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               <dc:title>Controlling Two-Photon Action Cross Section by Changing a Single Heteroatom Position in Fluorescent Dyes</dc:title>
               <dc:creator>Ośmiałowski, Borys</dc:creator>
               <dc:creator>Petrusevich, Elizaveta F.</dc:creator>
               <dc:creator>Antoniak, Magda A.</dc:creator>
               <dc:creator>Grela, Izabela</dc:creator>
               <dc:creator>Bin Jassar, Mohammed A.</dc:creator>
               <dc:creator>Nyk, Marcin</dc:creator>
               <dc:creator>Luis Luis, Josep Maria</dc:creator>
               <dc:creator>Jędrzejewska, Beata</dc:creator>
               <dc:creator>Zaleśny, Robert</dc:creator>
               <dc:creator>Jacquemin, Denis</dc:creator>
               <dc:subject>Fotons</dc:subject>
               <dc:subject>Photons</dc:subject>
               <dc:subject>Fisicoquímica</dc:subject>
               <dc:subject>Chemistry, Physical and theoretical</dc:subject>
               <dc:description>The optimization of nonlinear optical properties for “real-life” applications remains a key challenge for both experimental and theoretical approaches. In particular, for two-photon processes, maximizing the two-photon action cross section (TPACS), the figure of merit for two-photon bioimaging spectroscopy, requires simultaneously controlling all its components. In the present Letter, a series of difluoroborates presenting various heterocyclic rings as an electron acceptor have been synthesized and their absorption, fluorescence, photoisomerization, and two-photon absorption features have been analyzed using both experimental and theoretical approaches. Our results demonstrate that the TPACS values can be fine-tuned by changing the position of a single heteroatom, which alters the fluorescence quantum yields without changing the intrinsic two-photon absorption cross section. This approach offers a new strategy for optimizing TPACS</dc:description>
               <dc:description>J.M.L. is grateful for financial support from the Spanish MICIN PGC2018-098212-B-C22 and the Catalan DIUE 2017SGR39</dc:description>
               <dc:date>2024-06-18T13:55:42Z</dc:date>
               <dc:date>2024-06-18T13:55:42Z</dc:date>
               <dc:date>2020-07-06</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:type>peer-reviewed</dc:type>
               <dc:identifier>http://hdl.handle.net/10256/18454</dc:identifier>
               <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpclett.0c01438</dc:relation>
               <dc:relation>info:eu-repo/semantics/altIdentifier/issn/1948-7185</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-098212-B-C22/ES/DESCOMPOSICION EN EL ESPACIO REAL DE PROPIEDADES OPTICAS NO LINEALES PARA EL DISEÑO RACIONAL DE MATERIALES OPTOELECTRONICOS/</dc:relation>
               <dc:rights>Attribution 4.0 International</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>American Chemical Society (ACS)</dc:publisher>
               <dc:source>Journal of Physical Chemistry Letters, 2020, vol. 11, núm. 15, p. 5920–5925</dc:source>
               <dc:source>Articles publicats (D-Q)</dc:source>
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