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      <dc:title>Extended Alkenyl and Alkynyl Benzotriazoles with enhanced Two‐Photon Absorption properties as a promising alternative to Benzothiadiazoles</dc:title>
      <dc:creator>Torres-Moya, Ivan</dc:creator>
      <dc:creator>Benítez-Martín, Carlos</dc:creator>
      <dc:creator>Donoso, Beatriz</dc:creator>
      <dc:creator>Tardio, Carlos</dc:creator>
      <dc:creator>Martin, Raul</dc:creator>
      <dc:creator>Carrillo, Jose Ramon</dc:creator>
      <dc:creator>Diaz-Ortiz, Angel</dc:creator>
      <dc:creator>Nájera-Albendín, Francisco</dc:creator>
      <dc:creator>Prieto, Pilar</dc:creator>
      <dc:creator>Perez-Inestrosa, Ezequiel</dc:creator>
      <dc:subject>Fluorescencia</dc:subject>
      <dc:description>A series of donor–p–acceptor–p–donor (D-p-A-p-D) benzoazole dyes with 2H-benzo[d][1,2,3]triazole or BTDcores have been prepared and their photophysical proper-ties characterized. The properties of these compounds dis-play remarkable differences, mainly as a result of the elec-tron-donor substituent. Dyes with the best properties havevisible-light absorption over l = 400 nm, large Stokes shiftsin the range of about 3500–6400 cm@1, and good fluores-cence emission with quantum yields of up to 0.78. The two-photon absorption properties were also studied to establishthe relationship between structure and properties in the dif-ferent compounds synthesized. These results provided crosssections of up to 1500 GM, with a predominance of S2! S0transitions and a high charge-transfer character. Time-depen-dent DFT calculations supported the experimental results.</dc:description>
      <dc:date>2025-01-10T08:33:15Z</dc:date>
      <dc:date>2025-01-10T08:33:15Z</dc:date>
      <dc:date>2019</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>I. Torres-Moya, C. Benitez-Martin, B. Donoso, C. Tardío, R. Martín, J. R. Carrillo, Á. Díaz-Ortiz, F. Najera, P. Prieto, E. Perez-Inestrosa, Extended Alkenyl and Alkynyl Benzotriazoles with enhanced Two‐Photon Absorption properties as a promising alternative to Benzothiadiazoles.  Chem. Eur. J. 2019, 25, 15572</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/36107</dc:identifier>
      <dc:identifier>10.1002/chem.201903493</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>open access</dc:rights>
      <dc:publisher>Wiley-VCH Verlag GmbH &amp; Co</dc:publisher>
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