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Meet our Authors: James Mack

James Mack is an Associate Professor of Chemistry at the University of Cincinnati, USA.  His current research is in the development of environmentally benign organic reactions and in particular mechano- or ball milling chemistry.  James took a few moments to speak to Green Chemistry

 Who or what initially inspired you to become a chemist?

 My parents bought me a chemistry set in grade school and I played with the set which included small experiments. I became more interested in high school chemistry. However, I knew when I took an organic chemistry sophomore year in college, that I would pursue a career in the field.

What has been the motivation behind your recent research?

When I was in graduate school I went to a seminar on Green Chemistry and thought there must be a better way to make more environmentally benign reactions. Also, chemistry should make life better for the next generation and I can be part of that change.

What do you see as the main challenges facing research in this area?

One of the challenges is explaining to world leaders that the chemical methodologies we use today will drastically impact the future. We can’t consistently borrow against the future. For example, we use resources today and hope to find alternatives tomorrow; we need to find better ways to conserve the resources we have.

Where do you see the field of Green Chemistry being in 5 or 10 years time?

In 5 to 10 years, the field will grow tremendously because students are more environmentally conscious than I was in my twenties. Green chemistry and protecting the environment is embedded in the social consciousness of today’s youth.

And finally…

If you could not be a scientist, but could be anything else, what would you be?

If I couldn’t be a chemist, my dream job would be to become the General Manager of the Boston Celtics (NBA basketball team). After all, it’s a green team! That would be magical and certainly a dream comes true! I also love to debate; therefore, pursuing a law degree would have been another great career choice.

Take a look a couple of James’ recent articles in Green Chemistryfree to access until the 19th June 2012:

Investigating the formation of dialkyl carbonates using high speed ball milling, Daniel C. Waddell, Indre Thiel, Ashley Bunger, Dominique Nkata, Ashley Maloney, Tammara Clark, Brandon Smith and James Mack, Green Chem., 2011, 13, 3156-3161

A two-step ball milling method synthesizes and purifies α,β-unsaturated esters, William C. Shearouse, Chelsea M. Korte and James Mack, Green Chem., 2011, 13, 598-601

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Highly-efficient conversion of glycerol to solketal over heterogeneous Lewis acid catalysts

Several mesoporous substituted silicates were applied to the acetalization of acetone with glycerol to yield solketal.

The team of scientists led by Pablo Pescarmona from KU Leuven, Belgium, illustrate for the first time that mesoporous Lewis acid catalysts can be active for this reaction to produce solketal.  Solketal is a very valuable compound with direct applications as a fuel additive, surfactant and flavouring agent.  Of the catalysts tested, the catalyst which showed the highest conversion and turnover numbers was the novel Hf-TUD-1 material.  Along with two other materials, these catalysts gave superior results compared to a reference solid acid catalyst such as Ultrastable zeolite Y.  The active materials do not suffer from leaching and could be efficiently reused in consecutive catalytic cycles.

This article is free to access until the 12th June 2012!  Click on this link below to find out more…

Highly-efficient conversion of glycerol to solketal over heterogeneous Lewis acid catalysts, Li Li, Tamás I. Korányi, Bert F. Sels and Paolo P. Pescarmona, Green Chem., 2012, DOI: 10.1039/C2GC16619D

You may also be interested in these articles – free to access for 2 weeks:

Selective conversion of trioses to lactates over Lewis acid heterogeneous catalysts, Li Li,  Christophe Stroobants, Kaifeng LinPierre A. Jacobs, Bert F. Sels and Paolo P. Pescarmona, Green Chem., 2011, 13, 1175-1181

Zeolite-catalysed conversion of C3 sugars to alkyl lactates, Paolo P. Pescarmona, Kris P. F. Janssen, Chloë Delaet, Christophe Stroobants, Kristof Houthoofd, An Philippaerts, Chantal De Jonghe, Johan S. Paul, Pierre A. Jacobs and Bert F. Sels, Green Chem., 2010, 12, 1083-1089

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GRC Green Chemistry 2012

The 2012 ‘Olympic’ Gordon Research Conference on Green Chemistrywill be held between the 22nd-27th July 2012 at the Renaissance Tuscany II Ciocco Resort in Lucca (Braga), Italy.

The conference will will present cutting-edge research and the most important advances relevant to environmentally benign and sustainable chemistry and chemical processing.  The key scientific sessions will be of interest to both industry and academia and will focus on designing greener chemicals, greener approaches to organic synthesis, catalysis and biocatalysis, polymers and materials, bio-inspired materials, energy and fuels, and assessing our progress toward a sustainable future.

The conference Chairs are Karen I. Goldberg and Steve Howdle with Vice Chairs Kenneth Seddon and Mark A. Harmer.

Applications for this meeting must be submitted by the 24th June 2012.  Please apply early and some meetings become over subscribed before this deadline.

For full details about the conference, click here.

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An environmentally friendlier approach to hydrometallurgy

Scientists from Belgium have developed an environmentally friendly route to separate cobalt from nickel, magnesium and calcium in chloride medium.

Koen Binnemans and colleagues from KU Leuven and Umicore, Belgium used undiluted phosphonium-based ionic liquids as the extractants with tri(hexyl)tetradecylphosphonium chloride (Cyphos IL 101) as the best ionic liquid tested in terms of commercial availability, separation characteristics and ease of handling.  The main advantage of their method is the fact that no organic diluents are required and thus volatile organic solvents can be avoided. The process enabled separation factors greater than 50 000 to be observed for cobalt/nickel separation.  In addition, the ionic liquid can easily be recovered and reused as extractant so there is potential for a continuous extraction process to be developed.

This article is free to access until the 6th June 2012!  Click on the link below to find out more…

An environmentally friendlier approach to hydrometallurgy: highly selective separation of cobalt from nickel by solvent extraction with undiluted phosphonium ionic liquids, Sil Wellens, Ben Thijs and Koen Binnemans, Green Chem., 2012, DOI: 10.1039/C2GC35246J

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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

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Green Solvents 2012 – Submission deadline extended to the 15th May!

The deadline for submission of abstracts for the ‘Green Solvents – Advanced Concepts for Solution Phase Chemistry and Processes‘ has been extended to the 15th May 2012.  This conference will be taking place between the 7th-10th October in picturesque Boppard, Germany.

This event is part of the biennial conference series “Green Solvents” and this year’s scientific focus lies on energy-efficient processes, selectivity control for waste prevention, alternative and efficient use of raw materials, activation and capture of CO2 and integrated reaction and separation processes.

Submit your abstract now!

For more information about the many renowned invited speakers, the topics and abstract submission, please visit: www.dechema.de/gsfs2012.

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Green Chemistry issue 5 – now online!

The latest issue of Green Chemistryissue 5 – is now published online.

The front cover of this issue features work by James Dumesic and co-workers from the University of Wisconsin-Madison, USA.  In this paper, the authors report the selective hydrogenation of biomass-derived 5-hydroxymethylfurfural using heterogeneous catalysts.  A variety of supported catalysts in monophasic and biphasic reactions systems were studied to determine the effects of the metal, support, solution phase acidity and solvent on the selectivity of the reaction.  The authors found that Ru supported on materials with high isoelectric points (e.g. ceria and γ-alumina) gave the highest yields.

The selective hydrogenation of biomass-derived 5-hydroxymethylfurfural using heterogeneous catalysts, Ricardo Alamillo, Mark Tucker, Mei Chia, Yomaira Pagán-Torres and James Dumesic, Green Chem., 2012, 14, 1413-1419

The inside front cover of this issue highlights work by Klavs Jensen and Xiaoying Liu from Massachusetts Institute of Technology, USA, who report the direct oxidative amidation of aromatic aldehydes in a continuous flow microreactor system using aqueous hydrogen peroxide.  This method allows amides to be synthesized from secondary amines and aromatic aldehydes in a single operation under mild conditions within 15-40 mins.  The procedure does not require catalysts or promoting reagents.

Direct oxidative amidation of aromatic aldehydes using aqueous hydrogen peroxide in continuous flow microreactor systems, Xiaoying Liu and Klavs F. Jensen, Green Chem., 2012, 14, 1471-1474

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2012 Berkeley Centre for Green Chemistry Conference

The BCGC 2nd Annual Conference in Green Chemistry: Collaborative Approaches and New Solutions is being held at the University of California Berkeley on the 3rd May 2012.

The Spring 2012 BCGC Green Chemistry meeting will build awareness of Green Chemistry’s growing role in education, research and outreach on and off campus.

The morning speakers will each speak to one of the Center’s core research or outreach themes: (1) Advancing legislation to incentivize greener solutions (2) Creating new catalysts for green chemical transformations, (3) Promoting greener materials selection with quantitative tools and metrics, and (4) Developing an ethics for decision making in green chemistry. 

During the afternoon session we will host two panel discussions highlighting two of our most integrated interdisciplinary initiatives at the BCGC: (1) How should we advance an interdisciplinary approach to education in green chemistry at UC Berkeley and other Universities? (2) What is the role of biobased chemicals and products in a greener market place?

Confirmed speakers at the event include: Debbie Raphael, California Department of Toxic Substances Control; John Hartwig, UC Berkeley Department of Chemistry; Lauren Heine, Cleaner Production Action; John Warner, Warner Babcock Institute for Green Chemistry; Bill Tolman, University of Minnesota Department of Chemistry; Roger McFadden, Staples, Steve Hahn, Dow Chemical and Joan Blades, Founder of MoveOn.org and MomsRising.org.

Click here to find out more…

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4th International IUPAC Conference on Green Chemistry

The 4th International IUPAC Conference on Green Chemistry (4th ICGC) will be held in Foz do Iguaçu, Brazil between the 25-29th August 2012. 

The 4th ICGC will focus on broad topics including benign synthesis/processes, green chemistry for energy production, chemicals from renewable resources, green engineering, education in green chemistry and engineering and policy.  The conference will be held in Foz do Iguaçu, one of the most beautiful tourist destinations in Latin America.

Confirmed Plenary lectaures are: Paul Anastas (Yale University, USA), James Clark (University of York, UK), Jairton Dupont (University of Rio Grande do Sul, Brazil), Buxing Han (Chinese Academy of Sciences, China), Adelio Machado (Porto University, Portugal), Anita Marsaioli (University of Campinas, Brazil), Robin Rogers (University of Alabama, USA), Karl Barry Sharpless (Scripps Research Institute, USA), Roger Sheldon (Delft University, The Netherlands) and Rajendar S. Varma (EPA, USA).

Submission of abstracts and early bird registration must be completed by the 15th May.  For more information, please visit the website.

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Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water

A supported organaocatalyst has been developed for direct asymmetric Aldol reaction in water with higher enantioselectivity than the original homogeneous catalyst.

Asymmetric organocatalyst is considered to be a very powerful tool for stereoselective synthesis on enantiomerically enriched compounds.  However, organocatalytic reactions, whilst avoiding many of the problems associated with metal catalysts, often require high catalyst loadings and tedious purification of the products. 

In this work, Roser Pleixats and colleagues from the Autonomous University of Barcelona, the University of Alicante (Spain) and the Institute Charles Gerhardt Montpellier (France), have developed a recyclable silica-supported prolinamide organocatalyst.  The catalyst was applied to the direct asymmetric Aldol reaction, and allowed reactions to be conducted exclusively in water without the need of a co-catalyst.  This also resulted in easier isolation of the product and good recycling (at least three times) of the catalyst without the need for regeneration. 

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

Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water, Amàlia Monge-Marcet, Xavier Cattoën, Diego A. Alonso, Carmen Nájera, Michel Wong Chi Man and Roser Pleixats, Green Chem., 2012, DOI: 10.1039/C2GC35227C

You may also be interested in the following article as well – free to access for 2 weeks!

Advances in catalytic metal-free reductions: from bio-inspired concepts to applications in the organocatalytic synthesis of pharmaceuticals and natural products, Magnus Rueping, Jeremy Dufour and Fenja R. Schoepke, Green Chem., 2011, 13, 1084-1105

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Meet our Authors: Pedro Lozano

Pedro Lozano in a Professor of Biochemistry and Molecular Biology at the University of Murcia, Spain.  His current research interests are related to enzyme technology with particular focus on the use of enzymes in ionic liquids and supercritical fluids.  Pedro took time out from his work to speak to Green Chemistry

Who or what initially inspired you to become a chemist?

My interest in experimental sciences began during my training at High School, which awoke my passion to know and understand all the phenomena of Nature. The choice to be a chemist was really accidental, because belonging to a family with few economic resources I had to study at the public University nearest my home, the University of Murcia. In 1979, Chemistry was the only experimental sciences degree offered this university. However, during the last two years of training in Chemistry, I chose the specialty of Biochemistry, allowing me to discover not only that the essence of life is chemistry, but also the enormous potential of applying biological systems to develop chemical processes of industrial interest in the context of Biotechnology. In fact, my PhD dealt with a cross-flow membrane reactor with immobilized pectinases to continuously produce clarified fruit juices.

What has been the motivation behind your recent research?

During the 90’s, my research was focused on the application of proteases to peptide synthesis in non-conventional media, mainly organic solvents and supercritical fluids. I came across supercritical fluids during my postdoctoral training at the Centre de Bioengenierie Gilbert Durand at Toulouse. I realized that there was a whole world to discover using biocatalytic systems in combination with these new solvents. Then by chance, in 1999 I met Dr. Michel Vaultier who was visiting the University of Murcia, and it was he who introduced me to ionic liquids. Also, the paper of Prof Joan F. Brennecke, (Nature, 1999, 399, 28-29) was a source of inspiration. Since that time, the combination of the catalytic excellence of enzymes with the unique characteristics of both supercritical fluids and ionic liquids has been a constant in my research activities. The idea of being able to perform clean and continuous catalytic processes under non-aqueous conditions using the inherent advantages of enzymes for processes of industrial interest is the final aim. At this moment, both dynamic kinetic resolutions and the enzymatic synthesis of biodiesel are the two processes under study, because of their possible application to important strategic sectors of the pharmaceutical and biofuels industries, respectively. However, the small size of our laboratory, the lack of human and material resources and an excessive teaching load are clear limitations to any research development.

What do you see as the main challenges facing research in this area?

Today, the big challenge, not only in this field, is to be able to do research in Spain in the deep economic crisis.

Outside this context, to provide a sufficiently high level of activity and stability to the enzymes to carry out synthetic processes in an overall reaction and separation approach is an important challenge. In the case of chemoenzymatic processes, it is important to have an active and selective chemical catalyst for the racemisation step, as it must also preserve (or at least, not destroy) the catalytic properties of enzymes for the kinetic resolution step. For instance, we have developed appropriate chemoenzymatic systems for the dynamic kinetic resolution of a sec-arylalcohol, but there are other sec-compounds like sec-amines, sec-thiols, etc. (in aryl and alkyl compounds), but there are many candidate reactions waiting to be studied. In the case of the enzymatic synthesis of biodiesel, our original contribution concerned the use of ILs with a large alkyl-side chain in their cations. This provides efficient monophasic reaction systems for enzyme catalysis, and opened the door to their industrial application. The full transformation of vegetable oil into biofuel molecules, without the undesirable production of glycerol is a very interesting challenge for any multicatalytic system.

Where do you see the field of Green Chemistry being in 5 or 10 years time?

The main overall challenge for the 21st century is to ensure truly sustainable development, as it is defined by the Brundtland Report, “development that meets the needs of the present without compromising the ability of future generations to meet their own need”, where the implementation of the twelve Principles of Green Chemistry, masterfully defined by Prof. Paul T. Anastas, is a good roadmap to follow. In the next 10 years, the interest of the society in green chemistry will be at its highest level, because of the profound changes that it should be occur in the chemical industry sector. Green Chemistry research should make efforts to combine selective catalysts with clean reaction media, by using sustainable approaches for product recovery and to enable the recycling/reuse of these reaction media. To transfer the exquisite efficiency shown by enzymes in nature to chemical processes may constitute the most powerful toolbox for developing a clean and sustainable chemical industry in the near future.

And finally…

If you could not be a scientist, but could be anything else, what would you be?

Really, research is vocational, and provides scientists with the enormous pleasure of having a job they enjoy. In my case, I am very lucky with my job. Furthermore, I like to work and I enjoy working…. As an undergraduate, I had many jobs during the summers to earn money to finance my studies. So, if I had not been a scientist, I do not know what other job had I would have chosen, but I am sure that it would be a job of service to society, which I would enjoy.

Take a look a couple of Pedro’s recent articles in Green Chemistryfree to access until the 22nd May 2012:

Stabilizing immobilized cellulase by ionic liquids for saccharification of cellulose solutions in 1-butyl-3-methylimidazolium chloride, Pedro Lozano, Berenice Bernal, Juana M. Bernal, Mathieu Pucheault and Michel Vaultier, Green Chem., 2011, 13, 1406-1410

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

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