<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>12563</id>
    <completedYear/>
    <publishedYear>2006</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>2239</pageFirst>
    <pageLast>2241</pageLast>
    <pageNumber/>
    <edition/>
    <issue>21</issue>
    <volume/>
    <type>article</type>
    <publisherName>Royal Society of Chemistry</publisherName>
    <publisherPlace>Cambridge</publisherPlace>
    <creatingCorporation>Chemical Society</creatingCorporation>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Sensory hybrid host materials for the selective chromo-fluorogenic detection of biogenic amines</title>
    <parentTitle language="eng">Chemical communications</parentTitle>
    <identifier type="old">14292</identifier>
    <identifier type="issn">0022-4936</identifier>
    <identifier type="issn">0009-241x</identifier>
    <identifier type="issn">1359-7345</identifier>
    <identifier type="issn">1364-548x</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">17.07.2006</enrichment>
    <author>B. García-Acosta</author>
    <author>M. Comes</author>
    <author>J.L. Bricks</author>
    <author>M.A. Kudinova</author>
    <author>V.V. Kurdyukov</author>
    <author>A.I. Tolmachev</author>
    <author>Ana Belén Descalzo López</author>
    <author>M. Dolores Marcos</author>
    <author>Ramon Martínez-Mánez</author>
    <author>A. Moreno</author>
    <author>F. Sancenón</author>
    <author>J. Soto</author>
    <author>L.A. Villaescusa</author>
    <author>Knut Rurack</author>
    <author>J. M. Barat</author>
    <author>I. Escriche</author>
    <author>P. Amorós</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Biogene Amine</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Histamin</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Farbreaktion</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Pyralium-Farbstoffe</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Fluoreszenz</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Hybrid-Materialien</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
  <doc>
    <id>27741</id>
    <completedYear/>
    <publishedYear>2013</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>1377</pageFirst>
    <pageLast>1389</pageLast>
    <pageNumber/>
    <edition/>
    <issue>4</issue>
    <volume>78</volume>
    <type>article</type>
    <publisherName>American Chemical Society</publisherName>
    <publisherPlace>Washington, DC</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Synthesis, spectroscopic, and analyte-responsive behavior of a polymerizable naphthalimide-based carboxylate probe and molecularly imprinted polymers prepared thereof</title>
    <abstract language="eng">A naphthalimide-based fluorescent indicator monomer 1 for the integration into chromo- and fluorogenic molecularly imprinted polymers (MIPs) was synthesized and characterized. The monomer was equipped with a urea binding site to respond to carboxylate-containing guests with absorption and fluorescence changes, namely a bathochromic shift in absorption and fluorescence quenching. Detailed spectroscopic analyses of the title compound and various models revealed the signaling mechanism. Titration studies employing benzoate and Z-ʟ-phenylalanine (Z-ʟ-Phe) suggest that indicator monomers such as the title compound undergo a mixture of deprotonation and complex formation in the presence of benzoate but yield hydrogen-bonded complexes, which are desirable for the molecular imprinting process, with weakly basic guests like Z-ʟ-Phe. Compound 1 could be successfully employed in the synthesis of monolithic and thin-film MIPs against Z-ʟ-Phe, Z-L-glutamic acid, and penicillin G. Chromatographic assessment of the selectivity features of the monoliths revealed enantioselective discrimination and clear imprinting effects. Immobilized on glass coverslips, the thin-film MIPs of 1 displayed a clear signaling behavior with a pronounced enantioselective fluorescence quenching dependence and a promising discrimination against cross-analytes.</abstract>
    <parentTitle language="eng">The journal of organic chemistry</parentTitle>
    <identifier type="old">30575</identifier>
    <identifier type="doi">10.1021/jo3019522</identifier>
    <identifier type="issn">0022-3263</identifier>
    <identifier type="issn">1520-6904</identifier>
    <enrichment key="date_peer_review">25.02.2013</enrichment>
    <author>R. Wagner</author>
    <author>Wei Wan</author>
    <author>Mustafa Biyikal</author>
    <author>E. Benito-Pena</author>
    <author>M.C. Moreno-Bondi</author>
    <author>I. Lazraq</author>
    <author>Knut Rurack</author>
    <author>B. Sellergren</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Aminosäuren</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Enantioselektivität</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Fluoreszenz</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Molekular geprägte polymere</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Sensorfilme</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
  </doc>
</export-example>
