Ultrafast processes triggered by one- and two-photon excitation of a photochromic and luminescent hydrazone

  1. Alessandro Iagatti,
  2. Baihao Shao,
  3. Alberto Credi,
  4. Barbara Ventura ,
  5. Ivan Aprahamian and
  6. Mariangela Di Donato ORCID Logo

Submitting author affiliation: ISOF-CNR, Bologna, Italy

Beilstein Arch. 2019, 201948. doi:10.3762/bxiv.2019.48.v1

Published 27 Jun 2019

  • Preprint

Abstract

In this work we apply a combination of steady state and time resolved luminescence and absorption spectroscopies to investigate the excited-state dynamics of a recently developed molecular photoswitch, belonging to the hydrazone family. The outstanding properties of this molecule, involving fluorescence toggling, bistability, high isomerization quantum yield and non-negligible two-photon absorption cross section, make it very promising for numerous applications. Here we show that the light induced Z/E isomerization occurs on a fast <1 ps timescale in both toluene and acetonitrile, while the excited state lifetime decreases with increasing solvent polarity, suggesting a partial charge transfer nature of its low lying excited state. Time resolved luminescence measurements evidence the presence of a main emission component in the 500-520 nm spectral range, attributed to the Z isomer, and a very short living blue-shifted emission, attributed to the E isomer. Finally, transient absorption measurements performed upon far-red excitation are employed as an alternative method to determine the two-photon absorption cross-section of the molecule.

Keywords: Hydrazone, pump-probe spectroscopy, time resolved fluorescence

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When a peer-reviewed version of this preprint is available in the Beilstein Journals, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:

Iagatti, A.; Shao, B.; Credi, A.; Ventura, B.; Aprahamian, I.; Di Donato, M. Beilstein Arch. 2019, 201948. doi:10.3762/bxiv.2019.48.v1

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