<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns="http://purl.org/rss/1.0/">
<channel rdf:about="http://www.nature.com/nchem/current_issue/rss">
<title>Nature Chemistry</title>
<description>Nature Chemistry is a unique forum for chemists of all disciplines. Every month Nature Chemistry publishes original top-quality research, plus a compelling mix of news and reviews, in print and online.</description>
<link>http://www.nature.com/nchem/current_issue/</link>
<dc:publisher>Nature Publishing Group</dc:publisher>
<dc:language>en</dc:language>
<dc:rights>&#169; 2008 Nature Publishing Group</dc:rights>
<prism:publicationName>Nature Chemistry</prism:publicationName>
<prism:issn>1745-2473</prism:issn>
<prism:eIssn>1745-2481</prism:eIssn>
<prism:copyright>&#169; 2008 Nature Publishing Group</prism:copyright>
<prism:rightsAgent>permissions@nature.com</prism:rightsAgent>
<image rdf:resource="http://www.nature.com/includes/rj_globnavimages/nchem_logo.gif"/>
<items>
<rdf:Seq>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nchem.88"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nchem.89"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/nchem.90"/>
</rdf:Seq>
</items>
</channel>
<image rdf:about="http://www.nature.com/includes/rj_globnavimages/nchem_logo.gif">
<title>Nature Chemistry</title>
<url>http://www.nature.com/includes/rj_globnavimages/nchem_logo.gif</url>
<link>http://www.nature.com/nchem/</link>
</image>
<item rdf:about="http://dx.doi.org/10.1038/nchem.88">
<title>Graphene synthesis: Chemical peel</title>
<link>http://dx.doi.org/10.1038/nchem.88</link>
<description>Large graphene sheets can be prepared by reduction of graphite oxide in pure hydrazine</description>
<content:encoded><![CDATA[

<p>
<b>Graphene synthesis: Chemical peel</b>
</p>
<p>Nature Chemistry(2008). <a href="http://dx.doi.org/10.1038/nchem.88">doi:10.1038/nchem.88</a>
</p>
<p>Author: Anne Pichon</p>
<p>Large graphene sheets can be prepared by reduction of graphite oxide in pure hydrazine</p>
]]></content:encoded>
<dc:title>Graphene synthesis: Chemical peel</dc:title>
<dc:creator>Anne Pichon</dc:creator>
<dc:identifier>doi:10.1038/nchem.88</dc:identifier>
<dc:source>Nature Chemistry(2008)</dc:source>
<dc:date>2008-11-14</dc:date>
<prism:publicationName>Nature Chemistry</prism:publicationName>
<prism:publicationDate>2008-11-14</prism:publicationDate>
<prism:section>Research Highlights</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nchem.89">
<title>Microfluidics: Introducing the chemistrode</title>
<link>http://dx.doi.org/10.1038/nchem.89</link>
<description>A microfluidic 'chemistrode' device has been developed for stimulating, recording and analysing molecular signals</description>
<content:encoded><![CDATA[

<p>
<b>Microfluidics: Introducing the chemistrode</b>
</p>
<p>Nature Chemistry(2008). <a href="http://dx.doi.org/10.1038/nchem.89">doi:10.1038/nchem.89</a>
</p>
<p>Author: Gavin Armstrong</p>
<p>A microfluidic 'chemistrode' device has been developed for stimulating, recording and analysing molecular signals</p>
]]></content:encoded>
<dc:title>Microfluidics: Introducing the chemistrode</dc:title>
<dc:creator>Gavin Armstrong</dc:creator>
<dc:identifier>doi:10.1038/nchem.89</dc:identifier>
<dc:source>Nature Chemistry(2008)</dc:source>
<dc:date>2008-11-14</dc:date>
<prism:publicationName>Nature Chemistry</prism:publicationName>
<prism:publicationDate>2008-11-14</prism:publicationDate>
<prism:section>Research Highlights</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nchem.90">
<title>Hypervalent compounds: Sulfur, so good</title>
<link>http://dx.doi.org/10.1038/nchem.90</link>
<description>A sulfur-substituted organosulfurane &#8212; with a four-coordinate 'hypervalent' sulfur atom &#8212; is shown to be reversibly reducible</description>
<content:encoded><![CDATA[

<p>
<b>Hypervalent compounds: Sulfur, so good</b>
</p>
<p>Nature Chemistry(2008). <a href="http://dx.doi.org/10.1038/nchem.90">doi:10.1038/nchem.90</a>
</p>
<p>Author: Neil Withers</p>
<p>A sulfur-substituted organosulfurane &#8212; with a four-coordinate 'hypervalent' sulfur atom &#8212; is shown to be reversibly reducible</p>
]]></content:encoded>
<dc:title>Hypervalent compounds: Sulfur, so good</dc:title>
<dc:creator>Neil Withers</dc:creator>
<dc:identifier>doi:10.1038/nchem.90</dc:identifier>
<dc:source>Nature Chemistry(2008)</dc:source>
<dc:date>2008-11-14</dc:date>
<prism:publicationName>Nature Chemistry</prism:publicationName>
<prism:publicationDate>2008-11-14</prism:publicationDate>
<prism:section>Research Highlights</prism:section>
</item>
</rdf:RDF>
