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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

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

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Green Solvents 2012 – Submission deadline extended to the 30th April 2012!

The latest event in the biennial ‘Green Solvents for Synthesis‘ conference series is being held on the 7th-10th October 2012 in Boppard, Germany – Advanced Concepts for Solution Phase Chemistry and Processes.

The submission deadline for abstracts for oral and poster presentations has now been extended to the 30th April 2012!  To submit your abstract or for more details, please click here.

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.

The scientific programme features the traditional Sunday evening lecture, keynote lectures by renowned experts in the field and submitted oral presentations.  An additional highlight is the poster session which will give you the opportunity for gripping discussions on cutting-edge research results.

More information can be found at the conference website: http://events.dechema.de/events/en/gsfs2012.html.  Registration for the event will open by the end of June.

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RSC US Roadshows 2012 – Week 1: California

As week 1 of the RSC US Raodshows 2012 begins, look out for Green Chemistry Editor Sarah Ruthven who will be visiting universities in California this week.

Starting on the 16th April, RSC Publishing will be touring the United States of America to share more than 170 years experience of publishing in the chemical sciences. Sixteen universities across the country will be hosting these one-day events, which are open to all members of the hosting institute.

Week 1 sees RSC Publishing visit four universities in California:

  • 16th AprilUniversity of California Irvine
  • 17th AprilUniversity of California Los Angeles
  • 18th AprilUniversity of California Santa Barbara
  • 20th AprilUniversity of California Berkeley

Click here to find out more…

Keep up to date with the RSC US roadshow by following the Royal Society of Chemistry on Facebook, or look out for #RSC2012 on Twitter!

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Green Chemistry issue 4 now online!

The latest issue of Green Chemistry is now available online!

The front cover highlights work by Milton Hearn and colleagues from Monash University, Australia, who investigated the oxidative N-demethylation of tropane alkaloids to their nortropane derivatives using hydrogen peroxide (H2O2) and an iron (III) tetraamido macrocycle catalyst.  The tertiary N-methylamine group is commonly found in a range of naturally occurring alkaloids, and modification of this tertiary amine group on tropane alkaloids alters their pharmacological properties. Previous methods for removing this methyl group tend to involve the use of large molar excess of expensive and/or toxic reagents.  The method reported by Hearn and his team uses a relatively benign oxidising reagent that can be easily decomposed to innocuous products once the reaction is complete.

One-pot oxidative N-demethylation of tropane alkaloids with hydrogen peroxide and a FeIII-TAML catalyst, Duy D. Do Pham, Geoffrey F. Kelso, Yuanzhong Yang and Milton T. W. Hearn, Green Chem., 2012, 14, 1189-1195

The inside front cover features work by Ana Rodríguez and co-workers from the University of Santiago de Compostela and the University of Vigo, Spain, who report on the duel role of surfactants in microalga cell lysis for the extraction of antioxidants.  The integrated process proposed uses non-ionic surfactants as cell disruptors and organic extractants of intracellular antioxidants.  The viability of the process was checked using real samples which yielded higher antioxidant activity than that provided by a traditional ultrasound-based method. 

On the double role of surfactants as microalga cell lysis agents and antioxidants extractants, G. Ulloa, C. Coutens, M. Sánchez, J. Sineiro, J. Fábregas, F. J. Deive, A. Rodríguez and M. J. Núñez, Green Chem., 2012, 14, 1044-1051

These articles will be free to access for 6 weeks!

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

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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:-

How do the fine chemical, pharmaceutical, and related industries approach green chemistry and sustainability?
William J. W. Watson
Green Chem., 2012, 14, 251-259, DOI: 10.1039/C1GC15904F

Transition metal based catalysts in the aerobic oxidation of alcohols
Camilla Parmeggiani and Francesca Cardona
Green Chem., 2012, 14, 547-564, DOI: 10.1039/C2GC16344F

Selective extraction of natural products with benign solvents and recovery by organophilic pervaporation: fractionation of d-limonene from orange peels
Prashant S. Kulkarni, Carla Brazinha, Carlos A. M. Afonso and João G. Crespo
Green Chem., 2010, 12, 1990-1994, DOI: 10.1039/C0GC00339E

Copper-catalyzed highly efficient aerobic oxidative synthesis of imines from alcohols and amines
Qiang Kang and Yugen Zhang
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16548A

Energy-efficient extraction of fuel and chemical feedstocks from algae
Rodrigo E. Teixeira
Green Chem., 2012, 14, 419-427, DOI: 10.1039/C2GC16225C

Industrial commitment to green and sustainable chemistry: using renewable materials & developing eco-friendly processes and ingredients in cosmetics
Michel Philippe, Blaise Didillon and Laurent Gilbert
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16341A

Magnetic copper-iron nanoparticles as simple heterogeneous catalysts for the azide-alkyne click reaction in water
Reuben Hudson, Chao-Jun Li and Audrey Moores
Green Chem., 2012, 14, 622-624, DOI: 10.1039/C2GC16421C

CeO2-catalysed one-pot selective synthesis of esters from nitriles and alcohols
Masazumi Tamura, Takuya Tonomura, Ken-ichi Shimizu and Atsushi Satsuma
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16424H

l-Proline catalysed multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction under solvent-free conditions
Atul Kumar, Maneesh Kumar Gupta and Mukesh Kumar
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC16297G

Conversion of carbohydrates and lignocellulosic biomass into 5-hydroxymethylfurfural using AlCl3·6H2O catalyst in a biphasic solvent system
Yu Yang, Chang-wei Hu and Mahdi M. Abu-Omar
Green Chem., 2012, 14, 509-513, DOI: 10.1039/C1GC15972K

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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Salt modified starch: sustainable, recyclable plastics

Utilization of starch as a recyclable plastic has been achieved giving a flexible plastic with mechanical properties similar to oil derived plastics.

Currently, the search for biodegradable polymers from sustainable resources has mainly focused on polylactic acid (PLA).  However, compared to petroleum based plastics, the cost of PLA is still high.  Starch as a highly abundant and sustainable material is an attractive alternative to PLA, but extensive hydrogen bonding between chains makes the plasticisation of starch difficult. 

In this work, Andrew Abbott and colleagues from the University of Leicester, UK, show that incorporation of a simple quaternary ammonium salt can overcome this problem and lead to a flexible plastic with mechanical properties similar to oil-derived plastics.  A transparent material can be produced by compression moulding which has a mechanical strength similar to polyolefin plastics.  These samples were also shown to be recyclable, losing little of their original properties.

This article is free to access until the 13th April 2012!  Click on the link below to find out more…

Salt modified starch: sustainable, recyclable plastics, Andrew P. Abbott, Andrew D. Ballantyne, Jesus Palenzuela Conde, Karl S. Ryder and William R. Wise, Green Chem., 2012, DOI: 10.1039/C2GC16568F

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Designer solvent hits hospital superbug

Scientists from Ireland, the Czech Republic and Spain have found an antimicrobial ionic liquid that targets MRSA (methicillin-resistant Staphylococcus aureus).  MRSA has made headlines in recent years as a superbug that is resistant to most standard antibiotics. The superbug is common in hospitals where patients have open wounds and weakened immune systems and at its peak, it was said to have caused 1652 deaths in the UK in 2006.

Research into finding potential antibiotic drugs against MRSA is ongoing, with many drugs currently being tested in clinical trials. Nicholas Gathergood, from Dublin City University, and colleagues, have prepared imidazolium-based ionic liquids from amino acid esters and dipeptidyl side chains as the building blocks. They tested the ionic liquids’ toxicity and found that the majority were non-toxic to microbes but two of them were highly toxic to Gram-positive bacteria, including MRSA. The two toxic compounds possessed a phenylalanine motif adjacent to the cation core. However, an analogue with a phenylalanine-phenylalanine sequence, an ionic liquid with increased lipophilicity, was less active (with no MRSA selectivity). A general trend in antimicrobial toxicity of ionic liquids is increased toxicity with increased lipophilicity. The compounds also passed ecotoxicity tests that show that they can be classed as biodegradable.

superbug MRSA
The hospital superbug MRSA is resistant to most standard antibiotics. Ionic liquids combine green chemistry and medicinal chemistry in a new way to fight it

Read the full story in Chemistry World

Link to journal article
Antimicrobial toxicity studies of ionic liquids leading to a ‘hit’ MRSA selective antibacterial imidazolium salt
Deborah Coleman ,  Marcel Špulák ,  M. Teresa Garcia and Nicholas Gathergood
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16090K

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Green Chemistry issue 3 now online

The latest issue of Green Chemistry is now online!

The front cover of this issue highlights work by Yong Huang (Peking University, China) and Hong Shen (Merck Research Laboratories, New Jersey, USA) and colleagues who report the synthesis of medicinally useful heterocycles such as pyridazinones and dihydropyrimidinones through a mild and highly efficient one-pot triple cascade procedure.  The cascade involves a Claisen-decarboxylation, an electrophilic reaction and subsequent heterocyclisation.  Indazoles and benzofurans could also be constructed through a double cascade reaction. 

One-pot synthesis of useful heterocycles in medicinal chemistry using a cascade strategy, Guiyong Wu, Weiyu Yin, Hong C. Shen and Yong Huang, Green Chem., 2012, 14, 580-585

The inside front cover features a Tutorial Review by Camilla Parmeggiani and Francesca Cardona from the University of Florence, Italy on transition metal based catalysts for the aerobic oxidation of alcohols.  The review covers advances in this area over the last 15 years, looking at transition metal catalysts in their various forms, i.e.homogeneous, heterogeneous or nanoparticles. 

Transition metal based catalysts in the aerobic oxidation of alcohols, Camilla Parmeggiani and Francesca Cardona, Green Chem., 2012, 14, 547-564

These articles have been made free to access for 6 weeks!

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

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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:-

Continuous flow reactors: a perspective
Charlotte Wiles and Paul Watts
Green Chem., 2012, 14, 38-54, DOI: 10.1039/C1GC16022B

How do the fine chemical, pharmaceutical, and related industries approach green chemistry and sustainability?
William J. W. Watson
Green Chem., 2012, 14, 251-259, DOI: 10.1039/C1GC15904F

Energy-efficient extraction of fuel and chemical feedstocks from algae
Rodrigo E. Teixeira
Green Chem., 2012, 14, 419-427, DOI: 10.1039/C2GC16225C

Environmentally benign synthesis of heterocyclic compounds by combined microwave-assisted heterogeneous catalytic approaches
Arif Daştan, Aditya Kulkarni and Béla Török
Green Chem., 2012, 14, 17-37, DOI: 10.1039/C1GC15837F

Chitosan functionalized ionic liquid as a recyclable biopolymer-supported catalyst for cycloaddition of CO2
Jian Sun, Jinquan Wang, Weiguo Cheng, Jianxin Zhang, Xiaohua Li, Suojiang Zhang and Yuanbin She
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16335G

Poly(ethylene glycol)-functionalized imidazolium salts-palladium-catalyzed Suzuki reaction in water
Ning Liu, Chun Liu and Zilin Jin
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC16486H

Highly efficient conversion of carbon dioxide catalyzed by polyethylene glycol-functionalized basic ionic liquids
Zhen-Zhen Yang ,  Ya-Nan Zhao ,  Liang-Nian He ,  Jian Gao and Zhong-Shu Yin
Green Chem., 2012, 14, 519-527, DOI: 10.1039/C2GC16039K

DABCO-Promoted three-component regioselective synthesis of functionalized chromen-5-ones and pyrano[3,2-c]chromen-5-ones via direct annulation of a-oxoketene-N,S-arylaminoacetals under solvent-free conditions
Maya Shankar Singh, Ganesh Chandra Nandi and Subhasis Samai
Green Chem., 2012, 14, 447-455, DOI: 10.1039/C1GC16129F

L-Proline catalysed multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction under solvent-free conditions
Atul Kumar, Maneesh Kumar Gupta and Mukesh Kumar
Green Chem., 2012, Advance Article, DOI: 10.1039/C1GC16297G

A sustainable process for the production of γ-valerolactone by hydrogenation of biomass-derived levulinic acid
Anna Maria Raspolli Galletti, Claudia Antonetti, Valentina De Luise and Marco Martinelli
Green Chem., 2012, Advance Article, DOI: 10.1039/C2GC15872H

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 Chair receives two more scientific acolades

Professor Martyn Poliakoff from the University of Nottingham and Chair of the Green Chemistry Editorial Board, has been awarded the Royal Society of Chemistry’s Nyholm Prize for Education and has been elected as a foreign member of the Russian Academy of Sciences.

The Nyholm Prize for Education, in honour of Sir Ronald Hyholm, has been awarded to Professor Poliakoff for his work in bringing a whole new audience to chemistry through the Periodic Table of Videos.  Professor Poliakoff said:

“I was really happy to be awarded the Nyholm Prize which I regard as a prize for the whole of the Periodic Table of Videos team. It is particularly gratifying as Sir Ronald Nyholm, in whose honour this prize is named, was a hugely important figure in both chemical research and chemical education.”

Professor Poliakoff will present a talk entitled ‘From Test Tube to YouTube’ at the RSC Education Division Nyholm Symposium at the University of Nottingham on Wednesday the 8th February. 

Professor Poliakoff has also been elected as a foreign member of the Russian Academy of Sciences, an honour which is particularly special due to his own strong links with the country. 

Green Chemistry would like to extend our warmest congratulations to Professor Poliakoff.

 

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