<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>Mareda J</dc:creator>
  <dc:creator>Matile S</dc:creator>
  <dc:date>2009</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The recognition and transport of anions is usually accomplished by hydrogen bonding, ion pairing, metal coordination, and anion-dipole interactions. Here, we elaborate on the concept to use anion-pi interactions for this purpose. Different to the popular cation-pi interactions, applications of the complementary pi-acidic surfaces do not exist. This is understandable because the inversion of the aromatic quadrupole moment to produce pi-acidity is a rare phenomenon. Here, we suggest that pi-acidic aromatics can be linked together to produce an unbendable scaffold with multiple binding sites for anions to move along across a lipid bilayer membrane. The alignment of multiple anion-pi sites is needed to introduce a cooperative multi-ion hopping mechanism. Experimental support for the validity of the concept comes from preliminary results with oligonaphthalenediimide (O-NDI) rods. Predicted by strongly positive facial quadrupole moments, the cooperativity and chloride selectivity found for anion transport by O-NDI rods were consistent with the existence of anion-pi slides. The proposed mechanism for anion transport is supported by DFT results for model systems, as well as MD simulations of rigid O-NDI rods. Applicability of anion-pi slides to achieve electroneutral photosynthesis is elaborated with the readily colorizable oligoperylenediimide (O-PDI) rods. To clarify validity, scope and limitations of these concepts, a collaborative research effort will be needed to address by computer modeling and experimental observations the basic questions in simple model systems and to design advanced multifunctional anion-pi architectures.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/191790</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.200801643</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/19035366</dc:relation>
  <dc:source>Chemistry (Weinheim an der Bergstrasse, Germany). - 2009</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Anions</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Binding Sites</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Biological Transport</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Cations</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Hydrogen Bonding</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Lipid Bilayers</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Metals</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Models, Chemical</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Models, Molecular</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Naphthalenes</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Photochemistry</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Static Electricity</dc:subject>
  <dc:title xmlns:ns13="xml" ns13:lang="en">Anion-pi slides for transmembrane transport.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
