<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>30443</id>
    <completedYear/>
    <publishedYear>2013</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>17</pageFirst>
    <pageLast>20</pageLast>
    <pageNumber/>
    <edition/>
    <issue>1</issue>
    <volume>2</volume>
    <type>article</type>
    <publisherName>Wiley-VCH-Verl.</publisherName>
    <publisherPlace>Weinheim</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Carbon dioxide adsorption in Betulin-based micro- and macroporous polyurethanes</title>
    <abstract language="eng">Separation of CO2. Microporous polyurethane networks were prepared based on a renewable resource. Betulin, extracted from birch bark, is used as a structure-directing diol monomer in A3-B2 monomers. The resulting microporous networks show very promising CO2/N2 selectivities. The state of adsorbed CO2 is analyzed by in situ NMR spectroscopy, and pure physisorption is proven. The preparation of monolithic materials is demonstrated as well.</abstract>
    <parentTitle language="eng">ChemistryOpen</parentTitle>
    <identifier type="old">33416</identifier>
    <identifier type="doi">10.1002/open.201200045</identifier>
    <identifier type="issn">2191-1363</identifier>
    <identifier type="urn">urn:nbn:de:kobv:b43-304431</identifier>
    <enrichment key="date_peer_review">27.03.2014</enrichment>
    <licence>Creative Commons - CC BY-NC - Namensnennung - Nicht kommerziell 4.0 International</licence>
    <author>J. Jeromenok</author>
    <author>W. Böhlmann</author>
    <author>Christian Jäger</author>
    <author>J. Weber</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Carbon dioxide</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Gas adsorption</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Microporous polymers</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Renewable resources</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Solid state NMR spectroscopy</value>
    </subject>
    <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/30443/Jeromenok_et_al-2013-ChemistryOpen.pdf</file>
  </doc>
  <doc>
    <id>27725</id>
    <completedYear/>
    <publishedYear>2012</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>11630</pageFirst>
    <pageLast>11640</pageLast>
    <pageNumber/>
    <edition/>
    <issue>37</issue>
    <volume>18</volume>
    <type>article</type>
    <publisherName>Wiley-VCH Verl.</publisherName>
    <publisherPlace>Weinheim</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">An isoreticular family of microporous metal-organic frameworks based on zinc and 2-substituted imidazolate-4-amide-5-imidate: syntheses, structures and properties</title>
    <abstract language="eng">We report on a new series of isoreticular frameworks based on zinc and 2-substituted imidazolate-4-amide-5-imidate (IFP-1–4, IFP=imidazolate framework Potsdam) that form one-dimensional, microporous hexagonal channels. Varying R in the 2-substitued linker (R=Me (IFP-1), Cl (IFP-2), Br (IFP-3), Et (IFP-4)) allowed the channel diameter (4.0–1.7 Å), the polarisability and functionality of the channel walls to be tuned. Frameworks IFP-2, IFP-3 and IFP-4 are isostructural to previously reported IFP-1. The structures of IFP-2 and IFP-3 were solved by X-ray crystallographic analyses. The structure of IFP-4 was determined by a combination of PXRD and structure modelling and was confirmed by IR spectroscopy and 1H MAS and 13C CP-MAS NMR spectroscopy. All IFPs showed high thermal stability (345–400°C); IFP-1 and IFP-4 were stable in boiling water for 7 d. A detailed porosity analysis was performed on the basis of adsorption measurements by using various gases. The potential of the materials to undergo specific interactions with CO2 was investigated by measuring the isosteric heats of adsorption. The capacity to adsorb CH4 (at 298 K), CO2 (at 298 K) and H2 (at 77 K) at high pressure were also investigated. In situ IR spectroscopy showed that CO2 is physisorbed on IFP-1–4 under dry conditions and that both CO2 and H2O are physisorbed on IFP-1 under moist conditions.</abstract>
    <parentTitle language="eng">Chemistry - A European journal</parentTitle>
    <identifier type="old">30559</identifier>
    <identifier type="doi">10.1002/chem.201200889</identifier>
    <identifier type="issn">0947-6539</identifier>
    <identifier type="issn">1521-3765</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">21.02.2013</enrichment>
    <author>F. Debatin</author>
    <author>K. Behrens</author>
    <author>J. Weber</author>
    <author>I. A. Baburin</author>
    <author>A. Thomas</author>
    <author>J. Schmidt</author>
    <author>I. Senkovska</author>
    <author>S. Kaskel</author>
    <author>A. Kelling</author>
    <author>N. Hedin</author>
    <author>Z. Bacsik</author>
    <author>S. Leoni</author>
    <author>G. Seifert</author>
    <author>Christian Jäger</author>
    <author>C. Günter</author>
    <author>U. Schilde</author>
    <author>A. Friedrich</author>
    <author>H.-J. Holdt</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Adsorption</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Metal-organic frameworks</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Microporous materials</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>N,O ligands</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Zinc</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>29813</id>
    <completedYear/>
    <publishedYear>2014</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>430</pageFirst>
    <pageLast>432</pageLast>
    <pageNumber/>
    <edition/>
    <issue>4</issue>
    <volume>50</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">From dense monomer salt crystals to CO2 selective microporous polyimides via solid-state polymerization</title>
    <abstract language="eng">Fully aromatic polyimides are synthesized via solid-state polymerization of the corresponding monomer salts. The crystal structure of salts shows strong hydrogen bonding of the reactive groups and thereby paves the way for solid-state transformations. The polycondensation yields copies of the initial salt crystallite habits, accompanied by the development of a porosity especially suited for CO2.</abstract>
    <parentTitle language="eng">Chemical communications</parentTitle>
    <identifier type="old">32747</identifier>
    <identifier type="doi">10.1039/c3cc47674j</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="date_peer_review">06.01.2014</enrichment>
    <author>M.M. Unterlass</author>
    <author>Franziska Emmerling</author>
    <author>M. Antonietti</author>
    <author>J. Weber</author>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Datei im Netzwerk der BAM verfügbar ("Closed Access")</collection>
  </doc>
</export-example>
