The 2nd International Symposium on Green Chemistry Renewable Carbon and Eco-Efficient Processes (ISGC2)

From left to right: Sarah Ruthven, Professor Tao Zhang, Cinthia Mena Duran and Professor Walter Leitner

The 2nd International Symposium on Green Chemistry Renewable Carbon and Eco-Efficient Processes (ISGC2) was held from May 21–24th in La Rochelle, France. The conference aimed to cover the crucial problems arising from the conversion of renewable carbon and also the recent advances in the search of innovative processes for the conversion of biomass and wastes with high eco-efficiency.

The speakers included Green Chemistry Editorial Board members Professors Walter Leitner, Chao-Jun Li, Paul Anastas and Shu Kobayashi, and Advisory Board members Professors James Clark, Avelino Corma and Philip Jessop.

Professor Walter Leitner, Chair of the Green Chemistry Editorial Board, and Sarah Ruthven, Editor of Green Chemistry, presented the Green Chemistry sponsored poster prizes. The winners were Cinthia Mena Duran for her poster ‘Applications of Starbons’ and Guangyi Li for the poster ‘Synthesis of renewable diesel with 2-methylfuran and hydroxyacetone’. Congratulations to Cinthia and Guangyi on receiving these prizes.

Green Chemistry is pleased to be publishing a themed issue containing selected papers from the ISGC2 conference, which will be appearing later this year.

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The 10th Congress on Catalysis Applied to Fine Chemicals

The 10th Congress on Catalysis Applied to Fine Chemicals will be held in Turku, Finland on June 16–19th. The congress is devoted to the application of any type of catalyst (homogeneous, heterogeneous, enzymatic) to the synthesis of fine chemicals, with special emphasis on the selectivity issues. The aim is to bring together researchers from both academia and industry, working in the synthesis of fine chemicals with various catalysts, to share their expertise in the field as a way to open new collaborations that help to solve the forthcoming problems in the chemical industry, and to implement more sustainable synthetic methods based on catalytic processes. Click here to register today!

Plenary Lectures include:

Kurt Faber, University of Graz
 • Adding Value: Biocatalytic Carboxylation of Aromatics and Asymmetric Hydration of Alkenes

David Milstein, The Weizmann Institute of Science
 • Design of Sustainable Catalytic Reactions Based on Cooperative Pincer Systems

Peter McBreen, Université Laval
 • Single-Diastereomer Studies of Enantioselective Reactions on Metal Surfaces

Aurel Wolf, Bayer Technology Services GmbH
 • CO2 as C1 Building Unit for Chemicals and Polymers

Angelo Vaccari, University of Bologna
 • Examples of Environmentally Friendly Applications of the  Heterogeneous Catalysis  in Fine Chemistry

Dr. Heikki Hassila, Pharmatory Oy, Oulu Finland
 • Enzymatic Tools for Preparation of Chiral APIs and Key Building Blocks

Deputy Editor Anna Simpson will be attending CAFC10, if you would like to meet her there, please email green-rsc@rsc.org

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Green Chemistry issue 6 is now available online

Issue 6 of Green Chemistry is now available to read online.

C3GC40388B cover imageThe front cover this month features work by Mihai Irimia-Vladu and co-workers from Linz, Austria. In their work, they report the use of the natural resin shellac in organic field-effect transistors. Biocompatible and sustainable electronic-grade materials such as shellac are integral for the development of electronics for biointegration and ‘use-and-throw’ applications.

Read the full article:
Natural resin shellac as a substrate and a dielectric layer for organic field-effect transistors
M. Irimia-Vladu, E.D. Głowacki, G. Schwabegger, L. Leonat, H.Z. Akpinar, H. Sitter, S. Bauer and N.S. Sariciftci  
Green Chem., 2013, 15, 1473-1476,  DOI: 10.1039/C3GC40388B

 

C3GC37141G cover imageThe inside front cover this month features work by Bert F. Sels and co-workers from Heverlee, Belgium. In their work, they look at how ordered porous inorganic–organic nanocomposites and nanohybrids enable the acquirement of tailor-made properties, resulting in highly performing catalysts for applications in fine chemistry and biomass conversion.

Read the full article:
Tailoring nanohybrids and nanocomposites for catalytic applications
F. de Clippel, M. Dusselier, S. Van de Vyver, L. Peng, P.A. Jacobs and B.F. Sels  
Green Chem., 2013, 15, 1398-1430, DOI: 10.1039/C3GC37141G

 

Both of these articles are free to access for 6 weeks!

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

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HOT papers in Green Chemistry

Here are the latest HOT papers published in Green Chemistry, as recommended by the referees:

Soy-castor oil based polyols prepared using a solvent-free and catalyst-free method and polyurethanes therefrom
Chaoqun Zhang, Ying Xia, Ruqi Chen, Seungmoo Huh, Patrick A. Johnston and Michael R. Kessler  
Green Chem., 2013,15, 1477-1484, DOI: 10.1039/C3GC40531A

graphical abstract for c3gc40531a

 

Carbon dioxide as a reversible amine-protecting agent in selective Michael additions and acylations
Annelies Peeters, Rob Ameloot and Dirk E. De Vos  
Green Chem., 2013,15, 1550-1557, DOI: 10.1039/C3GC40568K

graphical abstract for c3gc40568k

 

Development of GSK’s reagent guides – embedding sustainability into reagent selection
Joseph P. Adams, Catherine M. Alder, Ian Andrews, Ann M. Bullion, Matthew Campbell-Crawford, Michael G. Darcy, John D. Hayler, Richard K. Henderson, Catriona A. Oare, Israil Pendrak, Anikó M. Redman, Leanna E. Shuster, Helen F. Sneddon and Matthew D. Walker  
Green Chem., 2013,15, 1542-1549, DOI: 10.1039/C3GC40225H

graphical abstract for c3gc40225h

 

All the papers listed above are free to access for the next 4 weeks!

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17th Annual Green Chemistry & Engineering Conference – Sustainable Chemistry & Engineering in the 21st Century

The ACS Green Chemistry Institute®’s Green Chemistry & Engineering Conference (GC&E) will be held on the 18–20 June 2013 in North Bethesda, Maryland, just outside of Washington DC. This event is an opportunity for scientists, businesses, students and educators, and advocates to broaden their understanding of green chemistry and engineering while building valuable connections with leaders in this growing field.

GC&E features three days of programming including world-renowned speakers, three poster sessions and more than 30 technical sessions on subjects such as designing safer chemicals and products, green chemistry education, and new business through green chemistry innovations.

Conference Highlights

• Daily Keynotes Speakers:  There will be a daily keynote presentation from Dr. Milton Hearn, Associate-Director, Green Chemical Futures-Industry; Dr. Michael J. Pcolinski, Vice President of Innovation & Technology, BASF Corporation; and Dr. Jim Hutchison, Professor of Chemistry, University of Oregon.

GC&E Student Workshop: This pre-conference workshop will be Monday, 17 June 2013 and is free to students registered for the conference. Lead by ACS Green Chemistry Institute® Director, Dr. David Constable, and other experts, this workshop will be a fast pasted, interactive series of sessions covering each of the 12 Principles of Green Chemistry.

ACS Careers Workshop: On Wednesday, 19 June 2013, expert consultants from ACS Careers will conduct a 4-hour workshop to help attendees accelerate professional development. Learn more about planning and résumé preparation, maintaining an effective job search, reviewing employment trends, and enhancing professional skills.

Online Session: A special session “Global Supplies for Chemical Feedstocks in the 21st Century” will be held on Tuesday, 18 June 2013 at 7:00 p.m. EDT (–4 GMT) and streamed live online for free to viewers around the world.

The Green Expo: The expo features vendors from business, government, and academia. Explore some of the 21st Century’s latest technology, resources, and marketplace opportunities.

For more information and to register, please visit the website www.gcande.org.

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Top 10 most accessed articles in February

For Green Chemistry, the top 10 most accessed articles in February were as follows:

Deconstruction of lignocellulosic biomass with ionic liquids
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton  
Green Chem., 2013, 15, 550-583
DOI: 10.1039/C2GC36364J, Critical Review

Iron-catalyzed direct alkenylation of sp3(C–H) bonds via decarboxylation of cinnamic acids under ligand-free conditions
Hailong Yang, Hong Yan, Peng Sun, Yan Zhu, Linhua Lu, Defu Liu, Guangwei Rong and Jincheng Mao  
Green Chem., 2013, 15, 976-981
DOI: 10.1039/C3GC37131J, Paper

Glycerol carbonate as a versatile building block for tomorrow: synthesis, reactivity, properties and applications
Matthieu O. Sonnati, Sonia Amigoni, Elisabeth P. Taffin de Givenchy, Thierry Darmanin, Olivier Choulet and Frédéric Guittard  
Green Chem., 2013, 15, 283-306
DOI: 10.1039/C2GC36525A, Critical Review

Food waste biomass: a resource for high-value chemicals
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly Budarin and James H. Clark  
Green Chem., 2013, 15, 307-314
DOI: 10.1039/C2GC36978H, Perspective

Ohmic heating as a new efficient process for organic synthesis in water
Joana Pinto, Vera L. M. Silva, Ana M. G. Silva, Artur M. S. Silva, José C. S. Costa, Luís M. N. B. F. Santos, Roger Enes, José A. S. Cavaleiro, António A. M. O. S. Vicente and José A. C. Teixeira  
Green Chem., 2013, 15, 970-975
DOI: 10.1039/C3GC36881E, Paper

Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
David Martin Alonso, Stephanie G. Wettstein and James A. Dumesic  
Green Chem., 2013, 15, 584-595
DOI: 10.1039/C3GC37065H, Critical Review

Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions
Maya Shankar Singh, Anugula Nagaraju, Girijesh Kumar Verma, Gaurav Shukla, Rajiv Kumar Verma, Abhijeet Srivastava and Keshav Raghuvanshi  
Green Chem., 2013, 15, 954-962
DOI: 10.1039/C3GC37047J, Paper

Catalytic etherification of glycerol with short chain alkyl alcohols in the presence of Lewis acids
Fei Liu, Karine De Oliveira Vigier, Marc Pera-Titus, Yannick Pouilloux, Jean-Marc Clacens, Floryan Decampo and François Jérôme  
Green Chem., 2013, 15, 901-909
DOI: 10.1039/C3GC36944G, Paper

Selective oxidation of alcohols and aldehydes over supported metal nanoparticles
Sara E. Davis, Matthew S. Ide and Robert J. Davis  
Green Chem., 2013, 15, 17-45
DOI: 10.1039/C2GC36441G, Critical Review

Multicomponent reactions in unconventional solvents: state of the art
Yanlong Gu  
Green Chem., 2012, 14, 2091-2128
DOI: 10.1039/C2GC35635J, Critical Review
Take a look at the articles, and then let us know your thoughts and comments below.

Fancy submitting your own work to Green Chemistry? You can submit online today, or email us with your ideas and suggestions.

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Green Chemistry issue 5 now available online!

Issue 5 of Green Chemistry is now available to read online.

The front cover (left) this month features work by Etienne Grau and Stefan Mecking from Konstanz, Germany. In their work, caryophyllene and humulene, renewable sesquiterpenes from clove oil, were subject to metathesis polymerization to yield non-crosslinked linear polymers with unique microstructures and low glass transition temperatures.

Read the research: Polyterpenes by ring opening metathesis polymerization of caryophyllene and humulene, E. Grau and S. Mecking, Green Chem., 2013, 15, 1112–1115, DOI: c3gc40300a

The inside front cover (right) this month features work by Thomas-Xavier Métro, Frédéric Lamaty and co-workers from Montpellier, France. Their paper describes an original liquid-assisted ball-milling methodology for peptide bond synthesis – avoiding toxic solvents and reactants – and its application to the synthesis of Leu-enkephalin.

Read the research: Environmentally benign peptide synthesis using liquid-assisted ball-milling: application to the synthesis of Leu-enkephalin, J. Bonnamour, T.-X. Métro, J. Martinez and F. Lamaty, Green Chem., 2013, 15, 1116–1120, DOI: c3gc40302e

Both of these articles are free to access for 6 weeks!

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

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Creating biodegradable electronics using shellac

Scientists in Austria, Romania and Turkey have used the natural resin shellac to devise biocompatible organic field-effect transistors (OFETs), which could help make electronic gadgets biodegradable and allow easier use of OFETs in the body.

Multi-coloured row of nail polish bottles, illustrating a current application of shellac

© Shutterstock

Together with their better known cousins – organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs) – OFETs are already revolutionising the electronics industry, bringing us flexible displays and light-weight solar-powered chargers. Switching the synthetic substrate material and dielectric layer to the naturally occurring shellac has a number of advantages such as low cost, low toxicity and low environmental impact.

Currently used in the fashion and beauty industry as a hard-wearing nail varnish, shellac has also been used to make gramophone records and as a furniture finish. The material is composed of a mixture of aliphatic and alicyclic hydroxy acids that are easily cross-linked by heating, resulting in a smooth, glassy substrate for the OFET devices to be built upon. It is also easy to process.

 

Read the full article in Chemistry World

Read the original journal article in Green Chemistry:
Natural resin shellac as a substrate and a dielectric layer for organic field-effect transistors
Mihai Irimia-Vladu, Eric Daniel Głowacki, Günther Schwabegger, Lucia Leonat, Hava Zekiye Akpinar, Helmut Sitter, Siegfried Bauer and Niyazi Serdar Sariciftci
Green Chem., 2013, Advance Article 
DOI: 10.1039/C3GC40388B, Communication

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Sieving silica sieves from biomass ash

Burning biomass for heat and power could produce as much as 2000 TWh by 2020, which would produce 4–15.6 million tonnes of waste ash, per year, in Europe alone. To address the problem of what to do with all this waste, scientists in the UK have developed a method to convert this ash into mesoporous silica.

Although some of the waste ash produced from the combustion of biomass is currently used in construction, most of it ends up in landfill. Therefore, extracting alkali silicates, which can be used in cement, detergents, catalysts and catalyst supports, is one way of reusing the potentially huge quantities of ash due to be produced in the future.

The team, led by Duncan Maquarrie at the University of York, developed an efficient route for extracting the silicates by forming alkali silicate solutions. The silicate solutions were converted into the porous silica, MCM-41, a useful catalyst and molecular sieve.

Read what Duncan Macquarrie has to say about the research in Chemistry World.

Read the original research published in Green Chemistry:

Alkali silicates and structured mesoporous silicas from biomass power station wastes: the emergence of bio-MCMs, J. R. Dodson,  E. C. Cooper,  A. J. Hunt,  A. Matharu,  J. Cole,  A. Minihan,  J. H. Clark and D. J. Macquarrie, Green Chem., 2013, DOI: 10.1039/C3GC40324F

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Top 10 most accessed articles in January

For Green Chemistry, the top 10 most accessed articles in January were as follows:

Selective oxidation of alcohols and aldehydes over supported metal nanoparticles
Sara E. Davis, Matthew S. Ide and Robert J. Davis
Green Chem., 2013, 15, 17-45
DOI: 10.1039/C2GC36441G, Critical Review

Food waste biomass: a resource for high-value chemicals
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly Budarin and James H. Clark
Green Chem., 2013, 15, 307-314
DOI: 10.1039/C2GC36978H, Perspective

A simple metal-free catalytic sulfoxidation under visible light and air
Xiangyong Gu, Xiang Li, Yahong Chai, Qi Yang, Pixu Li and Yingming Yao
Green Chem., 2013, 15, 357-361
DOI: 10.1039/C2GC36683E, Communication

Deconstruction of lignocellulosic biomass with ionic liquids
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton
Green Chem., 2013, 15, 550-583
DOI: 10.1039/C2GC36364J, Critical Review

Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N,N-dimethylformamide
Donna S. MacMillan, Jane Murray, Helen F. Sneddon, Craig Jamieson and Allan J. B. Watson
Green Chem., 2013, 15, 596-600
DOI: 10.1039/C2GC36900A, Communication

Catalytic conversion of biomass to biofuels
David Martin Alonso, Jesse Q. Bond and James A. Dumesic
Green Chem., 2010, 12, 1493-1513
DOI: 10.1039/C004654J, Critical Review

Designing endocrine disruption out of the next generation of chemicals
T. T. Schug, R. Abagyan, B. Blumberg, T. J. Collins, D. Crews, P. L. DeFur, S. M. Dickerson, T. M. Edwards, A. C. Gore, L. J. Guillette, T. Hayes, J. J. Heindel, A. Moores, H. B. Patisaul, T. L. Tal, K. A. Thayer, L. N. Vandenberg, J. C. Warner, C. S. Watson, F. S. vom Saal, R. T. Zoeller, K. P. O’Brien and J. P. Myers
Green Chem., 2013, 15, 181-198
DOI: 10.1039/C2GC35055F, Paper

Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
David Martin Alonso, Stephanie G. Wettstein and James A. Dumesic
Green Chem., 2013, 15, 584-595
DOI: 10.1039/C3GC37065H, Critical Review

Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond
Rocío García-Álvarez, Pascale Crochet and Victorio Cadierno
Green Chem., 2013, 15, 46-66
DOI: 10.1039/C2GC36534K, Tutorial Review

Cyclometalated iridium complexes for transfer hydrogenation of carbonyl groups in water
Yawen Wei, Dong Xue, Qian Lei, Chao Wang and Jianliang Xiao
Green Chem., 2013, 15, 629-634
DOI: 10.1039/C2GC36619C, Communication

Take a look at the articles, then let us know your thoughts and comments below.

Interested in submitting your own work to Green Chemistry? You can submit online today, or email us with your ideas and suggestions.

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