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	<title>Green Chemistry Blog</title>
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	<link>http://blogs.rsc.org/gc</link>
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		<title>17th Annual Green Chemistry &amp; Engineering Conference – Sustainable Chemistry &amp; Engineering in the 21st Century</title>
		<link>http://blogs.rsc.org/gc/2013/05/23/17th-annual-green-chemistry-engineering-conference-%e2%80%93-sustainable-chemistry-engineering-in-the-21st-century/</link>
		<comments>http://blogs.rsc.org/gc/2013/05/23/17th-annual-green-chemistry-engineering-conference-%e2%80%93-sustainable-chemistry-engineering-in-the-21st-century/#comments</comments>
		<pubDate>Thu, 23 May 2013 09:25:51 +0000</pubDate>
		<dc:creator>Emma Eley, Development Editor</dc:creator>
				<category><![CDATA[Conference]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2769</guid>
		<description><![CDATA[The ACS Green Chemistry Institute®’s Green Chemistry &#38; Engineering Conference (GC&#38;E) will be held on the 18–20 June 2013 in North Bethesda, Maryland, just outside of Washington DC. This event is an opportunity for scientists, businesses, students and educators, and advocates to broaden their understanding of green chemistry and engineering while building valuable connections with [...]]]></description>
			<content:encoded><![CDATA[<p><img class="size-medium wp-image-2770 alignright" title="GCANDE Banner for ACS GCI" src="http://blogs.rsc.org/gc/files/2013/05/GCANDE-Banner-for-ACS-GCI-300x137.jpg" alt="" width="346" height="152" />The ACS Green Chemistry Institute<sup>®</sup>’s <a href="http://www.gcande.org/"><strong>Green Chemistry &amp; Engineering Conference</strong></a> (GC&amp;E) will be held on the <strong>18–20 June 2013</strong> in North Bethesda, Maryland, just outside of Washington DC. This event is an opportunity for scientists, businesses, students and educators, and advocates to broaden their understanding of green chemistry and engineering while building valuable connections with leaders in this growing field.</p>
<p>GC&amp;E features three days of programming including world-renowned speakers, three poster sessions and more than 30 technical sessions on subjects such as designing safer chemicals and products, green chemistry education, and new business through green chemistry innovations.</p>
<p><strong>Conference Highlights</strong></p>
<p style="padding-left: 30px"><strong>• Daily Keynotes Speakers: </strong> There will be a daily keynote presentation from Dr. Milton Hearn, Associate-Director, Green Chemical Futures-Industry; Dr. Michael J. Pcolinski, Vice President of Innovation &amp; Technology, BASF Corporation; and Dr. Jim Hutchison, Professor of Chemistry, University of Oregon.</p>
<p style="padding-left: 30px"><strong><strong>• </strong>GC&amp;E Student Workshop: </strong>This pre-conference workshop will be Monday, 17 June 2013 and is free to students registered for the conference. Lead by ACS Green Chemistry Institute® Director, Dr. David Constable, and other experts, this workshop will be a fast pasted, interactive series of sessions covering each of the 12 Principles of Green Chemistry.</p>
<p style="padding-left: 30px"><strong><strong>• </strong>ACS Careers Workshop: </strong>On Wednesday, 19 June 2013, expert consultants from ACS Careers will conduct a 4-hour workshop to help attendees accelerate professional development. Learn more about planning and résumé preparation, maintaining an effective job search, reviewing employment trends, and enhancing professional skills.</p>
<p style="padding-left: 30px"><strong><strong>• </strong>Online Session: </strong>A special session <strong>“Global Supplies for Chemical Feedstocks in the 21st Century” </strong>will be held on Tuesday, 18 June 2013 at 7:00 p.m. EDT (–4 GMT) and <a href="http://gcande.org/hybrid/">streamed live online</a> for free to viewers around the world.</p>
<p style="padding-left: 30px"><strong><strong>• </strong>The Green Expo: </strong>The expo features vendors from business, government, and academia. Explore some of the 21<sup>st</sup> Century’s latest technology, resources, and marketplace opportunities.</p>
<p>For more information and to register, please visit the website <a href="http://www.gcande.org/">www.gcande.org</a>.</p>
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		<title>Top 10 most accessed articles in February</title>
		<link>http://blogs.rsc.org/gc/2013/05/08/top-10-most-accessed-articles-in-february/</link>
		<comments>http://blogs.rsc.org/gc/2013/05/08/top-10-most-accessed-articles-in-february/#comments</comments>
		<pubDate>Wed, 08 May 2013 09:00:57 +0000</pubDate>
		<dc:creator>Bethany Johnson</dc:creator>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2762</guid>
		<description><![CDATA[For Green Chemistry, the top 10 most accessed articles in February were as follows:
Deconstruction of lignocellulosic biomass with ionic liquids
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton  
Green Chem., 2013, 15, 550-583
DOI: 10.1039/C2GC36364J, Critical Review
Iron-catalyzed direct alkenylation of sp3(C–H) bonds via decarboxylation of cinnamic acids under ligand-free conditions
Hailong Yang, Hong Yan, Peng Sun, Yan [...]]]></description>
			<content:encoded><![CDATA[<p>For <a href="http://pubs.rsc.org/en/journals/journalissues/gc#!issueid=gc015005&amp;type=current&amp;issnprint=1463-9262" target="_blank"><em>Green Chemistry</em></a>, the top 10 most accessed articles in February were as follows:</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36364j" target="_blank">Deconstruction of lignocellulosic biomass with ionic liquids</a><br />
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton  <br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 550-583<br />
<strong>DOI</strong>: 10.1039/C2GC36364J, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c3gc37131j" target="_blank">Iron-catalyzed direct alkenylation of sp3(C–H) bonds via decarboxylation of cinnamic acids under ligand-free conditions</a><br />
Hailong Yang, Hong Yan, Peng Sun, Yan Zhu, Linhua Lu, Defu Liu, Guangwei Rong and Jincheng Mao  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 976-981<br />
<strong>DOI</strong>: 10.1039/C3GC37131J, Paper</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36525a" target="_blank">Glycerol carbonate as a versatile building block for tomorrow: synthesis, reactivity, properties and applications</a><br />
Matthieu O. Sonnati, Sonia Amigoni, Elisabeth P. Taffin de Givenchy, Thierry Darmanin, Olivier Choulet and Frédéric Guittard  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 283-306<br />
<strong>DOI</strong>: 10.1039/C2GC36525A, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36978h" target="_blank">Food waste biomass: a resource for high-value chemicals</a><br />
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly Budarin and James H. Clark  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 307-314<br />
<strong>DOI</strong>: 10.1039/C2GC36978H, Perspective</p>
<p><a href="http://dx.doi.org/10.1039/c3gc36881e" target="_blank">Ohmic heating as a new efficient process for organic synthesis in water</a><br />
Joana Pinto, Vera L. M. Silva, Ana M. G. Silva, Artur M. S. Silva, José C. S. Costa, Luís M. N. B. F. Santos, Roger Enes, José A. S. Cavaleiro, António A. M. O. S. Vicente and José A. C. Teixeira  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 970-975<br />
<strong>DOI</strong>: 10.1039/C3GC36881E, Paper</p>
<p><a href="http://dx.doi.org/10.1039/c3gc37065h" target="_blank">Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass </a><br />
David Martin Alonso, Stephanie G. Wettstein and James A. Dumesic  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 584-595<br />
<strong>DOI</strong>: 10.1039/C3GC37065H, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c3gc37047j" target="_blank">Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions</a><br />
Maya Shankar Singh, Anugula Nagaraju, Girijesh Kumar Verma, Gaurav Shukla, Rajiv Kumar Verma, Abhijeet Srivastava and Keshav Raghuvanshi  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 954-962<br />
<strong>DOI</strong>: 10.1039/C3GC37047J, Paper</p>
<p><a href="http://dx.doi.org/10.1039/c3gc36944g" target="_blank">Catalytic etherification of glycerol with short chain alkyl alcohols in the presence of Lewis acids</a><br />
Fei Liu, Karine De Oliveira Vigier, Marc Pera-Titus, Yannick Pouilloux, Jean-Marc Clacens, Floryan Decampo and François Jérôme  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 901-909<br />
<strong>DOI</strong>: 10.1039/C3GC36944G, Paper</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36441g" target="_blank">Selective oxidation of alcohols and aldehydes over supported metal nanoparticles</a><br />
Sara E. Davis, Matthew S. Ide and Robert J. Davis  <br />
<strong><em>Green Chem</em></strong>., 2013, <strong>15</strong>, 17-45<br />
<strong>DOI</strong>: 10.1039/C2GC36441G, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc35635j" target="_blank">Multicomponent reactions in unconventional solvents: state of the art<br />
</a>Yanlong Gu  <br />
<strong><em>Green Chem</em></strong>., 2012, <strong>14</strong>, 2091-2128<br />
<strong>DOI</strong>: 10.1039/C2GC35635J, Critical Review<br />
Take a look at the articles, and then let us know your thoughts and comments below.</p>
<p>Fancy submitting your own work to <a href="http://www.rsc.org/Publishing/Journals/guidelines/AuthorGuidelines/JournalPolicy/index.asp" target="_blank"><em>Green Chemistry</em></a>? You can submit <a href="http://mc.manuscriptcentral.com/rsc" target="_blank">online</a> today, or <a href="mailto:green-rsc@rsc.org" target="_blank">email us</a> with your ideas and suggestions.</p>
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		<title>Green Chemistry issue 5 now available online!</title>
		<link>http://blogs.rsc.org/gc/2013/04/30/green-chemistry-issue-5-now-available-online/</link>
		<comments>http://blogs.rsc.org/gc/2013/04/30/green-chemistry-issue-5-now-available-online/#comments</comments>
		<pubDate>Tue, 30 Apr 2013 10:25:53 +0000</pubDate>
		<dc:creator>Emma Eley, Development Editor</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2741</guid>
		<description><![CDATA[
Issue 5 of Green Chemistry is now available to read online.
The front cover (left) this month features work by Etienne Grau and Stefan Mecking from Konstanz, Germany. In their work, caryophyllene and humulene, renewable sesquiterpenes from clove oil, were subject to metathesis polymerization to yield non-crosslinked linear polymers with unique microstructures and low glass transition temperatures.
Read [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blogs.rsc.org/gc/files/2013/04/GC015005_ofc_800.jpg"><img class="alignleft size-medium wp-image-2742" title="GC015005_ofc_800" src="http://blogs.rsc.org/gc/files/2013/04/GC015005_ofc_800-229x300.jpg" alt="" width="160" height="217" /></a></p>
<p><a href="http://pubs.rsc.org/en/journals/journalissues/gc#!issueid=gc015005&amp;type=current&amp;issnprint=1463-9262"><strong>Issue 5</strong></a> of <em>Green Chemistry</em> is now available to read online.</p>
<p>The front cover (left) this month features work by <strong><span style="color: #339966">Etienne Grau</span></strong> and <strong><span style="color: #339966">Stefan Mecking </span></strong>from Konstanz, Germany. In their work, caryophyllene and humulene, renewable sesquiterpenes from clove oil, were subject to metathesis polymerization to yield non-crosslinked linear polymers with unique microstructures and low glass transition temperatures.</p>
<p>Read the research: <a href="http://xlink.rsc.org/?doi=10.1039/c3gc40300a"><strong>Polyterpenes by ring opening metathesis polymerization of caryophyllene and humulene</strong></a>, E. Grau and S. Mecking, <em>Green Chem.</em>, 2013, <strong>15</strong>, 1112–1115<a href="http://blogs.rsc.org/gc/files/2013/04/GC015005_ifc_800.jpg"><img class="alignright size-medium wp-image-2743" title="GC015005_ifc_800" src="http://blogs.rsc.org/gc/files/2013/04/GC015005_ifc_800-229x300.jpg" alt="" width="171" height="221" /></a>, <strong>DOI: c3gc40300a</strong></p>
<p>The inside front cover (right) this month features work by <span style="color: #339966"><strong>Thomas-Xavier Métro</strong></span>, <span style="color: #339966"><strong>Frédéric Lamaty </strong></span>and co-workers from Montpellier, France. Their paper describes an original liquid-assisted ball-milling methodology for peptide bond synthesis &#8211; avoiding toxic solvents and reactants &#8211; and its application to the synthesis of Leu-enkephalin.</p>
<p>Read the research: <a href="http://xlink.rsc.org/?doi=10.1039/c3gc40302e"><strong>Environmentally benign peptide synthesis using liquid-assisted ball-milling: application to the synthesis of Leu-enkephalin</strong></a>, J. Bonnamour, T.-X. Métro, J. Martinez and F. Lamaty, <em>Green Chem.</em>, 2013, <strong>15</strong>, 1116–1120, <strong>DOI: c3gc40302e</strong></p>
<p><strong>Both of these articles are free to access for <span style="text-decoration: underline">6 weeks</span>!</strong></p>
<p><strong>Keep up-to-date with the latest content in <em>Green Chemistry</em> by </strong><a href="http://www.rsc.org/Publishing/Journals/forms/V5profile.asp" target="_blank"><strong>registering</strong></a><strong> for our free table of contents alerts.</strong></p>
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		<title>Creating biodegradable electronics using shellac</title>
		<link>http://blogs.rsc.org/gc/2013/04/25/creating-biodegradable-electronics-using-shellac/</link>
		<comments>http://blogs.rsc.org/gc/2013/04/25/creating-biodegradable-electronics-using-shellac/#comments</comments>
		<pubDate>Thu, 25 Apr 2013 10:13:19 +0000</pubDate>
		<dc:creator>Bethany Johnson</dc:creator>
				<category><![CDATA[Hot Article]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2719</guid>
		<description><![CDATA[Scientists in Austria, Romania and Turkey have used the natural resin shellac to devise biocompatible organic field-effect transistors (OFETs), which could help make electronic gadgets biodegradable and allow easier use of OFETs in the body.
Together with their better known cousins – organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs) – OFETs are already revolutionising the [...]]]></description>
			<content:encoded><![CDATA[<p>Scientists in Austria, Romania and Turkey have used the <a href="http://xlink.rsc.org/?doi=10.1039/c3gc40388b">natural resin shellac to devise biocompatible organic field-effect transistors (OFETs)</a>, which could help make electronic gadgets biodegradable and allow easier use of OFETs in the body.</p>
<div class="wp-caption alignleft" style="width: 229px"><img class=" " style="border: black 1px solid" title="Shellac" src="http://www.rsc.org/chemistryworld/sites/default/files/upload/nail-varnish-bottles_shutterstock_114712771_300.jpg" alt="Multi-coloured row of nail polish bottles, illustrating a current application of shellac" width="219" height="165" /><p class="wp-caption-text">© Shutterstock</p></div>
<p>Together with their better known cousins – organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs) – OFETs are already revolutionising the electronics industry, bringing us flexible displays and light-weight solar-powered chargers. Switching the synthetic substrate material and dielectric layer to the naturally occurring shellac has a number of advantages such as low cost, low toxicity and low environmental impact.</p>
<p style="padding-left: 30px">Currently used in the fashion and beauty industry as a hard-wearing nail varnish, shellac has also been used to make gramophone records and as a furniture finish. The material is composed of a mixture of aliphatic and alicyclic hydroxy acids that are easily cross-linked by heating, resulting in a smooth, glassy substrate for the OFET devices to be built upon. It is also easy to process.</p>
<p style="text-align: left"> </p>
<p style="text-align: left">Read the <strong><a href="http://www.rsc.org/chemistryworld/2013/04/shellac-biodegradable-electronics-organic-field-effect-transistors-ofets" target="_blank">full article</a></strong> in <strong><em>Chemistry World</em></strong></p>
<p>Read the original journal article in <strong><em>Green Chemistry</em></strong>:<br />
<a href="http://xlink.rsc.org/?doi=10.1039/c3gc40388b" target="_blank">Natural resin shellac as a substrate and a dielectric layer for organic field-effect transistors<br />
</a>Mihai Irimia-Vladu, Eric Daniel Głowacki, Günther Schwabegger, Lucia Leonat, Hava Zekiye Akpinar, Helmut Sitter, Siegfried Bauer and Niyazi Serdar Sariciftci<br />
<em><strong>Green Chem.,</strong></em> 2013, Advance Article <br />
<strong>DOI</strong>: 10.1039/C3GC40388B, Communication</p>
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		<title>Sieving silica sieves from biomass ash</title>
		<link>http://blogs.rsc.org/gc/2013/04/18/sieving-silica-sieves-from-biomass-ash/</link>
		<comments>http://blogs.rsc.org/gc/2013/04/18/sieving-silica-sieves-from-biomass-ash/#comments</comments>
		<pubDate>Thu, 18 Apr 2013 08:52:15 +0000</pubDate>
		<dc:creator>Emma Eley, Development Editor</dc:creator>
				<category><![CDATA[Hot Article]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2709</guid>
		<description><![CDATA[Burning biomass for heat and power could produce as much as 2000 TWh by 2020, which would produce 4–15.6 million tonnes of waste ash, per year, in Europe alone. To address the problem of what to do with all this waste, scientists in the UK have developed a method to convert this ash into mesoporous [...]]]></description>
			<content:encoded><![CDATA[<p>Burning biomass for heat and power could produce as much as 2000 TWh by 2020, which would produce 4–15.6 million tonnes of waste ash, per year, in Europe alone. To address the problem of what to do with all this waste, scientists in the UK have developed <a href="http://xlink.rsc.org/?doi=10.1039/c3gc40324f">a method to convert this ash into mesoporous silica</a>.</p>
<p><img class="alignright" title="© Shutterstock" src="http://www.rsc.org/chemistryworld/sites/default/files/upload/biomass-power-plant_shutterstock_58957285_300.jpg" alt="" />Although some of the waste ash produced from the combustion of biomass is currently used in construction, most of it ends up in landfill. Therefore, extracting alkali silicates, which can be used in cement, detergents, catalysts and catalyst supports, is one way of reusing the potentially huge quantities of ash due to be produced in the future.</p>
<p>The team, led by <a href="http://www.york.ac.uk/chemistry/staff/academic/h-n/macquarrie/">Duncan Maquarrie</a> at the University of York, developed an efficient route for extracting the silicates by forming alkali silicate solutions. The silicate solutions were converted into the porous silica, MCM-41, a useful catalyst and molecular sieve.</p>
<p>Read what Duncan Macquarrie has to say about the research in <a href="http://www.rsc.org/chemistryworld/2013/04/biomass-ash-waste-mesoporous-silica"><strong>Chemistry World</strong></a>.</p>
<p>Read the original research published in <em>Green Chemistry</em>:</p>
<p><strong><span style="text-decoration: underline"><a href="http://xlink.rsc.org/?doi=10.1039/C3GC40324F">Alkali silicates and structured mesoporous silicas from biomass power station wastes: the emergence of bio-MCMs</a></span></strong>, J. R. Dodson,  E. C. Cooper,  A. J. Hunt,  A. Matharu,  J. Cole,  A. Minihan,  J. H. Clark and D. J. Macquarrie, <em>Green Chem.</em>, 2013, <strong>DOI: 10.1039/C3GC40324F</strong></p>
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		<title>Top 10 most accessed articles in January</title>
		<link>http://blogs.rsc.org/gc/2013/04/11/top-10-most-accessed-articles-in-january/</link>
		<comments>http://blogs.rsc.org/gc/2013/04/11/top-10-most-accessed-articles-in-january/#comments</comments>
		<pubDate>Thu, 11 Apr 2013 13:53:35 +0000</pubDate>
		<dc:creator>Bethany Johnson</dc:creator>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2704</guid>
		<description><![CDATA[For Green Chemistry, the top 10 most accessed articles in January were as follows:
Selective oxidation of alcohols and aldehydes over supported metal nanoparticles
Sara E. Davis, Matthew S. Ide and Robert J. Davis
Green Chem., 2013, 15, 17-45
DOI: 10.1039/C2GC36441G, Critical Review
Food waste biomass: a resource for high-value chemicals
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly [...]]]></description>
			<content:encoded><![CDATA[<p>For <strong><em><a href="http://pubs.rsc.org/en/journals/journalissues/gc" target="_blank">Green Chemistry</a></em></strong>, the top 10 most accessed articles in January were as follows:</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36441g" target="_blank">Selective oxidation of alcohols and aldehydes over supported metal nanoparticles</a><br />
Sara E. Davis, Matthew S. Ide and Robert J. Davis<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 17-45<br />
<strong>DOI</strong>: 10.1039/C2GC36441G, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36978h" target="_blank">Food waste biomass: a resource for high-value chemicals</a><br />
Lucie A. Pfaltzgraff, Mario De bruyn, Emma C. Cooper, Vitaly Budarin and James H. Clark<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 307-314<br />
<strong>DOI</strong>: 10.1039/C2GC36978H, Perspective</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36683e" target="_blank">A simple metal-free catalytic sulfoxidation under visible light and air</a><br />
Xiangyong Gu, Xiang Li, Yahong Chai, Qi Yang, Pixu Li and Yingming Yao<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 357-361<br />
<strong>DOI</strong>: 10.1039/C2GC36683E, Communication</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36364j" target="_blank">Deconstruction of lignocellulosic biomass with ionic liquids</a><br />
Agnieszka Brandt, John Gräsvik, Jason P. Hallett and Tom Welton<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 550-583<br />
<strong>DOI</strong>: 10.1039/C2GC36364J, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36900a" target="_blank">Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N,N-dimethylformamide</a><br />
Donna S. MacMillan, Jane Murray, Helen F. Sneddon, Craig Jamieson and Allan J. B. Watson<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 596-600<br />
<strong>DOI</strong>: 10.1039/C2GC36900A, Communication</p>
<p><a href="http://dx.doi.org/10.1039/c004654j" target="_blank">Catalytic conversion of biomass to biofuels</a><br />
David Martin Alonso, Jesse Q. Bond and James A. Dumesic<br />
<strong><em>Green Chem.,</em></strong> 2010, <strong>12</strong>, 1493-1513<br />
<strong>DOI</strong>: 10.1039/C004654J, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc35055f" target="_blank">Designing endocrine disruption out of the next generation of chemicals</a><br />
T. T. Schug, R. Abagyan, B. Blumberg, T. J. Collins, D. Crews, P. L. DeFur, S. M. Dickerson, T. M. Edwards, A. C. Gore, L. J. Guillette, T. Hayes, J. J. Heindel, A. Moores, H. B. Patisaul, T. L. Tal, K. A. Thayer, L. N. Vandenberg, J. C. Warner, C. S. Watson, F. S. vom Saal, R. T. Zoeller, K. P. O&#8217;Brien and J. P. Myers<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 181-198<br />
<strong>DOI</strong>: 10.1039/C2GC35055F, Paper</p>
<p><a href="http://dx.doi.org/10.1039/c3gc37065h" target="_blank">Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass</a><br />
David Martin Alonso, Stephanie G. Wettstein and James A. Dumesic<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 584-595<br />
<strong>DOI</strong>: 10.1039/C3GC37065H, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36534k" target="_blank">Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond</a><br />
Rocío García-Álvarez, Pascale Crochet and Victorio Cadierno<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 46-66<br />
<strong>DOI</strong>: 10.1039/C2GC36534K, Tutorial Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc36619c" target="_blank">Cyclometalated iridium complexes for transfer hydrogenation of carbonyl groups in water</a><br />
Yawen Wei, Dong Xue, Qian Lei, Chao Wang and Jianliang Xiao<br />
<strong><em>Green Chem.,</em></strong> 2013, <strong>15</strong>, 629-634<br />
<strong>DOI</strong>: 10.1039/C2GC36619C, Communication</p>
<p>Take a look at the articles, then let us know your thoughts and comments below.</p>
<p>Interested in submitting your own work to <strong><em><a href="http://www.rsc.org/Publishing/Journals/guidelines/AuthorGuidelines/JournalPolicy/Journals/GC.asp" target="_blank">Green Chemistry</a></em></strong>? You can <a href="http://mc.manuscriptcentral.com/gc" target="_blank">submit online</a> today, or <a href="mailto:green-rsc@rsc.org" target="_blank">email us</a> with your ideas and suggestions.</p>
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		<title>Recycling rare earth elements using ionic liquids</title>
		<link>http://blogs.rsc.org/gc/2013/04/05/recycling-rare-earth-elements-using-ionic-liquids/</link>
		<comments>http://blogs.rsc.org/gc/2013/04/05/recycling-rare-earth-elements-using-ionic-liquids/#comments</comments>
		<pubDate>Fri, 05 Apr 2013 09:24:27 +0000</pubDate>
		<dc:creator>Anna Simpson, Deputy Editor</dc:creator>
				<category><![CDATA[Hot Article]]></category>
		<category><![CDATA[News]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2699</guid>
		<description><![CDATA[Recycling old magnets, so that rare-earth metals can be re-used, could help to solve an urgent raw material supply problem in the electronics industry. Researchers from the University of Leuven, Belgium, have used ionic liquids to separate neodymium and samarium from transition metals like iron, manganese and cobalt – all elements that are used in [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignright" title="© Science Photo Library" src="http://www.rsc.org/chemistryworld/sites/default/files/upload/C0116156-Rare_earth_metals-SPL-resizedIF.jpg" alt="" />Recycling old magnets, so that rare-earth metals can be re-used, could help to solve <a href="http://www.rsc.org/chemistryworld/Issues/2011/January/CriticalThinking.asp">an urgent raw material supply problem</a> in the electronics industry. Researchers from the University of Leuven, Belgium, have <a href="http://pubs.rsc.org/en/content/articlelanding/2013/GC/C3GC40198G">used ionic liquids to separate neodymium and samarium</a> from transition metals like iron, manganese and cobalt – all elements that are used in the construction of permanent rare-earth magnets, which are found in electronic devices ranging from hard drives to air conditioners and wind turbines.</p>
<p>‘The process involves the liquid-liquid extraction of rare-earth metals from the other elements present in neodymium-iron-boron and samarium-cobalt magnets,’ explains <a href="http://www.kuleuven.be/wieiswie/en/person/u0007851">Koen Binnemans</a> who leads the group developing the process. ‘These other elements – including iron, cobalt, manganese, copper and zinc – are extracted into the ionic-liquid phase, while the rare-earth metals are left behind in the aqueous phase,’ he says, adding that the ionic liquid itself – trihexyl(tetradecyl)phosphonium chloride – can also be re-used, after the transition metals have been stripped out.</p>
<p>In traditional liquid-liquid extractions of metal ions, an aqueous phase containing the metal salt is mixed with an organic phase containing an extraction agent. Simple though they are, these processes use organic phases comprising flammable and volatile solvents, like toluene, kerosene or diethyl ether. Ionic liquids are far more environmentally friendly, having very low vapour pressure and non-flammability.</p>
<p>Read the <a href="http://www.rsc.org/chemistryworld/2013/03/recycling-rare-earth-neodymium-and-samarium-ionic-liquids">full article</a> in <em><strong>Chemistry World</strong></em></p>
<p>Read the original journal article in <em>Green Chemistry</em>:</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3GC40198G">Removal of transition metals from rare earths by solvent extraction with an undiluted phosphonium ionic liquid: separations relevant to rare-earth magnet recycling<br />
</a>Tom Vander Hoogerstraete,  Sil Wellens,  Katrien Verachtert and Koen Binnemans<br />
<em>Green Chem</em>., 2013,<strong>15</strong>, 919-927</p>
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		<title>Green Chemistry Issue 4 now online</title>
		<link>http://blogs.rsc.org/gc/2013/03/27/green-chemistry-issue-4-now-online-2/</link>
		<comments>http://blogs.rsc.org/gc/2013/03/27/green-chemistry-issue-4-now-online-2/#comments</comments>
		<pubDate>Wed, 27 Mar 2013 14:47:41 +0000</pubDate>
		<dc:creator>Anna Simpson, Deputy Editor</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2691</guid>
		<description><![CDATA[Green Chemistry issue 4 is now online and you can read it here.
The cover features work by François Jérôme and co-workers from France.  Their Paper, ‘Pretreatment of microcrystalline cellulose by ultrasounds: effect of particle size in the heterogeneously-catalyzed hydrolysis of cellulose to glucose’ demonstrates that activity of a sulfonated carbon in the heterogeneously-catalyzed hydrolysis of [...]]]></description>
			<content:encoded><![CDATA[<p><em>Green Chemistry </em>issue 4 is now online and you can read it <strong><a href="http://pubs.rsc.org/en/journals/journalissues/gc#!issueid=gc015004&amp;type=current&amp;issnprint=1463-9262">here</a></strong>.</p>
<p><a href="http://blogs.rsc.org/gc/files/2013/03/GC015004_ofc_800.jpg"><img class="size-medium wp-image-2692 alignleft" title="GC015004_ofc_800" src="http://blogs.rsc.org/gc/files/2013/03/GC015004_ofc_800-229x300.jpg" alt="Issue 4 front cover" width="137" height="180" /></a>The cover features work by François Jérôme and co-workers from France.  Their Paper, <a href="http://xlink.rsc.org/?doi=10.1039/C3GC36643J">‘Pretreatment of microcrystalline cellulose by ultrasounds: effect of particle size in the heterogeneously-catalyzed hydrolysis of cellulose to glucose’</a> demonstrates that activity of a sulfonated carbon in the heterogeneously-catalyzed hydrolysis of cellulose was greatly improved by assistance of ultrasound. The paper demonstrates that the sonication method was as effective as conventional pre-treatments such as ball-milling or ionic liquids.</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C3GC36643J" target="_blank">Pretreatment of microcrystalline cellulose by ultrasounds: effect of particle size in the heterogeneously-catalyzed hydrolysis of cellulose to glucose</a></strong><br />
Qinghua Zhang, Maud Benoit, Karine De Oliveira Vigier, Joël Barrault, Gwenaëlle Jégou, Michel Philippe and François Jérôme, <em>Green Chem</em>., 2013, <strong>15</strong>, 963-969</p>
<p><a href="http://blogs.rsc.org/gc/files/2013/03/GC015004_ifc_800.jpg"><img class="size-medium wp-image-2693 alignright" title="GC015004_ifc_800" src="http://blogs.rsc.org/gc/files/2013/03/GC015004_ifc_800-229x300.jpg" alt="Issue 4 inside cover" width="137" height="180" /></a></p>
<p>The inside front cover highlights a review article entitled <a href="http://xlink.rsc.org/?doi=10.1039/C3GC36994C" target="_blank">‘Green chemistry and the ocean-based biorefinery’ </a>by Fran Kerton and co-workers at the Memorial University of Newfoundland in Canada.  This review highlights that competition for land use could be minimized if marine sourced feedstocks were used for chemicals and materials production rather than crops grown on fertile land. It focuses on achievements and potential opportunities surrounding the use of algae and waste from shellfish and finfish processing.</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C3GC36994C" target="_blank">Green chemistry and the ocean-based biorefinery</a></strong><br />
Francesca M. Kerton, Yi Liu, Khaled W. Omari and Kelly Hawboldt, <em>Green Chem</em>., 2013, <strong>15</strong>, 860-871</p>
<p><strong><span style="color: #993300">These articles are free to access for 6 weeks!</span></strong></p>
<p><strong>Keep up-to-date with the latest content in <em>Green Chemistry</em> by </strong><a href="http://www.rsc.org/Publishing/Journals/forms/V5profile.asp" target="_blank"><strong>registering</strong></a><strong> for our free table of contents alerts.</strong></p>
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		<title>&#8216;Super solvents&#8217; shortlisted for most important British innovation of the 21st Century</title>
		<link>http://blogs.rsc.org/gc/2013/03/20/super-solvents-shortlisted-for-most-important-british-innovation-of-the-21st-century/</link>
		<comments>http://blogs.rsc.org/gc/2013/03/20/super-solvents-shortlisted-for-most-important-british-innovation-of-the-21st-century/#comments</comments>
		<pubDate>Wed, 20 Mar 2013 15:29:10 +0000</pubDate>
		<dc:creator>Mary Badcock, Deputy Editor</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2682</guid>
		<description><![CDATA[Work by scientists from Queen’s University Belfast on ionic liquid chemistry is in the running to be named the most important British innovation of the 21st Century. 
The work of staff in the Queen&#8217;s University Ionic Liquid Laboratories (QUILL) Research Centre is up against 11 other innovations from across the United Kingdom battling it out in a [...]]]></description>
			<content:encoded><![CDATA[<p><img class="alignright" title="(c) Shutterstock" src="http://blogs.rsc.org/gc/files/2012/07/1.jpg" alt="" width="250" height="247" />Work by scientists from Queen’s University Belfast on <strong><span style="color: #008080">ionic liquid chemistry</span></strong> is in the running to be named the most important British innovation of the 21<sup>st</sup> Century. </p>
<p>The work of staff in the Queen&#8217;s University Ionic Liquid Laboratories (QUILL) Research Centre is up against 11 other innovations from across the United Kingdom battling it out in a public vote to find the one that will have the greatest impact in the coming century. The vote is part of the Science Museum’s Initiative on Great British past and future Innovations. </p>
<p>Ionic liquids are salts which can remain liquid at room temperature and do not form vapours, and so can be used as non-polluting alternatives to conventional solvents.  At QUILL, a team of nearly 100 scientists are exploring the potential of these green solvents and Fortune 100 energy giant Petronas is already using the technology in its plants.  The mercury removal unit, using 15 tons of supported ionic liquid, was developed by a team led by Professor Ken Seddon, Co-Director of QUILL at Queen’s, and Dr John Holbrey also from QUILL, who were listed last year as the number one and two chemists in the UK based on citations of their work.Professor Ken Seddon said: “Being shortlisted for the most important British innovation of the 21<sup>st</sup> century is recognition of the high calibre of research being undertaken at QUILL and throughout the University.  We would encourage people to take a moment to vote for our research as its application will eventually have a bearing on most of our lives.”</p>
<p>Other notable British innovations in the hunt for the prize are Quantum Dots, Graphene, Raspberry Pi and the discovery of the Higgs-Boson &#8211; <strong>you can vote for your favourite </strong><a href="http://www.topbritishinnovations.org/FutureInnovations.aspx" target="_blank"><strong>here</strong></a><strong>.</strong>  <strong><span style="color: #008080">Update Monday 25th March &#8211; Ionic Liquid Chemistry was voted the recent innovation that is most likely to shape the coming century.</span></strong></p>
<p><strong></strong><span style="color: #000000">Why not take a look at a collection of high quality research in this area from across RSC Journals &#8211; <a href="http://blogs.rsc.org/gc/2012/07/16/incredible-ionic-liquids-an-article-collection/" target="_blank"><strong>Increadible ionic liquids: an article collection</strong></a>.</span></p>
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		<title>Top 10 most accessed articles in 2012</title>
		<link>http://blogs.rsc.org/gc/2013/03/15/top-10-most-accessed-articles-in-2012/</link>
		<comments>http://blogs.rsc.org/gc/2013/03/15/top-10-most-accessed-articles-in-2012/#comments</comments>
		<pubDate>Fri, 15 Mar 2013 10:38:52 +0000</pubDate>
		<dc:creator>Bethany Johnson</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Green]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/gc/?p=2676</guid>
		<description><![CDATA[Do you want to know what your colleagues were reading during 2012? The following articles in Green Chemistry were the most accessed over the course of the year:
Multicomponent reactions in unconventional solvents: state of the art
Yanlong Gu
Green Chem., 2012,14, 2091-2128
DOI: 10.1039/C2GC35635J, Critical Review
Characterization and comparison of hydrophilic and hydrophobic room temperature ionic liquids incorporating the imidazolium [...]]]></description>
			<content:encoded><![CDATA[<p>Do you want to know what your colleagues were reading during 2012? The following articles in <em><a href="http://pubs.rsc.org/en/journals/journalissues/gc">Green Chemistry</a></em> were the most accessed over the course of the year:</p>
<p><a href="http://dx.doi.org/10.1039/c2gc35635j">Multicomponent reactions in unconventional solvents: state of the art</a><br />
Yanlong Gu<br />
<em><strong>Green Chem.</strong></em>, 2012,<strong>14</strong>, 2091-2128<br />
<strong>DOI: </strong>10.1039/C2GC35635J, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/b103275p">Characterization and comparison of hydrophilic and hydrophobic room temperature ionic liquids incorporating the imidazolium cation</a><br />
Jonathan G. Huddleston, Ann E. Visser, W. Matthew Reichert, Heather D. Willauer, Grant A. Broker and Robin D. Rogers<br />
<em><strong>Green Chem.</strong></em>, 2001,<strong>3</strong>, 156-164<br />
<strong>DOI: </strong>10.1039/B103275P, Paper</p>
<p><a href="http://dx.doi.org/10.1039/c004654j">Catalytic conversion of biomass to biofuels</a><br />
David Martin Alonso, Jesse Q. Bond and James A. Dumesic<br />
<em><strong>Green Chem.</strong></em>, 2010,<strong>12</strong>, 1493-1513<br />
<strong>DOI: </strong>10.1039/C004654J, Critical Review</p>
<p><a href="c2gc16344f">Transition metal based catalysts in the aerobic oxidation of alcohols</a><br />
Camilla Parmeggiani and Francesca Cardona<br />
<em><strong>Green Chem.</strong></em>, 2012,<strong>14</strong>, 547-564<br />
<strong>DOI: </strong>10.1039/C2GC16344F, Tutorial Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc35160a">Evolution of asymmetric organocatalysis: multi- and retrocatalysis</a><br />
Raffael C. Wende and Peter R. Schreiner<br />
<em><strong>Green Chem.</strong></em>, 2012,<strong>14</strong>, 1821-1849<br />
<strong>DOI: </strong>10.1039/C2GC35160A, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c1gc15386b">Green synthesis of metal nanoparticles using plants</a><br />
Siavash Iravani<br />
<em><strong>Green Chem.</strong></em>, 2011,<strong>13</strong>, 2638-2650<br />
<strong>DOI: </strong>10.1039/C1GC15386B, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/b922014c">Technology development for the production of biobased products from biorefinery carbohydrates—the US Department of Energy&#8217;s “Top 10” revisited</a><br />
Joseph J. Bozell and Gene R. Petersen<br />
<em><strong>Green Chem.</strong></em>, 2010,<strong>12</strong>, 539-554<br />
<strong>DOI: </strong>10.1039/B922014C, Critical Review</p>
<p><a href="http://dx.doi.org/10.1039/c1gc16022b">Continuous flow reactors: a perspective</a><br />
Charlotte Wiles and Paul Watts<br />
<em><strong>Green Chem.</strong></em>, 2012,<strong>14</strong>, 38-54<br />
<strong>DOI: </strong>10.1039/C1GC16022B, Tutorial Review</p>
<p><a href="http://dx.doi.org/10.1039/c2gc35203f">Catalytic conversion of biomass using solvents derived from lignin</a><br />
Pooya Azadi, Ronald Carrasquillo-Flores, Yomaira J. Pagán-Torres, Elif I. Gürbüz, Ramin Farnood and James A. Dumesic<br />
<em><strong>Green Chem.</strong></em>, 2012,<strong>14</strong>, 1573-1576<br />
<strong>DOI: </strong>10.1039/C2GC35203F, Communication</p>
<p><a href="http://dx.doi.org/10.1039/c0gc00401d">5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications</a><br />
Andreia A. Rosatella, Svilen P. Simeonov, Raquel F. M. Frade and Carlos A. M. Afonso<br />
<em><strong>Green Chem.</strong></em>, 2011,<strong>13</strong>, 754-793<br />
<strong>DOI: </strong>10.1039/C0GC00401D, Critical Review</p>
<p>Take a look at the articles and then post your thoughts and comments below.</p>
<p>Interested in submitting your own work to <em>Green Chemistry</em>? <a href="http://mc.manuscriptcentral.com/gc" target="_blank">Submit online</a> today, or <a href="mailto:green-rsc@rsc.org" target="_blank">email us</a> with your suggestions.</p>
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