Archive for the ‘News’ Category

Designer solvent hits hospital superbug

Scientists from Ireland, the Czech Republic and Spain have found an antimicrobial ionic liquid that targets MRSA (methicillin-resistant Staphylococcus aureus).  MRSA has made headlines in recent years as a superbug that is resistant to most standard antibiotics. The superbug is common in hospitals where patients have open wounds and weakened immune systems and at its peak, it was said to have caused 1652 deaths in the UK in 2006.

Research into finding potential antibiotic drugs against MRSA is ongoing, with many drugs currently being tested in clinical trials. Nicholas Gathergood, from Dublin City University, and colleagues, have prepared imidazolium-based ionic liquids from amino acid esters and dipeptidyl side chains as the building blocks. They tested the ionic liquids’ toxicity and found that the majority were non-toxic to microbes but two of them were highly toxic to Gram-positive bacteria, including MRSA. The two toxic compounds possessed a phenylalanine motif adjacent to the cation core. However, an analogue with a phenylalanine-phenylalanine sequence, an ionic liquid with increased lipophilicity, was less active (with no MRSA selectivity). A general trend in antimicrobial toxicity of ionic liquids is increased toxicity with increased lipophilicity. The compounds also passed ecotoxicity tests that show that they can be classed as biodegradable.

superbug MRSA
The hospital superbug MRSA is resistant to most standard antibiotics. Ionic liquids combine green chemistry and medicinal chemistry in a new way to fight it

Read the full story in Chemistry World

Link to journal article
Antimicrobial toxicity studies of ionic liquids leading to a ‘hit’ MRSA selective antibacterial imidazolium salt
Deborah Coleman ,  Marcel Špulák ,  M. Teresa Garcia and Nicholas Gathergood
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16090K

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Green Chemistry issue 3 now online

The latest issue of Green Chemistry is now online!

The front cover of this issue highlights work by Yong Huang (Peking University, China) and Hong Shen (Merck Research Laboratories, New Jersey, USA) and colleagues who report the synthesis of medicinally useful heterocycles such as pyridazinones and dihydropyrimidinones through a mild and highly efficient one-pot triple cascade procedure.  The cascade involves a Claisen-decarboxylation, an electrophilic reaction and subsequent heterocyclisation.  Indazoles and benzofurans could also be constructed through a double cascade reaction. 

One-pot synthesis of useful heterocycles in medicinal chemistry using a cascade strategy, Guiyong Wu, Weiyu Yin, Hong C. Shen and Yong Huang, Green Chem., 2012, 14, 580-585

The inside front cover features a Tutorial Review by Camilla Parmeggiani and Francesca Cardona from the University of Florence, Italy on transition metal based catalysts for the aerobic oxidation of alcohols.  The review covers advances in this area over the last 15 years, looking at transition metal catalysts in their various forms, i.e.homogeneous, heterogeneous or nanoparticles. 

Transition metal based catalysts in the aerobic oxidation of alcohols, Camilla Parmeggiani and Francesca Cardona, Green Chem., 2012, 14, 547-564

These articles have been made free to access for 6 weeks!

Stay up-to-date with the latest content in Green Chemistry by registering for our free table of contents alerts.

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Top ten most accessed articles in January

This month sees the following articles in Green Chemistry that are in the top ten most accessed:-

Continuous flow reactors: a perspective
Charlotte Wiles and Paul Watts
Green Chem., 2012, 14, 38-54, DOI: 10.1039/C1GC16022B

How do the fine chemical, pharmaceutical, and related industries approach green chemistry and sustainability?
William J. W. Watson
Green Chem., 2012, 14, 251-259, DOI: 10.1039/C1GC15904F

Energy-efficient extraction of fuel and chemical feedstocks from algae
Rodrigo E. Teixeira
Green Chem., 2012, 14, 419-427, DOI: 10.1039/C2GC16225C

Environmentally benign synthesis of heterocyclic compounds by combined microwave-assisted heterogeneous catalytic approaches
Arif Daştan, Aditya Kulkarni and Béla Török
Green Chem., 2012, 14, 17-37, DOI: 10.1039/C1GC15837F

Chitosan functionalized ionic liquid as a recyclable biopolymer-supported catalyst for cycloaddition of CO2
Jian Sun, Jinquan Wang, Weiguo Cheng, Jianxin Zhang, Xiaohua Li, Suojiang Zhang and Yuanbin She
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16335G

Poly(ethylene glycol)-functionalized imidazolium salts-palladium-catalyzed Suzuki reaction in water
Ning Liu, Chun Liu and Zilin Jin
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16486H

Highly efficient conversion of carbon dioxide catalyzed by polyethylene glycol-functionalized basic ionic liquids
Zhen-Zhen Yang ,  Ya-Nan Zhao ,  Liang-Nian He ,  Jian Gao and Zhong-Shu Yin
Green Chem., 2012, 14, 519-527, DOI: 10.1039/C2GC16039K

DABCO-Promoted three-component regioselective synthesis of functionalized chromen-5-ones and pyrano[3,2-c]chromen-5-ones via direct annulation of a-oxoketene-N,S-arylaminoacetals under solvent-free conditions
Maya Shankar Singh, Ganesh Chandra Nandi and Subhasis Samai
Green Chem., 2012, 14, 447-455, DOI: 10.1039/C1GC16129F

L-Proline catalysed multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction under solvent-free conditions
Atul Kumar, Maneesh Kumar Gupta and Mukesh Kumar
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC16297G

A sustainable process for the production of γ-valerolactone by hydrogenation of biomass-derived levulinic acid
Anna Maria Raspolli Galletti, Claudia Antonetti, Valentina De Luise and Marco Martinelli
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC15872H

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

Fancy submitting an article to Green Chemistry? Then why not submit to us today or alternatively email us your suggestions.

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Green Chemistry Chair receives two more scientific acolades

Professor Martyn Poliakoff from the University of Nottingham and Chair of the Green Chemistry Editorial Board, has been awarded the Royal Society of Chemistry’s Nyholm Prize for Education and has been elected as a foreign member of the Russian Academy of Sciences.

The Nyholm Prize for Education, in honour of Sir Ronald Hyholm, has been awarded to Professor Poliakoff for his work in bringing a whole new audience to chemistry through the Periodic Table of Videos.  Professor Poliakoff said:

“I was really happy to be awarded the Nyholm Prize which I regard as a prize for the whole of the Periodic Table of Videos team. It is particularly gratifying as Sir Ronald Nyholm, in whose honour this prize is named, was a hugely important figure in both chemical research and chemical education.”

Professor Poliakoff will present a talk entitled ‘From Test Tube to YouTube’ at the RSC Education Division Nyholm Symposium at the University of Nottingham on Wednesday the 8th February. 

Professor Poliakoff has also been elected as a foreign member of the Russian Academy of Sciences, an honour which is particularly special due to his own strong links with the country. 

Green Chemistry would like to extend our warmest congratulations to Professor Poliakoff.

 

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Green Chemistry Issue 2 now online!

The latest issue of Green Chemistry is now available online.

The front cover of this issue features work by Rodrigo Teixeira from the University of Alabama in Huntsville, USA who reports the energy efficient extraction of fuel and chemical feedstocks from algae.  The deconstruction of algae cell walls and release of the cells contents was achieved by dissolution and hydrolysis of wet algae biomass in ionic liquids.  This process does not require acids, bases or any other catalysts, and can be completed in less than 50 mins (regardless of the algae species) at 100-140 °C and atmospheric pressure. 

Energy-efficient extraction of fuel and chemical feedstocks from algae, Rodrigo E. Teixeira, Green Chem., 2012, 14, 419-427

The inside front cover highlights work by Richard Daniellou, Daniel Plusquellec and colleagues from the National School of Chemistry of Rennes and the European University of Brittany, France, who report aqueous solutions of facial amphiphilic carbohydrates as a sustainable media for organocatalyzed direct aldol reactions.  Their system was applied to the direct aldol reaction of m-nitrobenzaldehyde with various cyclohexanones, and proceeded with high yields, shortened reaction times and improved diastereoselectivities. 

Aqueous solutions of facial amphiphilic carbohydrates as sustainable media for organocatalyzed direct aldol reactions, Ana Bellomo, Richard Daniellou and Daniel Plusquellec, Green Chem., 2012, 14, 281-284

Read these articles for free until the 14th March 2012!

Stay up-to-date with the latest content in Green Chemistry by registering for our free table of contents alerts!

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Top ten most accessed articles in December

This month sees the following articles in Green Chemistry that are in the top ten most accessed:-

Conversion of carbohydrates and lignocellulosic biomass into 5-hydroxymethylfurfural using AlCl3·6H2O catalyst in a biphasic solvent system
Yu Yang, Chang-wei Hu and Mahdi M. Abu-Omar
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC15972K

l-Proline catalysed multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction under solvent-free conditions
Atul Kumar, Maneesh Kumar Gupta and Mukesh Kumar
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC16297G

Recent advances in ionic liquid catalysis
Qinghua Zhang, Shiguo Zhang and Youquan Deng
Green Chem., 2011, Advance Article, DOI: 10.1039/C1GC15334J

Rh(i) complexes supported on a biopolymer as recyclable and selective hydroformylation catalysts
Banothile C. E. Makhubela, Anwar Jardine and Gregory S. Smith
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC15979H

Ionic liquids from renewable biomaterials: synthesis, characterization and application in the pretreatment of biomass
Qiu-Ping Liu, Xue-Dan Hou, Ning Li and Min-Hua Zong
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16128A

Ionic liquid mediated one-pot synthesis of 6-aminouracils
Sunil S. Chavan and Mariam S. Degani
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC15940B

Green synthesis of metal nanoparticles using plants
Siavash Iravani
Green Chem., 2011, 13, 2638-2650, DOI: 10.1039/C1GC15386B

Liquid hydrocarbon fuels from cellulosic feedstocks via thermal deoxygenation of levulinic acid and formic acid salt mixtures
Paige A. Case, Adriaan R. P. van Heiningen and M. Clayton Wheeler
Green Chem., 2012, 14, 85-89, DOI: 10.1039/C1GC15914C

Conversion of fructose and inulin to 5-hydroxymethylfurfural in sustainable betaine hydrochloride-based media
Karine De Oliveira Vigier, Adlene Benguerba, Joël Barrault and François Jérôme
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC16236E

Aqueous solutions of facial amphiphilic carbohydrates as sustainable media for organocatalyzed direct aldol reactions
Ana Bellomo, Richard Daniellou and Daniel Plusquellec
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC16326D

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

Fancy submitting an article to Green Chemistry? Then why not submit to us today or alternatively email us your suggestions.

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Systematic optimization of a biocatalytic two-liquid phase oxyfunctionalization process guided by ecological and economic assessment

Scientists from Germany have optimized and assessed the ecological performance of a whole-cell two-liquid phase biocatalytic epoxidation of styrene.

Bruno Bühler and colleagues from the Technical University of Dortmund and Saarland University, Germany, considered how the ecological aspects of this reaction could be improved.  Currently, the ecological performance is hampered by the organic carrier solvent employed (bis(2-ethylhexyl)phthalate) which is toxic to humans and is produced from non-renewable resources.  Instead ethyl oleate (a biodiesel constituent) was tested and shown to be an environmentally attractive and cost-competitive solvent.

The authors also replaced the carbon/energy source glucose with glycerol as the latter is a waste product from the biodiesel and soap industries and thus cheap and abundant.  However, the use of glycerol was found to reduce the overall ecological and economic performance of the process.  The work presented here by Bühler and co-workers illustrates the capability of these assessments to identify critical process parameters and to enable systematic development towards industrial implementation.

This article is free to access until the 24th February 2012!  Click on this link below to find out more…

Systematic optimization of a biocatalytic two-liquid phase oxyfunctionalization process guided by ecological and economic assessment, Daniel Kuhn, Mattijs K. Julsing, Elmar Heinzle and Bruno Bühler, Green Chem., 2012, DOI: 10.1039/C2GC15985F

You may find this article of interest too – also free to access until the 24th February 2012, so why not take a look…

Intensification and economic and ecological assessment of a biocatalytic oxyfunctionalization process, Daniel Kuhn, Muhammad Abdul Kholiq, Elmar Heinzle, Bruno Bühler and Andreas Schmid, Green Chem., 2010, 12, 815-827

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Tailor-made biopolymers from leather waste valorisation

Scientists from Spain report tailor-made collagen biopolymers from tanning waste with diverse shapes such as fibers, films and sponges. 

Mercedes Catalina (Advanced Chemistry Institute of Catalunya), Rafael Luque (University of Cordoba) and colleagues valorised tanning waste from leather processing to give biopolymers which could be easily modified using various methodologies with the aim of generating waste-derived renewable biopolymers.  For example, introducing cross-linking agents on the  matrix network of the biopolymer provided a material with improved properties.  The authors envisage these materials could have promising in fields such as cosmetics and medicines.

This article is free to access until the 18th February 2012! Click on the link below to find out more…

Tailor-made biopolymers from leather waste valorisation, Mercedes Catalina, Jaume Cot, Alina Mariana Balu, Juan Carlos Serrano-Ruiz and Rafael Luque, Green Chem., 2012, DOI: 10.1039/C2GC16330F

You may find this review article of interest too which is also free to access.  Why not take a look…

Waste materials – catalytic opportunities: an overview of the application of large scale waste materials as resources for catalytic applications, M. Balakrishnan, V. S. Batra, J. S. J. Hargreaves and I. D. Pulford, Green Chem., 2011, 13, 16-24

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Linseed and soybean oil-based polyurethanes prepared via the non-isocyanate route and catalytic carbon dioxide conversion

Soy- and linseed oil-based polyurethanes were synthesized by curing carbonated soybean and linseed oils with different diamines. 

Moritz Bähr and Rolf Mülhaupt from the Freiburg Materials Research Center (FMF) and Department of
Macromolecular Chemistry, Germany, have developed a non-isocyante route to soy- and linseed oil-based polyurethanes.  The route involved conversion of the epoxidised seed oils with carbon dioxide to form cyclic carbonates catalysed by tetra-butylammonium bromide and silica supported 4-pyrrolidinopyridium iodide.  The catalysts could be easily recovered without needing traditional solvent extraction.  The resulting carbonates were then cured with various amines to give the polyurethanes.

As well as avoiding the use of toxic chemicals, this route also led to some polkyurethanes with increased glass transition temperatures and improved stiffness.  To find out more, just click on the article link below.  This article is currently free to access until the 15th February 2012!

Linseed and soybean oil-based polyurethanes prepared viathe non-isocyanate route and catalytic carbon dioxide conversion, Moritz Bähr and Rolf Mülhaupt, Green Chem., 2012, DOI: 10.1039/C2GC16230J

You may also find these articles of interest – free to access until the 15th February 2012 too!  So why not take a look…

Biorenewable polyethylene terephthalate mimics derived from lignin and acetic acid, Laurent Mialon, Alexander G. Pemba and Stephen A. Miller, Green Chem., 2010, 12, 1704-1706

Vegetable oil-based polymeric materials: synthesis, properties, and applications, Ying Xia and Richard C. Larock, Green Chem., 2010, 12, 1893-1909

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Green Chemistry article in C&EN

A recently published Green Chemistry aricle by David Cole-Hamilton (University of St. Andrews, UK), Stefan Mecking (University of Konstanz, Germany) and colleagues has just been featured in the latest issue of Chemistry & Engineering News (C&EN). 

The paper reports the synthesis of the diester dimethyl 1,19-nonadecanedioate from the palladium catalysed methoxycarbonylation of various commerial oils, including olive and sunflower oils.  The resulting product can then be easily converted to the diol and diacid, and all three chemicals can serve as useful polymer precursors. 

This article is now free to access until the 15th February 2012!  Click the link below to find out more…

Polymer precursors from catalytic reactions of natural oils, Marc R. L. Furst, Ronan Le Goff, Dorothee Quinzler, Stefan Mecking, Catherine H. Botting and David J. Cole-Hamilton, Green Chem., 2012, DOI: 10.1039/C1GC16094J

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