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New source of MRSA antibiotic

Scientists in the UK have demonstrated that bottromycin (an antibiotic that works against MRSA) is biosynthesised from a larger precursor ribosomal peptide. This was proposed following a genome mining analysis of Streptomyces scabies and confirmed by a series of gene deletion experiments. The work also identifies S. scabies as a previously unknown producer of bottromycin. An almost identical gene cluster was also identified in S. bottropensis, an established bottromycin producer. Bottromycin is the first ribosomal peptide natural product that derives from the N-terminus of a larger prepeptide and the first terrestrial peptide to be directly ethylated at beta-positions.

Bottromycin is active in vitro but unstable in vivo so if scientists can engineer its biosynthesis to make unnatural analogues they might be able to make good new antibiotics. By identifying this pathway the team should facilitate the generation of a library of bottromycin-like antibiotics.

Link to journal article
Identification and characterisation of the gene cluster for the anti-MRSA antibiotic bottromycin: Expanding the biosynthetic diversity of ribosomal peptides
W J K Crone, F J Leeper and A W Truman
Chem. Sci., 2012, DOI: 10.1039/c2sc21190d

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Physical organic chemistry: An article collection

A free collection of high impact articles on physical organic chemistry from the RSC’s ChemComm, Chemical Science and Organic & Biomolecular Chemistry (OBC).

Model of a polycyclic aromatic hydrocarbonPhysical organic chemistry, the study of the underlying principles and rationale of organic reactions which looks at the interrelationships between the structure and reactivity of organic molecules, now encompasses a wider range of contexts than ever before

Making use of tools such as chemical kinetics, quantum chemistry, thermochemistry, chemical equilibrium and computational chemistry, to name but a few, researchers are investigating topics such as:

  • Supramolecular interactions, aggregation and reactivity
  • The computation of transition states and mechanisms
  • Molecular recognition, reactions and catalysis in biology
  • Materials where molecular structure controls function
  • Structure activity correlations
  • Mechanisms in synthesis and catalysis

To highlight some of the cutting edge research that ChemComm, Chemical Science and Organic & Biomolecular Chemistry publish we have collected a selection of articles for you to enjoy. These will be free to access until 25th September!

Click here for the full list of free articles

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Top ten most accessed articles in July

This month sees the following articles in Chemical Science that are in the top ten most accessed:-

Copper-catalyzed decarboxylative C-N coupling for N-arylation
Yun Zhang, Sejal Patel and Nello Mainolfi
Chem. Sci.,
2012, Advance Article, DOI: 10.1039/C2SC20606D, Edge Article

Copper-catalyzed decarboxylative alkenylation of sp3 C-H bonds with cinnamic acids via a radical process
Zili Cui, Xiaojie Shang, Xiang-Feng Shao and Zhong-Quan Liu
Chem. Sci.,
2012, Advance Article, DOI: 10.1039/C2SC20712E, Edge Article

Chiral ionic Brønsted acid-achiral Brønsted base synergistic catalysis for asymmetric sulfa-Michael addition to nitroolefins
Daisuke Uraguchi, Natsuko Kinoshita, Daisuke Nakashima and Takashi Ooi
Chem. Sci.,
2012, Advance Article, DOI: 10.1039/C2SC20698F, Edge Article

A chemical synthesis of 11-methoxy mitragynine pseudoindoxyl featuring the interrupted Ugi reaction
Jimin Kim, John S. Schneekloth and Erik J. Sorensen
Chem. Sci.,
2012,3, 2849-2852, DOI: 10.1039/C2SC20669B, Edge Article

Methane: a new frontier in organometallic chemistry
Vincent N. Cavaliere and Daniel J. Mindiola
Chem. Sci., 2012, Advance Article, DOI: 10.1039/C2SC20530K, Minireview

A fluorescent probe for rapid detection of hydrogen sulfide in blood plasma and brain tissues in mice
Yong Qian, Ling Zhang, Shuting Ding, Xin Deng, Chuan He, Xi Emily Zheng, Hai-Liang Zhu and Jing Zhao
Chem. Sci., 2012, Advance Article, DOI: 10.1039/C2SC20537H, Edge Article

Supramolecular mechanics in a metal-organic framework
Joseph M. Ogborn, Ines E. Collings, Stephen A. Moggach, Amber L. Thompson and Andrew L. Goodwin
Chem. Sci., 2012, Advance Article, DOI: 10.1039/C2SC20596C, Edge Article

Gold meets enamine catalysis in the enantioselective a-allylic alkylation of aldehydes with alcohols
Michel Chiarucci, Marzia di Lillo, Alessandro Romaniello, Pier Giorgio Cozzi, Gianpiero Cera and Marco Bandini
Chem. Sci., 2012,3, 2859-2863, DOI: 10.1039/C2SC20478A, Edge Article

Gram-scale synthesis and crystal structures of [8]- and [10]CPP, and the solid-state structure of C60@[10]CPP
Jianlong Xia, Jeffrey W. Bacon and Ramesh Jasti
Chem. Sci.,
2012, Advance Article, DOI: 10.1039/C2SC20719B, Edge Article

Catalytic enantioselective carbon-carbon bond formation using cycloisomerization reactions
Iain D. G. Watson and F. Dean Toste
Chem. Sci.,
2012, Advance Article, DOI: 10.1039/C2SC20542D, Minireview

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Chemical Science? Then why not submit to us today or alternatively contact us with your suggestions.

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Flipping the switch for discotic liquid crystals

Boronic esters have been used by US scientists to transform the triphenylene core in discotic liquid crystals (DLCs) from electron-rich to electron-deficient.

DLCs are used in electronic devices such as light emitting diodes. They need an electron-rich donor and an electron-poor acceptor. Current electron-poor acceptors have shortcomings including the fact that they can’t form columnar mesophases.

The team incorporated a boronic ester into the triphenylene core, which makes it an electron-poor acceptor and they were able to achieve broad mesophase temperature ranges.

Boronic Esters: A Simple Route to Discotic Liquid Crystals that Are Electron Deficient
Benjamin King and Luke Andrew Tatum
DOI: 10.1039/C2SC20128C

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Investigating protein interactions with anticancer drugs

New study provides insight into the possible mechanism of in vivo activation of platinum anticancer compounds

You can have too much of a good thing, in a manner of speaking. Cisplatin, a platinum-based anticancer drug, has been hugely successful in treating a range of cancers but severe side-effects require its administration to be dose-limited.  Analogues, such as carboplatin and nedaplatin have been developed to overcome these problems; carboplatin can be administered at 20 times the dosage of cisplatin.  These drugs, however, have their own problems and exhibit inherent and acquired toxicity.

Investigation into the uptake of platinum anticancer drugs has highlighted that the regulation of transport using carriers/ channel-mediated systems may be one of the key factors for drug resistance.  In particular, copper transporters and chaperones have been identified as participating in the uptake, transport and efflux of these drugs.

mechanism of in vivo activation of platinum anticancer compounds

The interactions of the N-terminus of hCTR1 with carboplatin

Hongzhe Sun and co-workers have advanced on previous work in which they employed NMR to  study metallodrug-biomolecule interactions. They identified that the methionine residues in the N-terminus of human CTR1 (hCTR1_N), a copper transporter, were essential to allow binding to cisplatin, potentially activating the drug.

Looking at carboplatin and nedaplatin as well as cisplatin’s clinically ineffective isomer, transplatin, the research team extended their studies to further understand the interaction between platinum compounds with hCTR1_N and compare their findings with cisplatin.

The NMR studies revealed that carboplatin and nedaplatin both bound to the methionine residues of the transporter, although when compared to cisplatin, less was activated. Interestingly, they are more stable than cisplatin, potentially due to shielding effects of their ligands. Transplatin was also found to bind to methionine residues at a much higher rate than its isomer.  This sophisticated investigation into the kinetics and speciation of platinum-based drugs gives greater understanding into drug-binding and insights into their distinct biological roles.

Read more about this research in Sun’s Chemical Science Edge article, free to access for a limited period.

Posted on behalf of Sarah Brown, Chemical Science web writer.

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Rotaxane molecular shuttles

Scientists in Canada have studied the synthetic scope of a new system of [2]rotaxane molecular shuttles based on a templating motif involving a benzimidazolium–crown ether recognition pair.

molecular shuttle

The template allows an array of molecular shuttles containing macrocyclic crown ethers of varying size and shape to be prepared.

The study also provides the beginnings of a property–structure relationship for molecular shuttling in this rigid, compact [2]rotaxane system. This could aid in the future design of [2]rotaxane molecular shuttles for incorporation into materials such as metal–organic frameworks.

Bis(benzimidazolium) axles and crown ether wheels: a versatile templating pair for the formation of [2]rotaxane molecular shuttles
Stephen J. Loeb, Kelong Zhu, V. Nicholas Vukotic and Nadim Noujeim
DOI: 10.1039/C2SC20986A

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Poster Prizes awarded at Electron Donor-Acceptor Interactions

Last week I attended the Gordon Research Conference (GRC) on Electron-Donor Acceptor Interactions in sunny Rhode Island. As per the rules of the GRC, I can’t divulge details of the science discussed but I am sure they won’t mind me saying that it was a fantastic conference – highly recommended!

One of the highlights of the meeting was the poster talks session. Here the three best poster presenters – as judged by the past and vice Chairs – were invited to give short oral presentations about their exciting research. I had the pleasure of awarding the Chemical Science and Energy & Environmental Science poster prizes to Geoffrey Hutchison (University of Pittsburgh) and Patrick Holder (MIT) respectively.

Gordon Research Conference
From left to right: Jim McCusker (Chair), Phillip Szuromi (Science magazine), Peter Dinolfo (Science poster prize winner), Geoffrey Hutchison (Chemical Science poster prize winner), Patrick Holder (EES poster prize winner), Bo Albinsson (Chair), Joanne Thomson (Chemical Science Deputy Editor)

Next week I’m back in the US at the Fall ACS meeting – let me know if you’d like to meet up. Or come and visit the RSC Booth 701, there’s a lot going on… 

 

 

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