Archive for the ‘News’ Category

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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Top ten most accessed articles in December

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

Glycerol dehydration to acrolein in the context of new uses of glycerol 
Benjamin Katryniok, Sébastien Paul, Virginie Bellière-Baca, Patrick Rey and Franck Dumeignil 
Green Chem., 2010, 12, 2079-2098, DOI: 10.1039/C0GC00307G, Critical Review 

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, Advance Article, DOI: 10.1039/C0GC00666A, Paper 

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 

Synthesis of thermoplastic starch mixed esters catalyzed by the in situ generation of imidazolium salts 
André Lehmann, Bert Volkert, Mehdi Hassan-Nejad, Tonino Greco and Hans-Peter Fink 
Green Chem., 2010, 12, 2164-2171, DOI: 10.1039/C0GC00366B, Paper 

ß-cyclodextrin catalysed synthesis of tryptanthrin in water 
Atul Kumar, Vishwa Deepak Tripathi and Promod Kumar 
Green Chem., 2011, 13, 51-54, DOI: 10.1039/C0GC00523A, Communication 

Eco-friendly liquid chromatographic separations based on the use of cyclodextrins as mobile phase additives 
Víctor González-Ruiz, Andrés G. León, Ana I. Olives, M. Antonia Martín and J. Carlos Menéndez 
Green Chem., 2011, 13, 115-126, DOI: 10.1039/C0GC00456A, Paper 

An efficient copper-catalysed aerobic oxybromination of arenes in water 
Jian Wang, Wei Wang and Jing-Hua Li 
Green Chem., 2010, 12, 2124-2126, DOI: 10.1039/C0GC00328J, Communication 

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 

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 

Selective hydrogenolysis of biomass-derived xylitol to ethylene glycol and propylene glycol on supported Ru catalysts 
Jiying Sun and Haichao Liu 
Green Chem., 2011, 13, 135-142, DOI: 10.1039/C0GC00571A, Paper 

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 November

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

Vegetable oil-based polymeric materials: synthesis, properties, and applications 
Ying Xia and Richard C. Larock 
Green Chem., 2010, 12, 1893-1909, DOI: 10.1039/C0GC00264J, Critical Review 

Production of jet and diesel fuel range alkanes from waste hemicellulose-derived aqueous solutions 
Rong Xing, Ayyagari V. Subrahmanyam, Hakan Olcay, Wei Qi, G. Peter van Walsum, Hemant Pendse and George W. Huber 
Green Chem., 2010, 12, 1933-1946, DOI: 10.1039/C0GC00263A, Paper 

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 

A solid-acid-based process for the conversion of hemicellulose 
Paresh Laxmikant Dhepe and Ramakanta Sahu 
Green Chem., 2010, 12, 2153-2156, DOI: 10.1039/C004128A, Communication 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570-573, DOI: 10.1039/B920000B, Communication 

Glycerol dehydration to acrolein in the context of new uses of glycerol 
Benjamin Katryniok, Sébastien Paul, Virginie Bellière-Baca, Patrick Rey and Franck Dumeignil 
Green Chem., 2010, 12, 2079-2098, DOI: 10.1039/C0GC00307G, Critical Review 

A silica gel supported dual acidic ionic liquid: an efficient and recyclable heterogeneous catalyst for the one-pot synthesis of amidoalkyl naphthols 
Qiang Zhang, Jun Luo and Yunyang Wei 
Green Chem., 2010, 12, 2246-2254, DOI: 10.1039/C0GC00472C, Paper 

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 

Efficient copper-catalyzed N-arylations of nitrogen-containing heterocycles and aliphatic amines in water 
Xufeng Li, Daoshan Yang, Yuyang Jiang and Hua Fu 
Green Chem., 2010, 12, 1097-1105, DOI: 10.1039/C002172E, Paper 

Highly efficient catalyst for the decarbonylation of lactic acid to acetaldehyde 
Benjamin Katryniok, Sébastien Paul and Franck Dumeignil 
Green Chem., 2010, 12, 1910-1913, DOI: 10.1039/C0GC00203H, 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 Associate Editor for Green Chemistry

Professor Chao-Jun Li

We are delighted to announce that Professor Chao-Jun Li (McGill University, Canada) is the new Associate Editor for Green Chemistry.

His main area of research is innovative and fundamentally new organic reactions that will defy conventional reactivities and possess high “atom-efficiency”.

Professor Li will handle manuscripts from the Americas and Canada and his editorial office is now open for submissions. We welcome Professor Li to this new role.

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Lights, camera, action

Martyn Poliakoff, CBE, FRS, is research professor of chemistry at the University of Nottingham in the UK. His main research interest is the application of supercritical fluids with a focus on green and sustainable chemistry. He is one of the narrators of 'The Periodic Table of Videos', which are popular on YouTube. He is chair of the Green Chemistry editorial board.

Martyn Poliakoff talks to Kathleen Too about the periodic table of videos and passion for green chemistry

Can you tell us a little known fact about yourself? 

I’m an Honorary Professor at Moscow State University, something I share with Fidel Castro and Bill Clinton. 

Which of your academic achievements are you most proud of? 

To me, academic work is rather like journalism – journalists get excited about the story they are working on, but when they move on to the next story, that one is more exciting than the one before. So I think that the only way you can operate as an academic is to be excited about whatever you are doing at a particular time. When I was younger, I did a lot of work on the reactive molecule iron tetracarbonyl, which is completely useless in the green chemistry context because it only exists at room temperature for a millionth of a second or less , but I am still quite proud of my experiments. As a professor, I am proud of the little contributions I can make to the design of an experiment by my research group. Experiments are almost always done by my students or postdocs. Sometimes, as a supervisor, the contributions to the design of the experiments are not as big as one would like. Occasionally, I have a really good idea , which makes the experiments work and that always give me pleasure. 

You’re keen to promote science on YouTube. Could you tell us more? 

I began working with YouTube purely by accident. My university was collaborating with Brady Haran, a very talented video journalist, who wanted to make a periodic table of videos. I didn’t think there was enough to say about some of the more obscure elements but as it turned out, there was plenty to say, at least enough to make short videos. We wanted to show that we enjoy chemistry and how much fun it can be. 

We’re in the process of making videos about different molecules and reactions. There are also other videos that are rather difficult to define, for example, we made a video of gold dissolving in Aqua Regia – a mixture of nitric acid and hydrochloric acid – it’s not exactly a reaction or a molecule but we thought that people may be interested in seeing the gold dissolving. 

Which video was the most fun to make? 

They were all fun, but my favourite is about the element hassium. This is element 108 and I knew nothing about it. In fact, in the precredit sequence – the bit before the main title of the video – I was filmed saying ‘I don’t know anything about hassium, let’s make something up’. 

What is your favourite element? 

I’m very fond of sodium. The chemical symbol for sodium is Na, which was my mother’s nickname when she was a child. Each time I hear the word Na or see it written down, I get a warm feeling. I’m also fond of xenon, because it’s been an important element in my research. 

What excites you about chemistry and what does the future hold for green chemistry? 

Objects we use in everyday life, such as most of the clothes we wear, are made from synthetic chemicals. The jacket I’m wearing is actually leather but the inside is made of polyester – a synthetic material. We couldn’t enjoy any of these without the products of the chemical industry. Chemistry often has a bad image. People generally think about it polluting and destroying the planet but green chemistry allows young people to feel that they are helping both the planet and humanity at the same time. So it’s doubly good! 

With oil running out and the expanding world population leading to a greater demand for chemicals, we have got to do something. One of the greatest challenges is to get green chemistry to work. The future either holds success in delivering what people need or complete failure leading to society collapsing. We have to succeed. I hope that in the end the principles of green chemistry will be applied to most chemistry. You could argue that if green chemistry really succeeds, it will disappear because all chemistry will become green. 

What do you enjoy most about being the chair of Green Chemistry? 

I enjoy interacting with other chemists, inspiring young people and spreading the green chemistry message. I also enjoy promoting the subject in Ethiopia and encouraging people in economically developing countries to take up green chemistry so that they don’t make the same mistakes regarding pollution that we did in the past. 

What advice do you have for young scientists? 

Green chemistry offers terrific opportunities and there are different areas within the subject. It doesn’t matter that some people are using ionic liquids, others using new catalysts, the important message is that green chemistry is not about one area being better than another. We need all those areas and many more to solve our current problems. One of the attractions of green chemistry is that there are huge opportunities for new ideas. 

Which historical scientific figure would you most like to have dinner with and why? 

I have been fortunate to have met many fascinating famous scientists. One of the exciting things is actually finding out what they are like as people and not just learning about what they have discovered. However, historical figures come from a very different age. Possibly, they would strike us as being pompous or very formal compared to nowadays, not because they were famous scientists but because they lived 100 or 200 years ago. From my point of view, there are two quite exciting events that happened in 1869. One was Mendeleev propounding the Periodic Table for the first time. The other was that Thomas Andrews, a physical chemist in Belfast, described the critical point of carbon dioxide for the first time. Supercritical fluids have played a very important part in my research. It’s quite amusing that the two events took place in the same year. I would quite like to have dinner with Thomas Andrews and Mendeleev, though of course, they might not have been able to speak to each other because I am not sure whether Mendeleev could speak English. He definitely spoke German because he published some of his papers in German. It probably would be a rather strange triangular conversation. 

How would your family and friends describe you? 

Always doing chemistry.

When you got your CBE, how was your meeting with the Royal Family? 

A CBE is a British Award, which stands for Commander of the Order of the British Empire. It is presented at Buckingham Palace by a member of the Royal Family. I met with Prince Charles and he was very interested in my work. We had a 45 second discussion about recycling plastics, which was quite unexpected. He really had done his homework! 

You already have a number of fans; you even have a Martyn Poliakoff appreciation society on Facebook. How do you feel about being famous and how do you deal with fame? 

I’m not sure that I’m particularly famous. My brother is a well known playwright in the UK and much better known than me. Ten years ago I was walking through Helsinki with a friend of mine, who is very well known in Finland. I was with him and my postdoc who asked, ‘Have you noticed that everybody is looking at Neil?’ I replied ‘No’, because I am used to people staring at my hair anyway. So I didn’t notice anything different. 

Articles of interests:

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
DOI:10.1039/b913434d

Solubilisation of -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
DOI:10.1039/b904761a

Videos of interests:

Link icon The Periodic Table of Videos – Sodium
The Periodic Table of Videos – Sodium

Link icon The Periodic Table of Videos – Xenon
The Periodic Table of Videos – Xenon

Link icon The Periodic Table of Videos – Hassium
The Periodic Table of Videos – Hassium

Link icon Dissolving gold in aqua regia
Dissolving gold in aqua regia

Link icon Chemistry Christmas Tree
Chemistry Christmas Tree

Link icon Which element for Christmas?
Which element for Christmas?

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Top ten most accessed articles in October

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

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  

Vegetable oil-based polymeric materials: synthesis, properties, and applications 
Ying Xia and Richard C. Larock 
Green Chem., 2010, 12, 1893-1909, DOI: 10.1039/C0GC00264J, Critical Review  

Production of jet and diesel fuel range alkanes from waste hemicellulose-derived aqueous solutions 
Rong Xing, Ayyagari V. Subrahmanyam, Hakan Olcay, Wei Qi, G. Peter van Walsum, Hemant Pendse and George W. Huber 
Green Chem., 2010, 12, 1933-1946, DOI: 10.1039/C0GC00263A, Paper  

Sulfonated silica/carbon nanocomposites as novel catalysts for hydrolysis of cellulose to glucose 
Stijn Van de Vyver, Li Peng, Jan Geboers, Hans Schepers, Filip de Clippel, Cedric J. Gommes, Bart Goderis, Pierre A. Jacobs and Bert F. Sels 
Green Chem., 2010, 12, 1560-1563, DOI: 10.1039/C0GC00235F, Communication  

Heterogeneous catalytic synthesis using microreactor technology 
Christopher G. Frost and Lynsey Mutton 
Green Chem., 2010, 12, 1687-1703, DOI: 10.1039/C0GC00133C, Tutorial Review 

Biorenewable polyethylene terephthalate mimics derived from lignin and acetic acid 
Laurent Mialon, Alexander G. Pemba and Stephen A. Miller 
Green Chem., 2010, 12, 1704-1706, DOI: 10.1039/C0GC00150C, Communication 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570-573, DOI: 10.1039/B920000B, Communication  

Mild water-promoted selective deacetalisatison of acyclic acetals 
D. Bradley G. Williams, Adam Cullen, Alex Fourie, Hendrik Henning, Michelle Lawton, Wayne Mommsen, Portia Nangu, Jonathan Parker and Alicia Renison 
Green Chem., 2010, 12, 1919-1921, DOI: 10.1039/C0GC00280A, Communication  

Sulfated tungstate: a new solid heterogeneous catalyst for amide synthesis 
Pramod S. Chaudhari, Suresh D. Salim, Ravindra V. Sawant and Krishnacharya G. Akamanchi 
Green Chem., 2010, 12, 1707-1710, DOI: 10.1039/C0GC00053A, Communication 

Liquid phase oxidation of p-xylene to terephthalic acid at medium-high temperatures: multiple benefits of CO2-expanded liquids 
Xiaobin Zuo, Fenghui Niu, Kirk Snavely, Bala Subramaniam and Daryle H. Busch 
Green Chem., 2010, 12, 260-267, DOI: 10.1039/B920262E, Paper  

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 September

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

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 

Sulfonated silica/carbon nanocomposites as novel catalysts for hydrolysis of cellulose to glucose 
Stijn Van de Vyver, Li Peng, Jan Geboers, Hans Schepers, Filip de Clippel, Cedric J. Gommes, Bart Goderis, Pierre A. Jacobs and Bert F. Sels 
Green Chem., 2010, 12, 1560-1563, DOI: 10.1039/C0GC00235F , Communication 

Synthesis of cyclic carbonates from epoxides and CO2 
Michael North, Riccardo Pasquale and Carl Young 
Green Chem., 2010, 12, 1514-1539, DOI: 10.1039/C0GC00065E , Critical Review 

Fe3O4 nanoparticles: a robust and magnetically recoverable catalyst for three-component coupling of aldehyde, alkyne and amine 
Tieqiang Zeng, Wen-Wen Chen, Ciprian M. Cirtiu, Audrey Moores, Gonghua Song and Chao-Jun Li 
Green Chem., 2010, 12, 570-573, DOI: 10.1039/B920000B , Communication 

Switchable adhesives for carpet tiles: a major breakthrough in sustainable flooring 
Peter S. Shuttleworth, James H. Clark, Robert Mantle and Nigel Stansfield 
Green Chem., 2010, 12, 798-803, DOI: 10.1039/B922735K , Paper 

Liquid phase oxidation of p-xylene to terephthalic acid at medium-high temperatures: multiple benefits of CO2-expanded liquids 
Xiaobin Zuo, Fenghui Niu, Kirk Snavely, Bala Subramaniam and Daryle H. Busch 
Green Chem., 2010, 12, 260-267, DOI: 10.1039/B920262E , Paper 

Pausing a stir: heterogeneous catalysis in “dry water” 
Benjamin O. Carter, Dave J. Adams and Andrew I. Cooper 
Green Chem., 2010, 12, 783-785, DOI: 10.1039/B922508K , Communication 

A solvent having switchable hydrophilicity 
Philip G. Jessop, Lam Phan, Andrew Carrier, Shona Robinson, Christoph J. Dürr and Jitendra R. Harjani 
Green Chem., 2010, 12, 809-814, DOI: 10.1039/B926885E , Paper 

Production of liquid hydrocarbon transportation fuels by oligomerization of biomass-derived C9 alkenes 
David Martin Alonso, Jesse Q. Bond, Juan Carlos Serrano-Ruiz and James A. Dumesic 
Green Chem., 2010, 12, 992-999, DOI: 10.1039/C001899F , Paper 

Catalytic disassembly of an organosolv lignin via hydrogen transfer from supercritical methanol 
Katalin Barta, Theodore D. Matson, Makayla L. Fettig, Susannah L. Scott, Alexei V. Iretskii and Peter C. Ford 
Green Chem., 2010, 12, 1640-1647, DOI: 10.1039/C0GC00181C , Paper 

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