<?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>2026-05-27T20:39:50Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/14080" metadataPrefix="mods">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><mods:mods xmlns:doc="http://www.lyncode.com/xoai" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Collado-Martín, Daniel</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2017-06-30T10:10:15Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2017-06-30T10:10:15Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2017-06-30</mods:dateIssued>
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   <mods:identifier type="uri">http://hdl.handle.net/10630/14080</mods:identifier>
   <mods:identifier type="orcid">http://orcid.org/0000-0002-8155-7112</mods:identifier>
   <mods: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.</mods:abstract>
   <mods:language>
      <mods:languageTerm>spa</mods:languageTerm>
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   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">by-nc-nd</mods:accessCondition>
   <mods:subject>
      <mods:topic>Flúor -- Efectos fisiológicos</mods:topic>
   </mods:subject>
   <mods:titleInfo>
      <mods:title>Two-Photon Fluorescence As Tool For Imaging In Cells</mods:title>
   </mods:titleInfo>
   <mods:genre>conference output</mods:genre>
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