Speakers confirmed for ISACS 12: Challenges in Chemical Renewable Energy

Challenges in Chemical Renewable Energy (ISACS12)
3 – 6 September 2013, Cambridge, UK

Confirmed invited speakers at  include:

 Photovoltaics

  • Professor Sir Richard Friend
    University of Cambridge, UK
  • Professor Tobin J. Marks
    Northwestern University, USA

Solar Fuels

  • Professor Daniel G. Nocera
    MIT (Massachusetts Institute of Technology), USA
  • Professor Harry B. Gray
    Caltech (California Institute of Technology), USA
  • Professor Dr Holger Dau
    Freie Universität Berlin, Germany
  • Professor Emily A. Carter
    Princeton University, USA

New battery materials

  • Professor Jean-Marie Tarascon
    University of Picardie Jules Verne, France
  • Professor Yang Shao-Horn
    MIT (Massachusetts Institute of Technology), USA
  • Professor Peter G. Bruce
    University of St Andrews, UK

Fuel cells

  • Professor Sossina M. Haile
    Caltech (California Institute of Technology), USA
  • Professor Fraser A. Armstrong
    University of Oxford, UK
  • Professor Ib Chorkendorff
    Technical University of Denmark

Molecular catalysis including bioinspired

  • Professor Shunichi Fukuzumi
    Osaka University, Japan
  • Professor Licheng Sun
    KTH Royal Institute of Technology, Sweden
  • Professor Matthias Beller
    Leibniz-Institut für Katalyse, Germany

ISACS 12 is now open for oral abstract submissions – submit your abstract for this exciting conference.

For more information visit the ISACS 12 website.Oral abstract deadline 3 May 2013
Poster abstract deadline 21 June 2013
Early bird registration deadline 12 July 2013

Important Deadlines:

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New coating for anticancer compounds improves generation of cancer-killing singlet oxygen

Phthalocyanines (Pcs) have excellent electronic and optical properties, which make them promising as a photosensitisers (PSs) for photodynamic therapy (PDT). Since Pcs strongly and selectively absorb light in the range of 600-800nm, they allow high penetration depth of light in normal tissue while minimising the risk and complications such as burning. But Pcs are highly hydrophobic and tend to form aggregates in aqueous media, which reduces their therapeutic activity.

Various types of nanocarriers, such as micelles, liposomes and nanoparticles, have been used to overcome this problem, and to prepare a stable dispersion of Pc in aqueous solution. However, most of them still suffer from shortcomings such as poor loading of Pc (small weight % of Pc in nanocarriers), risk of payload leaking before reaching target cells, and laborious, time-consuming fabrication and encapsulation processes.

Scientists in the Republic of Korea have made ZnPc nanospheres in one pot without using any templates or emulsifiers. They can be post-synthetically modified to improve their dispersibility in aqueous solution without altering their morphology or properties. They show higher singlet oxygen generation efficiency and in vitro phototoxicity than monomeric Pc molecules, suggesting that they are potentially useful as a photosensitiser for photodynamic therapy.

Targeting ligands could be introduced to deliver the nanospheres to specific target sites, anticipate the researchers. And if therapeutic agents were encapsulated, they could perform dual chemo- and photodynamic therapy.

Read this ‘HOT’ Chemical Science article:

Self-assembled, covalently linked, hollow phthalocyanine nanospheres
Raghunandan Hota, Kangkyun Baek, Gyeongwon Yun, Youngkook Kim, Hyuntae Jung, Kyeng Min Park, Eunjin Yoon, Taiha Joo, Juseok Kang, Chan Gyung Park, Su Mi Bae, Woong Shick Ahn and Kimoon Kim
Chem. Sci., 2012, DOI: 10.1039/C2SC21254D

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Super imaging of living cells

A new method of introducing single-molecule-quality fluorophores into live bacterial cells for superresolution imaging studies has been developed by researchers in the US.

Superresolution imaging can image structures with a spatial resolution 5 to 10 times smaller than the diffraction limit of about 200nm for visible wavelengths. In contrast to previous ideas, the team allows a permeable dye molecule (the substrate) to enter the cell in a fluorescently deactivated state.

Subsequent photoactivation by reaction with the enzyme nitroreductase produces fluorescent products whose concentration is controlled by the level of substrate uptake. Importantly, fluorophores can enter living cells fairly easily because they are neutral, and they emit at long wavelengths to avoid autofluorescence.

Read this ‘HOT’ Chemical Science article today:

Enzymatic Activation of Nitro-Aryl Fluorogens in Live Bacterial Cells for Enzymatic Turnover-Activated Localization Microscopy
Marissa K. Lee, Jarrod Williams, Robert Twieg, Jianghong Rao and W.E. Moerner
Chem. Sci., 2012, DOI: 10.1039/C2SC21074F

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Protein sorting within cells

Iron oxide nanoparticles coated with glutathione (purple), which is anchored by dopamine (yellow) and binds to the protein

Iron oxide nanoparticles coated with glutathione (purple), which is anchored by dopamine (yellow) and binds to the protein

US scientists have used magnetic nanoparticles with specific ligands to latch on to and visualise specific proteins in living cells. The approach could be used to identify new, selective ligands that bind proteins, which may help uncover drug–target interactions inside cells, say the researchers. Also, using magnetic nanoparticles means that the distribution, orientation and aggregation of cellular proteins could be controlled, leading to new ways to control the fate of cells.

A deeper understanding of protein function inside cells is essential as scientists try to find new ways to diagnose and treat disease. The first challenge is to locate the proteins involved and find out what they are doing, which is not an easy feat, considering the abundance of different proteins in our cells.

Read the full article in Chemistry World

Link to journal article
Magnetic nanoparticles for direct protein sorting inside live cells
Yue Pan ,  Marcus J. C. Long ,  Hsin-Chieh Lin ,  Lizbeth Hedstrom and Bing Xu
Chem. Sci., 2012, Advance Article, DOI: 10.1039/C2SC20519J

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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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