Nitrated aromatic molecules have unique photoinduced channels. Due to the presence of
oxygen-centered non-bonding orbitals, they can undergo sub-picosecond intersystem …

Electron-deficient π-conjugated functional dyes lie at the heart of organic optoelectronics.
Adding nitro groups to aromatic compounds usually quenches their fluorescence via inter …

Nitroaromatics seldom fluoresce. The importance of electron-deficient (n-type) conjugates,
however, has inspired a number of strategies for suppressing the emission-quenching …

Femtosecond transient absorption experiments and density functional calculations are
presented for 2-methyl-1-nitronaphthalene, 2-nitronaphthalene, and 1-nitronaphthalene in …

Nitrated polycyclic molecules can present the largest singlet–triplet crossing rates among
organic molecules. This implies that most of these compounds have no detectable steady …

Nitrobenzene is the simplest nitroaromatic compound and yet is characterized by a
challenging and rich photophysics and photochemistry. In the present contribution, the main …

The importance of electrochemical analysis for charge-transfer science cannot be
overstated. Interfaces in electrochemical cells present certain challenges in the …

The photophysics of most nitrated polycyclic aromatic compounds is dominated by an
ultrafast intersystem crossing channel, which makes their first singlet excited states decay …

The photochemistry of nitro-substituted polyaromatic compounds is generally determined by
the rapid decay of its S1 state and the rapid population of its triplet manifold. Previous …

Nitronaphthalene derivatives (NNDs) are among the most abundant volatile nitro-polycyclic
aromatic hydrocarbons found in the Earth's atmosphere. Investigations of the atmospheric …