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		<title>Sustainability: Sustainable Approaches within the Chemical Sciences</title>
		<link>http://www.mdpi.com/journal/sustainability/special_issues/sustainable-chemistry/</link>
		<description>Dear Colleagues,

Sustainability and approaches that are along the line with the principles of green chemistry are already now in the focus of many chemists. Some important issues that need our attention are the minimization of (toxic) waste, the use of efficient catalytic chemical reactions, the sustainable utilization of renewable feedstocks, and many others. In addition, it is very important to include these concepts to the curriculum of our students in order to educate a future generation of chemists that will not repeat the mistakes made by their predecessors. 

Prof. Dr.  Michael A. R. Meier 
Guest Editor
Related Section in other Journals
Green Chemistry in IJMS

Related Special Issues in other Journals
Advances in Green Chemistry and Sustainable Chemistry in IJMS.

Submission
 
All manuscripts should be submitted to sustainability@mdpi.com with a copy to the Guest Editor. Manuscripts can be submitted until the deadline. Papers will be published continuously (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.
 
Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are refereed through a peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Sustainability is an international peer-reviewed Open Access monthly journal published by MDPI.
 
Please visit the Instructions for Authors page before submitting a manuscript. Article Processing Charges (APC) for publication in this Open Access journal are 300 CHF (Swiss Francs) per accepted Paper. English correction and/or formatting fees of 250 CHF (Swiss Francs) will be charged in certain cases for those articles accepted for publication that require extensive additional formatting and/or English corrections.</description>
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	<title>Sustainability, Vol. 1, Pages 1226-1239: New Challenge for Classics: Neutral Zinc Complexes Stabilised by 2,2’-Bipyridine and 1,10-Phenanthroline and Their Application in the Ring-Opening Polymerisation of Lactide</title>
	<link>http://www.mdpi.com/2071-1050/1/4/1226/</link>
	<description>The zinc acetato and triflato complexes of 2,2’-bipyridine and 1,10-phenanthroline were prepared and completely characterised. The whole series (including the already described dichlorido complexes and the ligands themselves) were screened for their catalytic activity in the solvent free ring-opening polymerisation of D,L-lactide. The acetato and triflato complexes were found to be active initiators and polylactides could be obtained in almost quantitative yields or with high molecular weights, up to 145,000 g/mol.</description>
	
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	<pubDate>Tue, 08 Dec 2009 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sustainability</prism:publicationName>
	<prism:publicationDate>2009-12-08</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1226</prism:startingPage>
		<prism:endingPage>1239</prism:endingPage>
		<prism:issn>2071-1050</prism:issn>
	
	<dc:title>New Challenge for Classics: Neutral Zinc Complexes Stabilised by 2,2’-Bipyridine and 1,10-Phenanthroline and Their Application in the Ring-Opening Polymerisation of Lactide</dc:title>
	<dc:date>2009-12-08</dc:date>
	<dc:identifier>doi: 10.3390/su1041226</dc:identifier>
		<dc:creator>Janna Börner</dc:creator>
		<dc:creator>Ulrich Flörke</dc:creator>
		<dc:creator>Artjom Döring</dc:creator>
		<dc:creator>Dirk Kuckling</dc:creator>
		<dc:creator>Matthew D. Jones</dc:creator>
		<dc:creator>Sonja Herres-Pawlis</dc:creator>
	
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	<title>Sustainability, Vol. 1, Pages 924-945: Chemically Modified Cyclodextrins: An Attractive Class of Supramolecular Hosts for the Development of Aqueous Biphasic Catalytic Processes</title>
	<link>http://www.mdpi.com/2071-1050/1/4/924/</link>
	<description>During these last years, cyclodextrins have contributed greatly to the development of catalytic processes in water. These cyclic oligosaccharides composed of 6(α), 7(β) or 8(γ) glucopyranose units improve the mass transfer in aqueous-organic two-phase systems and are useful compounds to design new catalysts. Thus, chemically modified cyclodextrins can be used to: (i) increase significantly the rate and selectivity of reactions catalyzed by water-soluble organometallic complexes, (ii) design new water-soluble ligands for aqueous organometallic catalysis, (iii) stabilize catalytically active noble metal nanoparticles in water and (iv) favour the dispersion and activation of the palladium on charcoal in water.</description>
	
	<guid>http://www.mdpi.com/2071-1050/1/4/924/</guid>
	<pubDate>Tue, 27 Oct 2009 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sustainability</prism:publicationName>
	<prism:publicationDate>2009-10-27</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>924</prism:startingPage>
		<prism:endingPage>945</prism:endingPage>
		<prism:issn>2071-1050</prism:issn>
	
	<dc:title>Chemically Modified Cyclodextrins: An Attractive Class of Supramolecular Hosts for the Development of Aqueous Biphasic Catalytic Processes</dc:title>
	<dc:date>2009-10-27</dc:date>
	<dc:identifier>doi: 10.3390/su1040924</dc:identifier>
		<dc:creator>Hervé Bricout</dc:creator>
		<dc:creator>Frédéric Hapiot</dc:creator>
		<dc:creator>Anne Ponchel</dc:creator>
		<dc:creator>Sébastien Tilloy</dc:creator>
		<dc:creator>Eric Monflier</dc:creator>
	
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