<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-19T16:50:15Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/5707" metadataPrefix="etdms">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/5707</identifier><datestamp>2022-07-20T10:40:01Z</datestamp><setSpec>com_10259_3924</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3925</setSpec></header><metadata><thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.0/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.0/ http://www.ndltd.org/standards/metadata/etdms/1.0/etdms.xsd">
<title>Simple isophthalamides/dipicolineamides as active transmembrane anion transporters</title>
<creator>Picci, Giacomo</creator>
<creator>Carreira Barral, Israel</creator>
<creator>Alonso Carrillo, Daniel</creator>
<creator>Sanz González, David</creator>
<creator>Fernández López, Pablo</creator>
<creator>García Valverde, María</creator>
<creator>Caltagirone, Claudia</creator>
<creator>Quesada Pato, Roberto</creator>
<subject>Anion binding</subject>
<subject>anion transport</subject>
<subject>ion-selective electrode</subject>
<subject>liposomes</subject>
<description>Eight N,N´-diarylisophthalamide/dipicolineamide derivatives have been synthesised and fully characterised, both in solution and in the solid state. The transmembrane anion transport properties of these compounds have been studied by chloride-selective electrode and fluorescence experiments. The substitution pattern of the aromatic moieties determines the transport properties of these systems, with those containing electron-withdrawing groups in their structures being the most active ones of the series.</description>
<date>2021-04-14</date>
<date>2021-04-14</date>
<date>2019-12</date>
<type>info:eu-repo/semantics/article</type>
<identifier>1061-0278</identifier>
<identifier>http://hdl.handle.net/10259/5707</identifier>
<identifier>10.1080/10610278.2019.1702194</identifier>
<identifier>1029-0478</identifier>
<language>eng</language>
<relation>Supramolecular Chemistry. 2019, V. 32, n. 2, p. 112–118</relation>
<relation>https://doi.org/10.1080/10610278.2019.1702194</relation>
<relation>info:eu-repo/grantAgreement/JCyL/BU075G19</relation>
<rights>info:eu-repo/semantics/openAccess</rights>
<publisher>Taylor &amp; Francis Group</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>