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<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc90031e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1617</fpage>
<lpage>1617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc90031e">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inside front cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc90032c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1618</fpage>
<lpage>1618</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc90032c">Abstract</self-uri>
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<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Contents list</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc90033a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1619</fpage>
<lpage>1631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc90033a">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dendrimer-encapsulated nanoparticles: New synthetic and characterization methods and catalytic applications</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00256b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Myers</surname>
<given-names>V. Sue</given-names></name>
<name><surname>Weir</surname>
<given-names>Michael G.</given-names></name>
<name><surname>Carino</surname>
<given-names>Emily V.</given-names></name>
<name><surname>Yancey</surname>
<given-names>David F.</given-names></name>
<name><surname>Pande</surname>
<given-names>Surojit</given-names></name>
<name><surname>Crooks</surname>
<given-names>Richard M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1632</fpage>
<lpage>1646</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00256b">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Energy transfer at metal surfaces: the need to go beyond the electronic friction picture</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00181g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartels</surname>
<given-names>Christof</given-names></name>
<name><surname>Cooper</surname>
<given-names>Russell</given-names></name>
<name><surname>Auerbach</surname>
<given-names>Daniel J.</given-names></name>
<name><surname>Wodtke</surname>
<given-names>Alec M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1647</fpage>
<lpage>1655</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00181g">Abstract</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular docking for virtual screening of natural product databases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00152c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ma</surname>
<given-names>Dik-Lung</given-names></name>
<name><surname>Chan</surname>
<given-names>Daniel Shiu-Hin</given-names></name>
<name><surname>Leung</surname>
<given-names>Chung-Hang</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1656</fpage>
<lpage>1665</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00152c">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Methods for converting cysteine to dehydroalanine on peptides and proteins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00185j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chalker</surname>
<given-names>Justin M.</given-names></name>
<name><surname>Gunnoo</surname>
<given-names>Smita B.</given-names></name>
<name><surname>Boutureira</surname>
<given-names>Omar</given-names></name>
<name><surname>Gerstberger</surname>
<given-names>Stefanie C.</given-names></name>
<name><surname>Fernández-González</surname>
<given-names>Marta</given-names></name>
<name><surname>Bernardes</surname>
<given-names>Gonçalo J. L.</given-names></name>
<name><surname>Griffin</surname>
<given-names>Laura</given-names></name>
<name><surname>Hailu</surname>
<given-names>Hanna</given-names></name>
<name><surname>Schofield</surname>
<given-names>Christopher J.</given-names></name>
<name><surname>Davis</surname>
<given-names>Benjamin G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1666</fpage>
<lpage>1676</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00185j">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Powering reductive charge shift reactions—linking fullerenes of different electron acceptor strength to secure an energy gradient</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00331c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Villegas</surname>
<given-names>Carmen</given-names></name>
<name><surname>Delgado</surname>
<given-names>Juan Luis</given-names></name>
<name><surname>Bouit</surname>
<given-names>Pierre-Antoine</given-names></name>
<name><surname>Grimm</surname>
<given-names>Bruno</given-names></name>
<name><surname>Seitz</surname>
<given-names>Wolfgang</given-names></name>
<name><surname>Martín</surname>
<given-names>Nazario</given-names></name>
<name><surname>Guldi</surname>
<given-names>Dirk M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1677</fpage>
<lpage>1681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00331c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00331c">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Single-walled carbon nanotubes shell decorating porous silicate materials: A general platform for studying the interaction of carbon nanotubes with photoactive molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00323b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Saha</surname>
<given-names>Avishek</given-names></name>
<name><surname>Ghosh</surname>
<given-names>Saunab</given-names></name>
<name><surname>Behabtu</surname>
<given-names>Natnael</given-names></name>
<name><surname>Pasquali</surname>
<given-names>Matteo</given-names></name>
<name><surname>Martí</surname>
<given-names>Angel A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1682</fpage>
<lpage>1687</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00323b">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Influence of structure on exchange strength and relaxation barrier in a series of Fe&lt;sup&gt;II&lt;/sup&gt;Re&lt;sup&gt;IV&lt;/sup&gt;(CN)&lt;sub&gt;2&lt;/sub&gt; single-chain magnets</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00220a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feng</surname>
<given-names>Xiaowen</given-names></name>
<name><surname>Harris</surname>
<given-names>T. David</given-names></name>
<name><surname>Long</surname>
<given-names>Jeffrey R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1688</fpage>
<lpage>1694</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00220a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00220a">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Insight into the construction of metal–organic polyhedra: metal–organic cubes as a case study</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00269d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alkordi</surname>
<given-names>Mohamed H.</given-names></name>
<name><surname>Belof</surname>
<given-names>Jonathan L.</given-names></name>
<name><surname>Rivera</surname>
<given-names>Edwin</given-names></name>
<name><surname>Wojtas</surname>
<given-names>Lukasz</given-names></name>
<name><surname>Eddaoudi</surname>
<given-names>Mohamed</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1695</fpage>
<lpage>1705</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00269d">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of flinderoles B and C by a gold-catalyzed allene hydroarylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00290b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zeldin</surname>
<given-names>Rachel M.</given-names></name>
<name><surname>Toste</surname>
<given-names>F. Dean</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1706</fpage>
<lpage>1709</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00290b">Abstract</self-uri>
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<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A practical, convergent route to the key precursor to the tetracycline antibiotics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00303h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kummer</surname>
<given-names>David A.</given-names></name>
<name><surname>Li</surname>
<given-names>Derun</given-names></name>
<name><surname>Dion</surname>
<given-names>Amelie</given-names></name>
<name><surname>Myers</surname>
<given-names>Andrew G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1710</fpage>
<lpage>1718</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00303h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00303h">HTML</self-uri>
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<article>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dative boron–nitrogen bonds in structural supramolecular chemistry: multicomponent assembly of prismatic organic cages</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00320h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Icli</surname>
<given-names>Burcak</given-names></name>
<name><surname>Sheepwash</surname>
<given-names>Erin</given-names></name>
<name><surname>Riis-Johannessen</surname>
<given-names>Thomas</given-names></name>
<name><surname>Schenk</surname>
<given-names>Kurt</given-names></name>
<name><surname>Filinchuk</surname>
<given-names>Yaroslav</given-names></name>
<name><surname>Scopelliti</surname>
<given-names>Rosario</given-names></name>
<name><surname>Severin</surname>
<given-names>Kay</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1719</fpage>
<lpage>1721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00320h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00320h">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Operational calixarene-based fluorescent sensing systems for choline and acetylcholine and their application to enzymatic reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00231g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Guo</surname>
<given-names>Dong-Sheng</given-names></name>
<name><surname>Uzunova</surname>
<given-names>Vanya D.</given-names></name>
<name><surname>Su</surname>
<given-names>Xin</given-names></name>
<name><surname>Liu</surname>
<given-names>Yu</given-names></name>
<name><surname>Nau</surname>
<given-names>Werner M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1722</fpage>
<lpage>1734</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00231g">Abstract</self-uri>
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<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tunable, shape-shifting capsule for dicarboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00292a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wang</surname>
<given-names>Qi-Qiang</given-names></name>
<name><surname>Day</surname>
<given-names>Victor W.</given-names></name>
<name><surname>Bowman-James</surname>
<given-names>Kristin</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1735</fpage>
<lpage>1738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00292a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00292a">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;In vitro&lt;/i&gt; gene expression and enzyme catalysis in bio-inorganic protocells</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00183c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Li</surname>
<given-names>Mei</given-names></name>
<name><surname>Green</surname>
<given-names>David C.</given-names></name>
<name><surname>Anderson</surname>
<given-names>J. L. Ross</given-names></name>
<name><surname>Binks</surname>
<given-names>Bernard P.</given-names></name>
<name><surname>Mann</surname>
<given-names>Stephen</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1739</fpage>
<lpage>1745</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00183c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00183c">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopy and ionization thresholds of π-isoelectronic 1-phenylallyl and benzylallenyl resonance stabilized radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00246e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sebree</surname>
<given-names>Joshua A.</given-names></name>
<name><surname>Kidwell</surname>
<given-names>Nathanael M.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>Evan G.</given-names></name>
<name><surname>Zgierski</surname>
<given-names>Marek Z.</given-names></name>
<name><surname>Zwier</surname>
<given-names>Timothy S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1746</fpage>
<lpage>1754</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00246e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00246e">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The spectroscopy and thermochemistry of phenylallyl radical chromophores</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00247c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Troy</surname>
<given-names>Tyler P.</given-names></name>
<name><surname>Chalyavi</surname>
<given-names>Nahid</given-names></name>
<name><surname>Menon</surname>
<given-names>Ambili S.</given-names></name>
<name><surname>O'Connor</surname>
<given-names>Gerard D.</given-names></name>
<name><surname>Fückel</surname>
<given-names>Burkhard</given-names></name>
<name><surname>Nauta</surname>
<given-names>Klaas</given-names></name>
<name><surname>Radom</surname>
<given-names>Leo</given-names></name>
<name><surname>Schmidt</surname>
<given-names>Timothy W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1755</fpage>
<lpage>1765</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00247c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00247c">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nickel-catalyzed amination of aryl carbamates and sequential site-selective cross-couplings</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00230a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mesganaw</surname>
<given-names>Tehetena</given-names></name>
<name><surname>Silberstein</surname>
<given-names>Amanda L.</given-names></name>
<name><surname>Ramgren</surname>
<given-names>Stephen D.</given-names></name>
<name><surname>Nathel</surname>
<given-names>Noah F. Fine</given-names></name>
<name><surname>Hong</surname>
<given-names>Xin</given-names></name>
<name><surname>Liu</surname>
<given-names>Peng</given-names></name>
<name><surname>Garg</surname>
<given-names>Neil K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1766</fpage>
<lpage>1771</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00230a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00230a">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00194a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atienza</surname>
<given-names>Roxanne L.</given-names></name>
<name><surname>Roth</surname>
<given-names>Howard S.</given-names></name>
<name><surname>Scheidt</surname>
<given-names>Karl A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1772</fpage>
<lpage>1776</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00194a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00194a">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Band gap engineering in fluorescent conjugated microporous polymers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00329a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jiang</surname>
<given-names>Jia-Xing</given-names></name>
<name><surname>Trewin</surname>
<given-names>Abbie</given-names></name>
<name><surname>Adams</surname>
<given-names>Dave J.</given-names></name>
<name><surname>Cooper</surname>
<given-names>Andrew I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1777</fpage>
<lpage>1781</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00329a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00329a">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical control of interstitial iron leading to superconductivity in Fe&lt;sub&gt;1+&lt;i&gt;x&lt;/i&gt;&lt;/sub&gt;Te&lt;sub&gt;0.7&lt;/sub&gt;Se&lt;sub&gt;0.3&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00114k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rodriguez</surname>
<given-names>Efrain E.</given-names></name>
<name><surname>Stock</surname>
<given-names>Christopher</given-names></name>
<name><surname>Hsieh</surname>
<given-names>Ping-Yen</given-names></name>
<name><surname>Butch</surname>
<given-names>Nicholas P.</given-names></name>
<name><surname>Paglione</surname>
<given-names>Johnpierre</given-names></name>
<name><surname>Green</surname>
<given-names>Mark A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1782</fpage>
<lpage>1787</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00114k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00114k">HTML</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An anti-cancer trinuclear ruthenium(iii) complex with 2-thiosalicylate ligands attenuates Wnt-β-catenin signaling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00203a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>Sharon Lai-Fung</given-names></name>
<name><surname>Sun</surname>
<given-names>Raymond Wai-Yin</given-names></name>
<name><surname>Choi</surname>
<given-names>Mei-Yuk</given-names></name>
<name><surname>Zeng</surname>
<given-names>Yibo</given-names></name>
<name><surname>Shek</surname>
<given-names>Lam</given-names></name>
<name><surname>Chui</surname>
<given-names>Stephen Sin-Yin</given-names></name>
<name><surname>Che</surname>
<given-names>Chi-Ming</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1788</fpage>
<lpage>1792</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00203a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00203a">HTML</self-uri>
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</article>
<article>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
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<title-group>
<article-title>Distinct conformational preferences of prolinol and prolinol ether enamines in solution revealed by NMR</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00274k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schmid</surname>
<given-names>Markus B.</given-names></name>
<name><surname>Zeitler</surname>
<given-names>Kirsten</given-names></name>
<name><surname>Gschwind</surname>
<given-names>Ruth M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1793</fpage>
<lpage>1803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00274k">Abstract</self-uri>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
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<title-group>
<article-title>A transient kinetic study between signaling proteins: the case of the MEK–ERK interaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00268f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barbero</surname>
<given-names>Nadia</given-names></name>
<name><surname>Napione</surname>
<given-names>Lucia</given-names></name>
<name><surname>Visentin</surname>
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<name><surname>Viscardi</surname>
<given-names>Guido</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1804</fpage>
<lpage>1809</lpage>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
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<title-group>
<article-title>NMR as a probe of nanostructured domains in ionic liquids: Does domain segregation explain increased performance of free radical polymerisation?</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00207d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Puttick</surname>
<given-names>Simon</given-names></name>
<name><surname>Davis</surname>
<given-names>Adrienne L.</given-names></name>
<name><surname>Butler</surname>
<given-names>Kevin</given-names></name>
<name><surname>Lambert</surname>
<given-names>Lynette</given-names></name>
<name><surname>harfi</surname>
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<name><surname>Whittaker</surname>
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<name><surname>Thurecht</surname>
<given-names>Kristofer J.</given-names></name>
<name><surname>Licence</surname>
<given-names>Peter</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1810</fpage>
<lpage>1816</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00207d">Abstract</self-uri>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Surface enhanced Raman scattering of Ag or Au nanoparticle-decorated reduced graphene oxide for detection of aromatic molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00254f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lu</surname>
<given-names>Gang</given-names></name>
<name><surname>Li</surname>
<given-names>Hai</given-names></name>
<name><surname>Liusman</surname>
<given-names>Cipto</given-names></name>
<name><surname>Yin</surname>
<given-names>Zongyou</given-names></name>
<name><surname>Wu</surname>
<given-names>Shixin</given-names></name>
<name><surname>Zhang</surname>
<given-names>Hua</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1817</fpage>
<lpage>1821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00254f">Abstract</self-uri>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
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<title-group>
<article-title>Synthesis and characterization of a cyclic vinylpalladium(ii) complex: vinylpalladium species as the possible intermediate in the catalytic direct olefination reaction of enamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00262g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Xu</surname>
<given-names>Yun-He</given-names></name>
<name><surname>Chok</surname>
<given-names>Yew Keong</given-names></name>
<name><surname>Loh</surname>
<given-names>Teck-Peng</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1822</fpage>
<lpage>1825</lpage>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic semiconductor for artificial photosynthesis: water splitting into hydrogen by a bioinspired C&lt;sub&gt;3&lt;/sub&gt;N&lt;sub&gt;3&lt;/sub&gt;S&lt;sub&gt;3&lt;/sub&gt; polymer under visible light irradiation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00257k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zhang</surname>
<given-names>Zizhong</given-names></name>
<name><surname>Long</surname>
<given-names>Jinlin</given-names></name>
<name><surname>Yang</surname>
<given-names>Lifang</given-names></name>
<name><surname>Chen</surname>
<given-names>Wenkai</given-names></name>
<name><surname>Dai</surname>
<given-names>Wenxin</given-names></name>
<name><surname>Fu</surname>
<given-names>Xianzhi</given-names></name>
<name><surname>Wang</surname>
<given-names>Xuxu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1826</fpage>
<lpage>1830</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00257k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00257k">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photoinduced reactivity of Au–H intermediates in alcohol oxidation by gold nanoparticles supported on ceria</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00283j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maldotti</surname>
<given-names>Andrea</given-names></name>
<name><surname>Molinari</surname>
<given-names>Alessandra</given-names></name>
<name><surname>Juárez</surname>
<given-names>Raquel</given-names></name>
<name><surname>Garcia</surname>
<given-names>Hermenegildo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1831</fpage>
<lpage>1834</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00283j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00283j">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine/carbene cascade catalysis in the diastereo- and enantioselective synthesis of functionalized cyclopentanones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00175b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ozboya</surname>
<given-names>Kerem E.</given-names></name>
<name><surname>Rovis</surname>
<given-names>Tomislav</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1835</fpage>
<lpage>1838</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00175b">Abstract</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enantioselective bromination/semipinacol rearrangement for the synthesis of β-bromoketones containing an all-α-carbon quaternary center</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00295c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Li</surname>
<given-names>Hui</given-names></name>
<name><surname>Zhang</surname>
<given-names>Fu-Min</given-names></name>
<name><surname>Tu</surname>
<given-names>Yong-Qiang</given-names></name>
<name><surname>Zhang</surname>
<given-names>Qing-Wei</given-names></name>
<name><surname>Chen</surname>
<given-names>Zhi-Min</given-names></name>
<name><surname>Chen</surname>
<given-names>Zhi-Hua</given-names></name>
<name><surname>Li</surname>
<given-names>Jian</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1839</fpage>
<lpage>1841</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00295c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00295c">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular frustrated N/B lewis pairs by enamine hydroboration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00124h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schwendemann</surname>
<given-names>Sina</given-names></name>
<name><surname>Fröhlich</surname>
<given-names>Roland</given-names></name>
<name><surname>Kehr</surname>
<given-names>Gerald</given-names></name>
<name><surname>Erker</surname>
<given-names>Gerhard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1842</fpage>
<lpage>1849</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00124h">Abstract</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A new polymerisation route to conjugated polymers: regio- and stereoselective synthesis of linear and hyperbranched poly(arylene chlorovinylene)s by decarbonylative polyaddition of aroyl chlorides and alkynes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00300c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Liu</surname>
<given-names>Jianzhao</given-names></name>
<name><surname>Deng</surname>
<given-names>Chunmei</given-names></name>
<name><surname>Tseng</surname>
<given-names>Nai-Wen</given-names></name>
<name><surname>Chan</surname>
<given-names>Carrie Y. K.</given-names></name>
<name><surname>Yue</surname>
<given-names>Yanan</given-names></name>
<name><surname>Ng</surname>
<given-names>Jason C. Y.</given-names></name>
<name><surname>Lam</surname>
<given-names>Jacky W. Y.</given-names></name>
<name><surname>Wang</surname>
<given-names>Jian</given-names></name>
<name><surname>Hong</surname>
<given-names>Yuning</given-names></name>
<name><surname>Sung</surname>
<given-names>Herman H. Y.</given-names></name>
<name><surname>Williams</surname>
<given-names>Ian D.</given-names></name>
<name><surname>Tang</surname>
<given-names>Ben Zhong</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1850</fpage>
<lpage>1859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00300c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticleHtml/2011/SC/c1sc00300c">HTML</self-uri>
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<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>TiO&lt;sub&gt;2&lt;/sub&gt;-decorated graphenes as efficient photoswitches with high oxygen sensitivity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc00344e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wang</surname>
<given-names>Qing</given-names></name>
<name><surname>Guo</surname>
<given-names>Xuefeng</given-names></name>
<name><surname>Cai</surname>
<given-names>Lichao</given-names></name>
<name><surname>Cao</surname>
<given-names>Yang</given-names></name>
<name><surname>Gan</surname>
<given-names>Lin</given-names></name>
<name><surname>Liu</surname>
<given-names>Song</given-names></name>
<name><surname>Wang</surname>
<given-names>Zhenxing</given-names></name>
<name><surname>Zhang</surname>
<given-names>Hongtao</given-names></name>
<name><surname>Li</surname>
<given-names></given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1860</fpage>
<lpage>1864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc00344e">Abstract</self-uri>
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</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Back matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc90035h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1865</fpage>
<lpage>1866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc90035h">Abstract</self-uri>
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<article>
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<journal-meta>
<journal-title>Chemical Science</journal-title>
<issn>2041-6520</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Back cover</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/c1sc90034j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>2011</year></pub-date>
<volume>2</volume>
<issue>9</issue>
<fpage>1867</fpage>
<lpage>1868</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=c1sc90034j">Abstract</self-uri>
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