Archive for the ‘News’ Category

New Impact Factor for Green Chemistry

Green Chemistry received a 5-year impact factor* of 6.056 in the 2010 Journal Citation Reports released by Thomson ISI this week.  This reveals steady growth in the impact of Green Chemistry over the last 5 years, reinforcing the importance and maturity of the Journal. 

Five years ago Green Chemistry had an impact factor of 3.255 and its 2010 impact factor of 5.472 demonstrates the Journal’s increasing quality, putting it in the top 20 of all multidisciplinary chemistry journals.

We would like to thank our Editorial and Advisory Board members and all of our authors and referees for their contributions; this support is vital to the continuing success of Green Chemistry.

The release of the 2010 impact factors also brought good news for RSC Publishing with a rise in the average impact factor across all journals and some great individual performances… read more here.

*A 5-year impact factor is the average number of times articles from a journal published in the past five years have been cited in the JCR year.  It is calculated by taking the number of citations in the JCR year to articles published in the preceding 5 years and dividing by the number of articles published in the previous 5 years.

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2011 Presidential Green Chemistry Challenge Awards

For the 16th year, the U.S. Environmental Protection Agency is recognizing pioneering chemical technologies developed by leading researchers and industrial innovators who are making significant contributions to pollution prevention in the United States. These prestigious awards recognise and promote research and development of less-hazardous alternatives to existing technologies that reduce or eliminate waste, particularly hazardous waste, in industrial production.

The Presidential Green Chemistry Challenge Awards are bestowed in five categories. Green Chemistry would like to congratulate the 2011 award winners:

  • Academic: Bruce H. Lipshutz, PhD, University of California, Santa Barbara
  • Small business: BioAmber, Inc., Plymouth, Minn.
  • Greener synthetic pathways: Genomatica, San Diego, Calif.
  • Greener reaction conditions: Kraton Performance Polymers, Inc., Houston, Texas
  • Designing greener chemicals: The Sherwin-Williams Company, Cleveland, Ohio

The awards were made on Monday night, June 20th at the Green Chemistry Challenge Awards ceremony in Washington D.C. as an opener to the 15th Annual Green Chemistry & Engineering Conference which is being held in concert with the 5th International Conference on Green & Sustainable Chemistry.

Green Chemistry Editor Sarah Ruthven is in Washington D.C. attending the Conferences; if you would like to meet her there please contact the Editorial Office.

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Green Solvents for Synthesis Conference Report

Conference report by Ewa Gebauer-Henke and Mark Muldoon 

The latest issue of Green Chemistry features papers from the “Green Solvents for Synthesis” conference that was held in October 2010. The bi-annual DECHEMA conference on green solvents has a reputation for attracting world leaders in the field of green chemistry and also for being held in beautiful locations in Germany. In 2008, the meeting was held in Friedrichshafen on Lake Constance, while this recent meeting was in the stunning town of Berchtesgaden in the German Bavarian Alps. 

Berchtesgaden

Berchtesgaden

Common themes throughout the conference were the use of ionic liquids, water, supercritical fluids (CO2 and water), CO2 expanded solvent systems and solvents from renewable sources. The meeting attracted a mix of industrialists, academics and graduate students from across the globe. Addressing the challenges in this area requires an interdisciplinary approach and attendees had a wide range of scientific and engineering backgrounds. The varied nature of the research presented at this meeting is clear from the contributions to this special issue. For those interested, the full conference programme can still be viewed online

One of the things that seemed clear from the discussions and debates among participants was that this field is continuing to mature and strive for higher standards. Many of the discussions related to improving the overall greenness of processes and topics such as “life cycle analysis” and “energy” were often raised. The claim that a solvent is intrinsically green in itself is not something that holds up to scrutiny and therefore researchers are having to demonstrate how solvents can be used to improve a process overall; for example by allowing catalyst separation and recycling or delivering improved reaction rates and product selectivity. 

The first lecture of the conference by Philip Jessop highlighted many of these issues and set the tone for the meeting. He outlined what he felt were the four “grand challenges” in the field of green solvents. Additionally, he had polled some of the leading academic researchers in the field of solvents prior to the conference, asking them what solvents they felt would have the biggest impact in the coming years. He then discussed the interesting results of this survey during his talk. The details of his lecture can be seen in his paper “Searching for green Solvents”. 

Ionic liquids have gathered a great deal of interest in the last decade or so and a number of talks highlighted how these solvents can be used to improve the greenness of a process. For example, Peter Wasserscheid delivered a very well received talk on the topic of ionic liquids in the field of heterogeneous catalysis. He discussed both SILP (“Supported Ionic Liquid Phase”) technology and SCILLs (Solid Catalysts with Ionic Iiquid Layers’).  For a number of years, researchers have been investigating the use of SILPs; which involves utilising a thin ionic liquid layer on a solid support to immobilise homogeneous transition metal catalysts. However, more recently, the SCILL approach has emerged, and this involves coating a “traditional” heterogeneous type catalyst with a layer of ionic liquid. The layer of ionic liquid can result in modification of the properties and performance of the heterogeneous catalyst. Peter’s talk illustrated well how ionic liquids could improve catalyst performance, therefore leading to a greener process.   

The conference chairman Prof Walter Leitner

The conference chairman Prof Walter Leitner

Continuous flow is often the best way to improve the efficiency of a process and “alternative solvent systems” can enable flow processes to be developed in ways not possible with conventional organic solvents. For example, Pedro Lozano described his group’s work on continuous flow enzymatic synthesis of biodiesel in mono- and multiphase systems using a combination of ionic liquids and supercritical CO2. While Lasse Greiner discussed the application of continuous flow systems for the synthesis of ionic liquids. He stressed how the transition from batch to continuous is only possible, when kinetic and thermodynamic studies have been carried out and showed how inline ATR-IR and calorimetry were powerful tools for such studies.  He demonstrated that the synthesis of ionic liquids can be realized with consistent product specifications; necessary in large scale production. 

The importance of in-situ techniques was also highlighted in Jan-Dierk Grunwald’s talk “Heterogeneous catalysis in dense carbon dioxide: opportunities, limitations and mechanistic understanding”.  He presented work on both catalytic hydrogenations and oxidations in dense and supercritical CO2. As part of these studies, ATR-IR was used to determine phase behaviour and X-ray adsorption spectroscopy to study the catalyst under high pressure reaction conditions. Developing an in-depth understanding of reactions in such solvents is important if they are to be fully exploited in an industrial setting. 

Ultimately, the aim of green chemistry is to have an impact in the real world and there are an increasing number of industrial processes that now utilise “alternative solvent” technologies. Several examples were highlighted during this conference including those that exploited supercritical water. This was particularly nice to see as this is a solvent system that is often labelled as an academic curiosity. More details of industrial scale processes for scH2O are described in the paper by Adschiri and co-workers. 

Solvents play a crucial role to vast number of processes and they are therefore key in developing more sustainable chemical processes. We would highly recommend that researchers interested in the important area of green chemistry attend a future DECHEMA green solvents conference. The next one is scheduled for early October 2012 (and starts just as Oktoberfest in finishing in Munich). As mentioned, these meetings bring together leaders from academia and industry from across a range of disciplines. In fact many of these leading figures not only discuss their research but also entertain the participants! At this past it closed with a traditional Bavarian banquet dinner where some very well known academics entertained the attendees singing that Leitner and Howdle classic “Always Use Green Chemistry Tools”; something, previously highlighted by Kathleen Too in this blog (October 15th entry). 

Ewa Gebauer-Henke
CAT Catalytic Center Postdoctoral Fellow
ITMC, RWTH Aachen University 

Mark Muldoon
School of Chemistry and Chemical Engineering
Queen’s University Belfast

Pictures, courtesy of Prof Kenneth Seddon (QUILL, Queen’s University of Belfast)

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Green Chemistry Board Members are RSC Prize Winners

Poliakoff 120

Professor Martyn Poliakoff

The RSC Prize Winners 2011 have recently been announced and Green Chemistry Board Members Martyn Poliakoff and James Clark have both been honoured.  The RSC Prizes have been designed to be of the broadest relevance to the chemical sciences community as a whole, rewarding those whose careers are defined by exceptional work, excellence and dedication. 

Professor Martyn Poliakoff from Nottingham University is Chair of the Green Chemistry Editorial Board.  He was recently nominated to be the next Foreign Secretary of the Royal Society. Professor Poliakoff has been awarded the Nyholm Prize for Education which is for outstanding accomplishment in education relating to the chemical sciences.  He was chosen due to his enthusiastic leadership in taking chemistry to the widest possible audience, using not only traditional channels but also the power of YouTube.

Professor James Clark

Professor James Clark

Professor James Clark was the founding Editor of Green Chemistry and is still involved with the journal on our Advisory Board.  He has been awarded the Environment Prize which is for outstanding contributions to the chemical sciences in the area of environment, sustainability and energy (sponsored by Proctor & Gamble).  Professor Clark was chosen for his fundamental and applied research contributions to the areas of green chemistry, clean technology and sustainability and for educational, publishing and public awareness contributions in the green chemistry area.

We would like to congratulate Professor Poliakoff and Professor Clark.

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Top ten most accessed articles in April

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

Expanding GSK’s solvent selection guide – embedding sustainability into solvent selection starting at medicinal chemistry 
Richard K. Henderson, Concepción Jiménez-González, David J. C. Constable, Sarah R. Alston, Graham G. A. Inglis, Gail Fisher, James Sherwood, Steve P. Binks and Alan D. Curzons 
Green Chem., 2011, 13, 854-862 DOI: 10.1039/C0GC00918K, Paper 

5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications 
Andreia A. Rosatella, Svilen P. Simeonov, Raquel F. M. Frade and Carlos A. M. Afonso 
Green Chem., 2011, 13, 754-793 DOI: 10.1039/C0GC00401D, Critical Review 

Greener solvents for ruthenium and palladium-catalysed aromatic C-H bond functionalisation 
Cedric Fischmeister and Henri Doucet 
Green Chem., 2011, 13, 741-753 DOI: 10.1039/C0GC00885K  

Searching for green solvents
Philip G. Jessop 
Green Chem., 2011, Advance Article DOI: 10.1039/C0GC00797H, Perspective 

Algae as a source of renewable chemicals: opportunities and challenges 
Patrick M. Foley, Evan S. Beach and Julie B. Zimmerman 
Green Chem., 2011, Advance Article DOI: 10.1039/C1GC00015B  

A critical assessment of the greenness and energy efficiency of microwave-assisted organic synthesis 
Jonathan D. Moseley and C. Oliver Kappe 
Green Chem., 2011, 13, 794-806 DOI: 10.1039/C0GC00823K, Perspective 

One-pot preparation of magnetic N-heterocyclic carbene-functionalized silica nanoparticles for the Suzuki-Miyaura coupling of aryl chlorides: improved activity and facile catalyst recovery 
Hengquan Yang, Yunwei Wang, Yong Qin, Yanzhu Chong, Qiaozhen Yang, Guang Li, Li Zhang and Wei Li 
Green Chem., 2011, 13, 1352-1361 DOI: 10.1039/C0GC00955E  

The 13 Principles of Green Chemistry and Engineering for a Greener Africa 
Nigist Asfaw, Yonas Chebude, Andinet Ejigu, Bitu B. Hurisso, Peter Licence, Richard L. Smith, Samantha L. Y. Tang and Martyn Poliakoff 
Green Chem., 2011, 13, 1059-1060 DOI: 10.1039/C0GC00936A  

Viable methodologies for the synthesis of high-quality nanostructures 
Jonathan M. Patete, Xiaohui Peng, Christopher Koenigsmann, Yan Xu, Barbara Karn and Stanislaus S. Wong 
Green Chem., 2011, 13, 482-519 DOI: 10.1039/C0GC00516A, Critical Review 

Production of liquid hydrocarbon fuels by catalytic conversion of biomass-derived levulinic acid 
Drew J. Braden, Carlos A. Henao, Jacob Heltzel, Christos C. Maravelias and James A. Dumesic 
Green Chem., 2011, Advance Article DOI: 10.1039/C1GC15047B  

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 Editorial Board Chair Martyn Poliakoff nominated as Foreign Secretary of the Royal Society

Martyn Poliakoff CBE FRS

Martyn Poliakoff CBE FRS

Professor Martyn Poliakoff CBE has been nominated as the next Foreign Secretary of the Royal Society. Professor Poliakoff is the Chair of the Green Chemistry Editorial Board.

Foreign Secretary of the Royal Society is one of its most prestigious positions and the holder is responsible for building relationships around the world, particularly with other scientific academies, and ensuring that British Science and the Royal Society is recognised and promoted internationally. The post dates back to 1723 – predating the post of Foreign Secretary in the UK government by sixty years.

The appointment will not be official until the 7th of July when a ballot will be held and Fellows of the Royal Society asked to indicate their support, however, in keeping with tradition Professor Poliakoff is the only nominee.

As well as his duties for Green Chemistry, Professor Poliakoff is Research Professor of Chemistry at the University of Nottingham and one of the developers and regular presenters of the YouTube channel The Periodic Table of Videos where you can view a video in which Professor Poliakoff explains more about this appointment.  You can also read a recent interview with Professor Poliakoff on the Green Chemistry blog.

Professor Poliakoff’s current research interests involve chemical applications of supercritical fluids, with particular emphasis on green chemistry, and a selection of his most recent Green Chemistry articles have been made free until the 7th of July when his post will be made official.

The 13 Principles of Green Chemistry and Engineering for a Greener Africa
Nigist Asfaw, Yonas Chebude, Andinet Ejigu, Bitu B. Hurisso, Peter Licence, Richard L. Smith, Samantha L. Y. Tang and Martyn Poliakoff
Green Chem., 2011, 13, 1059-1060, DOI: 10.1039/C0GC00936A, Editorial

Continuous heterogeneous catalytic oxidation of primary and secondary alcohols in scCO2
Adrian O. Chapman, Geoffrey R. Akien, Nicholas J. Arrowsmith, Peter Licence and Martyn Poliakoff
Green Chem., 2010, 12, 310-315, DOI: 10.1039/B913434D, Paper

Solubilisation of α-chymotrypsin by hydrophobic ion pairing in fluorous systems and supercritical carbon dioxide and demonstration of efficient enzyme recycling
Karima Benaissi, Martyn Poliakoff and Neil R. Thomas
Green Chem., 2010, 12, 54-59, DOI: 10.1039/B904761A, Paper

Strategies for cleaner oxidations using photochemically generated singlet oxygen in supercritical carbon dioxide
Xue Han, Richard A. Bourne, Martyn Poliakoff and Michael W. George
Green Chem., 2009, 11, 1787-1792, DOI: 10.1039/B914074C, Paper

A critical look at reactions in class I and II gas-expanded liquids using CO2 and other gases
Geoffrey R. Akien and Martyn Poliakoff
Green Chem., 2009, 11, 1083-1100, DOI: 10.1039/B904097H, Critical Review

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Top ten most accessed articles in March

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

Converting carbohydrates to bulk chemicals and fine chemicals over heterogeneous catalysts 
Maria J. Climent, Avelino Corma and Sara Iborra 
Green Chem., 2011, 13, 520-540 DOI: 10.1039/C0GC00639D, Critical Review 

5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications 
Andreia A. Rosatella, Svilen P. Simeonov, Raquel F. M. Frade and Carlos A. M. Afonso 
Green Chem., 2011, 13, 754-793 DOI: 10.1039/C0GC00401D, Critical Review 

Expanding GSK’s solvent selection guide – embedding sustainability into solvent selection starting at medicinal chemistry 
Richard K. Henderson, Concepción Jiménez-González, David J. C. Constable, Sarah R. Alston, Graham G. A. Inglis, Gail Fisher, James Sherwood, Steve P. Binks and Alan D. Curzons 
Green Chem., 2011, 13, 854-862 DOI: 10.1039/C0GC00918K, Paper 

Viable methodologies for the synthesis of high-quality nanostructures 
Jonathan M. Patete, Xiaohui Peng, Christopher Koenigsmann, Yan Xu, Barbara Karn and Stanislaus S. Wong 
Green Chem., 2011, 13, 482-519 DOI: 10.1039/C0GC00516A, Critical Review 

Synthesis of highly stable dispersions of nanosized copper particles using l-ascorbic acid 
Jing Xiong, Ye Wang, Qunji Xue and Xuedong Wu 
Green Chem., 2011, 13, 900-904 DOI: 10.1039/C0GC00772B, Paper 

The irruption of polymers from renewable resources on the scene of macromolecular science and technology 
Alessandro Gandini 
Green Chem., 2011, Advance Article DOI: 10.1039/C0GC00789G, Critical Review 

A critical assessment of the greenness and energy efficiency of microwave-assisted organic synthesis 
Jonathan D. Moseley and C. Oliver Kappe 
Green Chem., 2011, 13, 794-806 DOI: 10.1039/C0GC00823K, Perspective 

Searching for green solvents 
Philip G. Jessop 
Green Chem., 2011, Advance Article DOI: 10.1039/C0GC00797H, Perspective 

A simple and efficient protocol for a palladium-catalyzed ligand-free Suzuki reaction at room temperature in aqueous DMF 
Chun Liu, Qijian Ni, Fanying Bao and Jieshan Qiu 
Green Chem., 2011, Advance Article DOI: 10.1039/C0GC00176G, Paper 

Processing of metals and metal oxides using ionic liquids 
Andrew P. Abbott, Gero Frisch, Jennifer Hartley and Karl S. Ryder 
Green Chem., 2011, 13, 471-481 DOI: 10.1039/C0GC00716A, Critical Review 

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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Top ten most accessed articles in February

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

Searching for green solvents 
Philip G. Jessop 
Green Chem., 2011, Advance Article, DOI: 10.1039/C0GC00797H, Perspective 

Enzyme-mediated oxidations for the chemist 
Frank Hollmann, Isabel W. C. E. Arends, Katja Buehler, Anett Schallmey and Bruno Bühler 
Green Chem., 2011, 13, 226-265, DOI: 10.1039/C0GC00595A, Critical Review 

Greener solvents for ruthenium and palladium-catalysed aromatic C-H bond functionalisation 
Cedric Fischmeister and Henri Doucet 
Green Chem., 2011, Advance Article, DOI: 10.1039/C0GC00885K, Critical Review 

Synthesis of highly stable dispersions of nanosized copper particles using l-ascorbic acid 
Jing Xiong, Ye Wang, Qunji Xue and Xuedong Wu 
Green Chem., 2011, Advance Article, DOI: 10.1039/C0GC00772B, Paper 

Tertiary amine solvents having switchable hydrophilicity 
Philip G. Jessop, Lisa Kozycz, Zahra Ghoshouni Rahami, Dylan Schoenmakers, Alaina R. Boyd, Dominik Wechsler and Amy M. Holland 
Green Chem., 2011, 13, 619-623, DOI: 10.1039/C0GC00806K, Paper 

Supported ionic liquid silica nanoparticles (SILnPs) as an efficient and recyclable heterogeneous catalyst for the dehydration of fructose to 5-hydroxymethylfurfural 
Kalpesh B. Sidhpuria, Ana L. Daniel-da-Silva, Tito Trindade and João A. P. Coutinho 
Green Chem., 2011, 13, 340-349, DOI: 10.1039/C0GC00690D, Paper 

Synthesis of sugar alcohols by hydrolytic hydrogenation of cellulose over supported metal catalysts 
Hirokazu Kobayashi, Yukiko Ito, Tasuku Komanoya, Yuto Hosaka, Paresh L. Dhepe, Koji Kasai, Kenji Hara and Atsushi Fukuoka 
Green Chem., 2011, 13, 326-333, DOI: 10.1039/C0GC00666A, Paper 

CuCl-catalyzed green oxidative alkyne homocoupling without palladium, ligands and bases 
Kun Yin, Chunju Li, Jian Li and Xueshun Jia 
Green Chem., 2011, 13, 591-593, DOI: 10.1039/C0GC00413H, Communication 

An efficient activity ionic liquid-enzyme system for biodiesel production 
Teresa De Diego, Arturo Manjón, Pedro Lozano, Michel Vaultier and José L. Iborra 
Green Chem., 2011, 13, 444-451, DOI: 10.1039/C0GC00230E, Paper 

Converting carbohydrates to bulk chemicals and fine chemicals over heterogeneous catalysts 
Maria J. Climent, Avelino Corma and Sara Iborra 
Green Chem., 2011, 13, 520-540, DOI: 10.1039/C0GC00639D, Critical Review 

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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Top ten most accessed articles in January

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

Converting carbohydrates to bulk chemicals and fine chemicals over heterogeneous catalysts 
Maria J. Climent, Avelino Corma and Sara Iborra 
Green Chem., 2011, 13, 520-540, DOI: 10.1039/C0GC00639D, Critical Review 

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, DOI: 10.1039/C0GC00685H, Tutorial Review 

Use of carbon dioxide in chemical syntheses via a lactone intermediate 
A. Behr and G. Henze 
Green Chem., 2011, 13, 25-39, DOI: 10.1039/C0GC00394H, Critical Review 

Supported ionic liquid silica nanoparticles (SILnPs) as an efficient and recyclable heterogeneous catalyst for the dehydration of fructose to 5-hydroxymethylfurfural 
Kalpesh B. Sidhpuria, Ana L. Daniel-da-Silva, Tito Trindade and João A. P. Coutinho 
Green Chem., 2011, 13, 340-349, DOI: 10.1039/C0GC00690D, Paper 

Oxidation of 5-hydroxymethylfurfural to maleic anhydride with molecular oxygen 
Zhongtian Du, Jiping Ma, Feng Wang, Junxia Liu and Jie Xu 
Green Chem., 2011, 13, 554-557, DOI: 10.1039/C0GC00837K, Communication 

Synergy of boric acid and added salts in the catalytic dehydration of hexoses to 5-hydroxymethylfurfural in water 
Thomas S. Hansen, Jerrik Mielby and Anders Riisager 
Green Chem., 2011, 13, 109-114 DOI: 10.1039/C0GC00355G, Paper 

Viable methodologies for the synthesis of high-quality nanostructures 
Jonathan M. Patete, Xiaohui Peng, Christopher Koenigsmann, Yan Xu, Barbara Karn and Stanislaus S. Wong 
Green Chem., 2011, 13, 482-519, DOI: 10.1039/C0GC00516A, Critical Review 

A green protocol for palladium-catalysed Suzuki-Miyaura cross-coupling 
Alexander N. Marziale, Dominik Jantke, Stefan H. Faul, Thomas Reiner, Eberhardt Herdtweck and Jörg Eppinger 
Green Chem., 2011, 13, 169-177, DOI: 10.1039/C0GC00522C, Paper 

Synthesis of the natural herbicide d-aminolevulinic acid from cellulose-derived 5-(chloromethyl)furfural 
Mark Mascal and Saikat Dutta 
Green Chem., 2011, 13, 40-41, DOI: 10.1039/C0GC00548G, Communication 

Microwave-assisted solvent- and ligand-free copper-catalysed cross-coupling between halopyridines and nitrogen nucleophiles 
Zhen-Jiang Liu, Jean-Pierre Vors, Ernst R. F. Gesing and Carsten Bolm 
Green Chem., 2011, 13, 42-45, DOI: 10.1039/C0GC00296H, Communication 

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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New editorial policy on the publication of Ionic Liquid studies in Green Chemistry

“Not all ionic liquids are green!” is what we often hear at Green Chemistry conferences. Indeed there have been many debates about ionic liquid toxicity and more importantly how we determine if an ionic liquid is “green”. However, we increasingly receive a number of articles merely reporting the properties of an ionic liquid or its toxicity with no insight on its impact on green processes.

In the new editorial by Tom Welton, he clarifies the Journal’s policy on the publication of ionic liquid toxicity studies. While it is, of course, a very important area of research for the ionic liquid community, the new guidelines in the editorial state that articles purely on ionic liquid toxicity will no longer fall within the scope of Green Chemistry. However,  if an article on ionic liquid toxicity demonstrates that the design of the ionic liquid improves a green process or product then that article is within the redefined scope of the Journal. In the same way that studies on the physical properties of ionic liquids are useful to practitioners of Green Chemistry, the actual work in itself is not “green chemistry” – the same applies to ionic liquid toxicity studies.

Click here to read the full editorial by Tom Welton.

Whether it is an ionic liquid or not, choosing the right solvent is very important when attempting to make a chemical process “greener”. Read the latest perspective by Phil Jessop on searching for green solvents.

Is the green solvents research community investing time and effort in the areas of research that will give the maximum environmental benefit? What areas of research would increase the benefit?
Philip G. Jessop
Green Chem., 2011, Advance Article, DOI: 10.1039/C0GC00797H, Perspective

 

You may also be interested in reading our 2009 themed issue on “Green solvents – Progress in science and application” published in Green Chemistry.

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