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Updated: Jul 16, 2025

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Realization of nitroaromatic chromophores with intense two-photon brightness
Bartłomiej Sadowski1, Marzena Kaliszewska2, Guillaume Clermont3
1Centre of New Technologies, University of Warsaw, S. Banacha 2c, Warsaw 02-097, Poland. b.sadowski@cent.uw.edu.pl.
Abstract:
Strong fluorescence is a general feature of dipyrrolonaphthyridinediones bearing two nitrophenyl substituents. Methyl groups simultaneously being weakly electron-donating and inducing steric hindrance appear to be a key structural parameter that allows for significant emission enhancement, whereas Et2N groups cause fluorescence quenching. The magnitude of two-photon absorption increases if 4-nitrophenyl substituents are present while the contribution of Et2N groups is detrimental.
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