Author Archive

Incredible ionic liquids: an article collection

Ionic liquids are pretty self explanatory; they are ionic materials in a liquid state. In a ‘normal’ liquid, interactions are usually governed by Van de Waals or H-bonding forces. In ionic liquids it is ionic bonding interactions which dominate, meaning ionic liquids possess some interesting and unique properties.

The field of ionic liquids grew after Paul Walden’s observations of ethylammonium nitrate in 1914,1 since then the study and use of ionic liquids has grown phenomenally, with applications in analytics, biology, electrochemistry, physical chemistry, engineering, solvents and catalysis.

The academic and industrial interest in ionic liquids has thrown up some remarkable discoveries, particularly in recent years, so to keep you up to date with latest break-through research in the field we have collected these high quality articles which are free to access!*

(more…)

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Putting Green Chemistry into Mobile Apps to Communicate Globally

Screenshot of the Green Solvents App for iPad

Screenshot of the Green Solvents App for iPad

Several new mobile applications (Apps) have been recently released for the Apple iOS platform which incorporate green chemistry concepts. This represents a highly novel way to communicate science and bring green chemistry to a bigger audience, which has not previously been appreciated. We certainly sense there is an untapped audience for these types of applications due to the large number of people who now own a mobile device across all demographics. Green Chemistry related information is generally proprietary and papers on the topic are commonly behind paywalls. Making the information freely available or at low cost is a paradigm shift.

For example, a recent consortium organized by the American Chemical Society Green Chemistry InstituteTM (ACS GCI) Pharmaceutical Roundtable1 currently involves 14 pharmaceutical companies, and has developed a solvent selection guide that is publicly available on their website in the form of a PDF file.2 We have made this solvent selection guide more accessible in the form of a free app called Green Solvents.3, 4 It is delivered as a simple structure look-up guide incorporating all of the selection criteria from the ACS GCI and, in addition, having links out to other useful resources (ChemSpider 5-7 etc.). This app, like most free apps, has a small banner advertisement which does not detract from the content of the app or its usability on a mobile device. Importantly this App was not funded by the ACS or any other organization.

Screenshot of the Open Drug Discovery Teams App for iPad

Screenshot of the Open Drug Discovery Teams App for iPad

Creating the Green Solvents app has also motivated the addition of the process mass intensity (PMI) calculation8 (which is another green chemistry feature), into the Yield101 app9. A third recently developed mobile app connected to green chemistry is the Open Drug Discovery Teams (ODDT) app10, 11. ODDT is a free mobile app intended as a research topic aggregator of science data collected from various sources on the internet such as Twitter and Google Alerts. It exists to facilitate interdisciplinary teamwork and deliver access to information that is highly relevant and focused on the topic areas of interest. Research topics include areas of chemistry and adjacent molecule-oriented biomedical sciences, with an emphasis on those which are most amenable to open research at present. We have focused on green chemistry as a topic due to its potential importance for scientists involved in drug discovery for rare and neglected diseases. There is high attrition in drug discovery, so many compounds will need to be made but only a very small fraction will make it into the clinic and, far less, into the marketplace. It is therefore important to design a green process as early as possible when the cost is lower and the quantities of chemicals made are relatively small compared to when they are dramatically scaled up for manufacturing. We feel these global neglected and rare disease researchers would benefit greatly from being informed about green chemistry principles early on and that this has not been considered by any of the major organizations driving green chemistry initiatives. This app has also been used to visualize the ACS GCI solvent selection guide in a different format as it was Tweeted out to reach an even wider audience for those following the hashtag #greenchemistry. To date we are the only researchers that have created and used mobile apps to communicate green chemistry concepts. We feel this is an area that is ripe for expansion to further educate scientists.

Sean Ekins*
Collaborations in Chemistry, 5616 Hilltop Needmore Road, Fuquay-Varina, NC 27526, U.S.A.
Alex M. Clark
Molecular Materials Informatics, 1900 St. Jacques #302, Montreal, Quebec, Canada H3J 2S1
Antony J. Williams
Royal Society of Chemistry, 904 Tamaras Circle, Wake Forest, NC 27587, U.S.A. 

1. American Chemical Society Green Chemistry InstituteTM Pharmaceutical Roundtable www.acs.org/gcipharmaroundtable
2. Solvent selection guide. http://surveys.acs.org/se.ashx?s=04BD76CC0E5496A7
3. Ekins, S. Green Solvents: From Idea to App in 3 Days. http://www.slideshare.net/ekinssean/green-solvents-app
4. Clark, A. M. Green Solvents. http://www.scimobileapps.com/index.php?title=Green_Solvents
5. ChemSpider. www.chemspider.com
6. Pence, H. E.; Williams, A. J. ChemSpider: An Online Chemical Information Resource. J Chem Educ 2010, 87, 1123-1124.
7. Williams, A. J. Public chemical compound databases. Curr Opin Drug Discov Devel 2008, 11, 393-404.
8. ACS GCI Pharmaceutical Roundtable. http://portal.acs.org/portal/acs/corg/content?_nfpb=true&_pageLabel=PP_TRANSITIONMAIN&node_id=1422&use_sec=false&sec_url_var=region1&__uuid=46aca9b6-a985-42cd-a534-7d6cabf892a7
9. Clark, A. M. Yield-101. http://www.scimobileapps.com/index.php?title=Yield101
10. Ekins, S.; Clark, A. M.; Williams, A. J. Open Drug Discovery Teams: A Chemistry Mobile App for Collaboration. Molecular Informatics 2012, In Press.
11. Philippidis, A. App connects rare disease researchers to data. http://www.genengnews.com/insight-and-intelligenceand153/app-connects-rare-disease-researchers-to-data/77899637/

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Green Chemistry Issue 11 Now Online

Issue 11 ofcGreen Chemistry Issue 11 is now online. The cover features work from Jairton Dupont and co-workers from the Universidade Federal do Rio Grande do Sul in Brazil. They show that a dicyclohexylguanidine group covalently attached on silica gel is an efficient basic heterogeneous catalyst for the production of biodiesel in a continuous flow reactor. Find out more by reading the full article ‘Silica-supported guanidine catalyst for continuous flow biodiesel production’. Issue 11 ifc

The inside front cover highlights a paper from Alexander Bismark and colleagues at Imperial College London in which frothing of acrylated epoxidised soybean oil (AESO) followed by microwave initiated polymerisation is used to make bacterial cellulose reinforced polyAESO nanocomposite foams. The introduction of Bacterial Cellulose significantly enhanced the stability of the gas-soybean oil foam templates and enhanced the mechanical properties of the polymer nanocomposite foams. Find out more by reading the full article ‘Bio-based macroporous polymer nanocomposites made by mechanical frothing of acrylated epoxidised soybean oil’.

These cover articles are free for all to access until December 15th.

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The use of environmental metrics to evaluate green chemistry improvements to synthesis

In this article the Pfizer Green Chemistry metrics program is described and, as an example of its implementation, a case history of the synthesis of (S,S)-reboxetine succinate is presented.  The environmental (and cost) improvements that were achieved through process development and synthetic route design coupled with rigorous measurement and analysis of Green Chemistry metrics are presented.

C1GC15921F(±)-Reboxetine mesylate is a selective norepinephrine uptake (NRI) inhibitor which is marketed as the racemate under the trade name Edronax for the treatment of depression.  The (S,S)-enantiomer has undergone clinical evaluation as the succinate salt for a number of indications in the pain therapeutic area. 

The initial route of synthesis to (S,S)-reboxetine succinate used a classical resolution approach and generated high levels of waste.  This route was replaced by an enantiospecific synthesis using Sharpless epoxidation chemistry, an enzymatic process to selectively protect a primary alcohol and a new efficient method of chiral morpholine construction as key steps.

These improvements reduced the levels of waste produced by more than 90%. This article describes a useful and instructive example for all scientists working in the area of green chemistry.

This article is free to access until the 30th November 2011!  To read more, please click the link below…

The use of environmental metrics to evaluate green chemistry improvements to the synthesis of (S,S)-reboxetine succinate
Georges Assaf, Graham Checksfield, Doug Critcher, Peter J. Dunn, Stuart Field, Laurence J. Harris, Roger M. Howard, Gemma Scotney, Adam Scott, Suju Mathew, Geoffrey M. H. Walker and Alexander Wilder
Green Chem., 2011, DOI: 10.1039/C1GC15921F

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Green Chemistry Volume 13 Issue 8 online now!

Green Chemistry Volume 13 Issue 8 Front Cover by Itamar Daube

Drawn by Itamar Daube; http://www.itamardaube.com

Green Chemistry issue 8 features an artist’s impression* of the problematic situation of Fischer-Tropsch bimetallic catalysis, it highlights a critical review from Advisory Board member Gadi Rothenberg and co-workers from The Netherlands and France.  Their short critical review summarises and analyses the developments in Fischer–Tropsch catalysis using bimetallic alloys, read the full article online here.

Green Chemistry Volume 13 Issue 8 Inside Front CoverThe inside front cover highlights the article ‘Controlled polymerisation of lactide using an organo-catalyst in supercritical carbon dioxide’ by Idriss Blakey and co-workers from the University of Queensland, Australia and the University of Nottingham, UK.  Their article, previously highlighted on this blog, reports the ‘green’ synthesis of well defined polylactic acid (PLA) via organo-catalysis, without using any organic solvents.  Read the full article online here.

*The copyright owner, Prof. Dr. Gadi Rothenberg, hereby gives all persons permission to use this cover image for any purpose, provided that the artist’s name and website is correctly cited.  Drawn by Itamar Daube; http://www.itamardaube.com

 
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How to design a safer chemical

Towards rational molecular design: derivation of property guidelines for reduced acute aquatic toxicity A recent Green Chemistry article from Julie Zimmerman, Paul Anastas and co-workers from Yale University and Baylor University describes guidelines which should be followed in order to design chemicals with reduced aquatic toxicity.  Their article has been highlighted in Nature News.

The team highlight that there is a need for synthetic chemists to focus on design of safer chemicals rather than testing for toxicity after production.  The team explored mechanistically-driven qualitative and quantitative analyses between the in-silico predicted molecular properties and in vivo toxicity data to propose property limits associated with higher probabilities of safe chemicals.  They propose design guidelines that can be used to significantly increase the probability that a chemical will have low toxicity to the aquatic species studied. 

Interested in knowing more? Read the full article for free until September 1st!

Towards rational molecular design: derivation of property guidelines for reduced acute aquatic toxicity
Adelina M. Voutchkova, Jakub Kostal, Justin B. Steinfeld, John W. Emerson, Bryan W. Brooks, Paul Anastas and Julie B. Zimmerman
Green Chem., 2011, DOI: 10.1039/C1GC15651A

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Granting wishes for researchers

Rafael Luque discusses funding for early stage researchers and the importance of green chemistry with Anna Simpson

Rafael Luque

Rafael Luque is the Ramon y Cajal fellow at the University of Cordoba in Spain. His interests range from materials science, nanotechnology and heterogeneous catalysis to biomass valorisation and biofuels.

How did you get to where you are today? 

I was always fascinated by chemistry because it’s in everything. This table that we are sitting at is chemistry! 

I did my undergraduate degree at the University of Cordoba in Spain and I was delighted to receive a grant to do my PhD in the organic chemistry department there. I started to have my own ideas and in pursuing them, my supervisors were always happy. It all worked out really well in the end! 

During my PhD, I spent six months at the green chemistry centre of excellence at the University of York in the UK. I worked with Duncan Macquarrie who had a big impact on my career. I am very grateful to him and to James Clark for this. After my PhD, I returned to York as a green chemistry research associate and spent some of the most wonderful years of my career to date there. Everything went very well in York; however, after three and a half years as a postdoc, I needed to move on with my career and my life. So, due to personal and family pressures, I decided to move back to Cordoba. In the beginning, this was difficult but I managed to get a nice fellowship and now have a small group of four PhD students and a postdoc starting soon. 

What are the biggest challenges facing young researchers and what’s your advice for someone about to embark on the next step after a PhD or postdoc? 

Innovation is the key to success. You can’t get grant money for doing the same thing that we have been doing for over 20 years, it must be new work. 

Getting funding and grants is challenging, but even with a very small group, such as one masters or PhD student, you can start to do more work. I have met lots of innovative and creative people in Europe and Spain. They have lots of interesting ideas and promising research but the problem is they need basic funding to progress. My advice is to keep trying and not lose courage as generally, if you are unsuccessful, you have to carry on and fight for what you want to do. 

You have quite wide ranging research interests but the theme that underpins it all is green and sustainable chemistry. Why is green chemistry important? 

Green chemistry is going to be everything in the future. We will be using green products made using technology with low environmental impact and utilising locally sourced materials and even waste. The perception of waste as a resource rather than a problem is something we have to change in people’s minds. We still have some work to do there. 

After working in both the UK and Spain, what differences did you experience between the chemical research communities in these countries? 

There are lots of differences. In the UK, there are big funding agencies to support researchers. This is something we lack in Spain, but I must stress that in Spain, I have found that we are good and very competitive in terms of publications and research. We are innovative and creative and I was very pleased to see, when I got back, that there were so many people doing such a great job – it is a big inspiration for me. It is especially apparent with young researchers. They lack resources but are still self-motivated to pursue their dreams, which is very encouraging. I take care of students and encourage them to carry on because I can see that this degree of motivation is getting them everywhere. I love teaching – there is always a way to engage the students to learn about chemistry. Being a young academic often helps because students feel closer to you as there is not an age barrier. The language and the way you communicate with the students are not so different. 

Where does your funding come from? 

At the moment it’s mostly national and regional funding. This wasn’t particularly easy to get, but the government supports young researchers with groundbreaking ideas. The funding I received is aimed at early career researchers and for me, after proposing one of these groundbreaking concepts, it was helpful that I could get some funding – it allowed me to go back to Cordoba. 

Hopefully, at the end of October, I will try my best to be successful with a European bid, which could potentially put me in a more stable situation and allow me to grow a bigger group. This funding, called a ‘Starting Research Grant’ is indeed a lot of money – 1.5 million Euros – so it could have a big impact on my career. Its purpose is to allow someone to develop ideas and start an independent research group that could lead to important developments for Europe. We plan to work with lignocellulosics and lignin, one of our main targets. 

What do you like to do when you are not doing chemistry? 

I love travelling – it’s one of my favourite things, so I have been all over the world except for Australia and New Zealand. When I’m at home, I’m addicted to video games; I must admit that I am a big fan. Other than that, I love music, so if I wasn’t a chemist I would probably be a DJ.

Read some of Rafael Luque’s latest work in Green Chemistry by following the links below:

Catalytically active self-assembled silica-based nanostructures containing supported nanoparticles
Camino Gonzalez-Arellano, Alina Mariana Balu, Rafael Luque and Duncan J. Macquarrie
Green Chem., 2010, 12, 1995-2002

Magnetically separable nanoferrite-anchored glutathione: aqueous homocoupling of arylboronic acids under microwave irradiation
Rafael Luque, Babita Baruwati and Rajender S. Varma
Green Chem., 2010, 12, 1540-1543

Highly active and selective supported iron oxide nanoparticles in microwave-assisted N-alkylations of amines with alcohols
Camino Gonzalez-Arellano, Kenta Yoshida, Rafael Luque and Pratibha L. Gai
Green Chem., 2010, 12, 1281-1287

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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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