<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Vargas Jentzsch A</dc:creator>
  <dc:creator>Matile S</dc:creator>
  <dc:date>2013</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Halogen bonds have recently been introduced as ideal to transport anions across lipid bilayer membranes. However, activities obtained with small transporters were not impressive, and cyclic arrays of strong halogen-bond donors above a calix[4]arene scaffold gave even weaker activities. Here, we report that their linear alignment for anion hopping along transmembrane rigid-rod scaffolds gives excellent activities with an unprecedented cooperativity coefficient m = 3.37.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/252283</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/ja4013276</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/23517007</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Journal of the American Chemical Society. - 2013</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Halogens</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Lipid Bilayers</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Molecular Structure</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Transmembrane halogen-bonding cascades.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
