<?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>2026-04-27T01:59:25Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18354" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18354</identifier><datestamp>2024-11-28T15:10:28Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Gámez-Valenzuela, Sergio</subfield>
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      <subfield code="a">Neusser, David</subfield>
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      <subfield code="a">Benitez-Martín, Carlos</subfield>
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      <subfield code="a">Najera, Francisco</subfield>
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      <subfield code="a">Guadix, Juan A.</subfield>
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      <subfield code="a">Moreno-Yruela, Carlos</subfield>
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      <subfield code="a">Villacampa, Belén</subfield>
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      <subfield code="a">Ponce Ortíz, Rocío</subfield>
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      <subfield code="a">Ludwigs, Sabine</subfield>
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      <subfield code="a">Andreu, Raquel</subfield>
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      <subfield code="a">Ruiz Delgado, M. Carmen</subfield>
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      <subfield code="c">2021-05-25</subfield>
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      <subfield code="a">We report the synthesis and comprehensive study of two chromophores based on 4H-pyranylidene moiety as a part of the π-conjugated spacer. Triphenylamine (TPA) acts as donor and tricarbonitrile-based electron-accepting groups complete these V-shaped D–A–D architectures (A, acceptor; D, donor). Their electrochemical, photophysical and nonlinear optical properties are analyzed in detail by using a joint experimental and theoretical approach. The two chromophores exhibit near-infrared fluorescence, large Stokes shift, enhanced emission in tetrahydrofuran/water mixtures and good photostability. Additionally, the dimerization of triphenylamine groups to tetraphenylbenzidine (TPB) takes place upon electrochemical and chemical oxidation showing their peculiar electrochemical behavior and film formation capabilities. Interestingly, high molecular first hyperpolarizabilities and two-photon absorption cross-sections were found, highlighting their potential applications in electro-optical devices. Overall, our work demonstrates that these near-infrared (NIR) fluorescent chromophores are versatile materials with a myriad of applications ranging from optoelectronics to biological applications.</subfield>
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      <subfield code="a">http://hdl.handle.net/10668/4531</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/18354</subfield>
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      <subfield code="a">10.1039/D1MA00415H</subfield>
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      <subfield code="a">2633-5409</subfield>
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      <subfield code="a">Material Advances</subfield>
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      <subfield code="a">Fluorescence</subfield>
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      <subfield code="a">Electrons</subfield>
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      <subfield code="a">Dimerization</subfield>
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      <subfield code="a">Tetrahydrofuran</subfield>
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      <subfield code="a">Chromophore-Assisted Light Inactivation</subfield>
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      <subfield code="a">Chemical oxidation</subfield>
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      <subfield code="a">Fluorescencia</subfield>
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      <subfield code="a">Electrones</subfield>
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      <subfield code="a">Dimerización</subfield>
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      <subfield code="a">4-Butirolactona</subfield>
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      <subfield code="a">Inactivación por luz asistida por cromóforos</subfield>
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      <subfield code="a">V-shaped pyranylidene/triphenylamine-based chromophores with enhanced photophysical, electrochemical and nonlinear optical properties</subfield>
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