Theoretical and Experimental Study on Boron β‐Diketonate Complexes with Intense Two‐Photon‐Induced Fluorescence in Solution and in the Solid State |
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Authors: | Dr Pierre‐Henri Lanoë Dr Bastien Mettra Dr Yuan Yuan Liao Dr Nathalie Calin Dr Anthony D'Aléo Tomotaka Namikawa Prof Kenji Kamada Prof Fréderic Fages Dr Cyrille Monnereau Dr Chantal Andraud |
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Institution: | 1. Laboratoire de Chimie UMR CNRS 5182, Ecole Normale Supérieure de Lyon/Université de Lyon, 46, Lyon, France;2. CINAM UMR CNRS 7325, Université Aix-Marseille, Marseille, France;3. IFMRI, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka 563-8577, Japan |
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Abstract: | Three boron diketonate chromophores with extended π‐conjugated backbone were prepared and their spectroscopic features were investigated through a combined theoretical/experimental study. It was shown that these complexes, which undergo very large electronic reorganization upon photoexcitation, combine large two‐photon absorption cross section with an emission energy and quantum efficiency in solution that is strongly dependent on solvent polarity. The strong positive influence of boron complexation on the magnitude of the two‐photon absorption was clearly established, and it was shown that the two‐photon absorption properties were dominated by the quadrupolar term. For one of the synthesized compounds, intense one‐ and two‐photon‐induced solid‐state emission (fluorescence quantum yield of 0.65 with maximum wavelength of 610 nm) was obtained as a result of antiparallel J‐aggregate crystal packing. |
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Keywords: | boron chromophores fluorescence solid-state emission theoretical calculations |
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