<?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>2026-05-28T14:25:12Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/14080" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/14080</identifier><datestamp>2026-02-03T12:09:56Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Two-Photon Fluorescence As Tool For Imaging In Cells</dc:title>
   <dc:creator>Collado-Martín, Daniel</dc:creator>
   <dc:subject>Flúor -- Efectos fisiológicos</dc:subject>
   <dcterms:abstract>Fluorescent probes are essential tools for studying biological systems. The last decade has witnessed particular interest in the development of two-photon excitable probes, due to their advantageous features in tissue imaging compared to one-photon probes [1]. Recently, we have designed and synthesized an aminonaphthalimide–BODIPY derivative as energy transfer cassette which was found to show very fast and efficient BODIPY fluorescence sensitization [2]. This was observed upon one- and two-photon excitation, which extends the application range of the investigated bichromophoric dyads in terms of accessible excitation wavelengths. In order to increase the two-photon absorption of the system the aminonaphthalimide fluorophore was replaced with a Prodan analogue, which presents a variety of applications as probes and labels in biology [3]. The two-photon absorption cross-section  of the dyads is significantly incremented by the presence of the 6-acetyl-2-naphthylamine donor group. &#xd;
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We also explore in this communication the use of new fluorophores based on four-coordinate organoboron N,C-chelates containing an arylisoquinoline skeleton in confocal fluorescence microscopy that show significant two-photon absorption cross sections and allow the use of excitation wavelengths in the near-infrared region [4].References&#xd;
[1] H. M. Kim, B. R. Cho, Chem. Rev. 2015, 5014–5055. &#xd;
[2] D. Collado, P. Remón, Y. Vida, F. Nájera, P. Sen, U. Pischel, E. Perez-Inestrosa, Chem. Asian J. 2014, 9, 797–804. &#xd;
[3] O. A. Kucherak, P. Didier, Y. Mely, A. S. Klymchenko, J. Phys. Chem. Lett. 2010, 1, 616–620.&#xd;
[4] V. F. Pais, M. M. Alcaide, R. López-Rodriguez, D. Collado, F. Nájera,  E. Perez-Inestrosa, E. Álvarez, J. M. Lassaletta, R. Fernández, A. Ros, U. Pischel, Chem. Eur. J. 2015, 21, 15369–15376.</dcterms:abstract>
   <dcterms:dateAccepted>2017-06-30T10:10:15Z</dcterms:dateAccepted>
   <dcterms:available>2017-06-30T10:10:15Z</dcterms:available>
   <dcterms:created>2017-06-30T10:10:15Z</dcterms:created>
   <dcterms:issued>2017-06-30</dcterms:issued>
   <dc:type>conference output</dc:type>
   <dc:identifier>http://hdl.handle.net/10630/14080</dc:identifier>
   <dc:identifier>http://orcid.org/0000-0002-8155-7112</dc:identifier>
   <dc:language>spa</dc:language>
   <dc:relation>XXXVI Reunión Bienal de la Real Sociedad Española de Química</dc:relation>
   <dc:relation>Sitges</dc:relation>
   <dc:relation>25/06/2017</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:rights>by-nc-nd</dc:rights>
</qdc:qualifieddc>
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