<?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>2026-08-22T00:38:41Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/114860" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/114860</identifier><datestamp>2025-01-18T00:54:09Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>“Push-no-pull” porphyrins for second harmonic generation imaging</dc:title>
   <dc:creator>López Duarte, Ismael</dc:creator>
   <dc:creator>Reeve, James E.</dc:creator>
   <dc:creator>Pérez-Moreno, Javier</dc:creator>
   <dc:creator>Boczarow, Igor</dc:creator>
   <dc:creator>Depotter, Griet</dc:creator>
   <dc:creator>Fleischhauer, Jan</dc:creator>
   <dc:creator>Clays, Koen</dc:creator>
   <dc:creator>Anderson, Harry L.</dc:creator>
   <dc:subject>615:54</dc:subject>
   <dc:subject>615.31</dc:subject>
   <dc:subject>Química farmaceútica</dc:subject>
   <dc:subject>23 Química</dc:subject>
   <dc:description>The established approach to design a molecule with strong second-order nonlinear optical (NLO) activity is to connect an electron-donor to an electron-acceptor via a pi-conjugated bridge, to generate push-pull system. Surprisingly, we have found that dyes with large first hyperpolarizabilities, and which exhibit strong second harmonic generation (SHG), can be created just by attaching an electron-donor to a porphyrin. The free-base porphyrin core is sufficiently electron-deficient that the hyperpolarizability does not increase on addition of a pyridinium electron-acceptor.</dc:description>
   <dc:description>Deutsche Forschungsgemeinscha</dc:description>
   <dc:description>European Commission</dc:description>
   <dc:description>Depto. de Química en Ciencias Farmacéuticas</dc:description>
   <dc:description>Fac. de Farmacia</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2025-01-17T10:06:44Z</dc:date>
   <dc:date>2025-01-17T10:06:44Z</dc:date>
   <dc:date>2013</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/114860</dc:identifier>
   <dc:identifier>2041-6520</dc:identifier>
   <dc:identifier>2041-6539</dc:identifier>
   <dc:identifier>10.1039/c3sc22306j</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>PIEF-GA2009-255164</dc:relation>
   <dc:relation>López-Duarte I, Reeve JE, Pérez-Moreno J, Boczarow I, Depotter G, Fleischhauer J, et al. “Push-no-pull” porphyrins for second harmonic generation imaging. Chem Sci [Internet]. 2013 [citado 17 de enero de 2025];4(5):2024. Disponible en: https://xlink.rsc.org/?DOI=c3sc22306j</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>restricted access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Royal Society of Chemistry</dc:publisher>
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