<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>34469</id>
    <completedYear/>
    <publishedYear>2015</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>3787</pageFirst>
    <pageLast>3791</pageLast>
    <pageNumber/>
    <edition/>
    <issue>12</issue>
    <volume>13</volume>
    <type>article</type>
    <publisherName>RSC</publisherName>
    <publisherPlace>Cambridge</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Gold-catalyzed allene cycloisomerization for pyrrole synthesis: towards highly fluorinated BODIPY dyes</title>
    <abstract language="eng">A novel synthetic strategy toward highly fluorinated BODIPY dyes with exceptional photostabilities relying on sustainable gold catalysis has been developed. A key to the tailored pyrrole precursors is the gold catalysis performed in ionic liquids as the reaction medium, allowing a facile recycling of the catalysts. The dyes prepared are well-matching with the spectral windows of popular rhodamine dyes and possess high brightness while showing a distinctly higher photostability than the rhodamines especially in aprotic solvents.</abstract>
    <parentTitle language="eng">Organic &amp; biomolecular chemistry</parentTitle>
    <identifier type="old">37602</identifier>
    <identifier type="doi">10.1039/c4ob02671c</identifier>
    <identifier type="issn">1477-0520</identifier>
    <identifier type="issn">1477-0539</identifier>
    <identifier type="urn">urn:nbn:de:kobv:b43-344692</identifier>
    <enrichment key="date_peer_review">12.10.2015</enrichment>
    <licence>Creative Commons - Namensnennung 3.0</licence>
    <author>L. Lempke</author>
    <author>Tobias Fischer</author>
    <author>Jérémy Bell</author>
    <author>Werner Kraus</author>
    <author>Knut Rurack</author>
    <author>N. Krause</author>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Gold-Katalyse</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>BODIPY-Farbstoffe</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Photostabilität</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Fluor-Substitution</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Fluoreszenz</value>
    </subject>
    <collection role="ddc" number="543">Analytische Chemie</collection>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei für die Öffentlichkeit verfügbar ("Open Access")</collection>
    <collection role="unnumberedseries" number="">Wissenschaftliche Artikel der BAM</collection>
    <thesisPublisher>Bundesanstalt für Materialforschung und -prüfung (BAM)</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-bam/files/34469/Gold-catalyzed Allene Cycloisomerization for Pyrrole Synthesis  Towards Highly Fluorinated BODIPY Dyes_Lempke.pdf</file>
  </doc>
</export-example>
