The electronic structures of 206 carbonyls and methylene derivatives based on conjugated cyclic hydrocarbons are computationally studied in this work using theoretical methods of quantum chemistry. The singlet open-shell nature of the ground state and its influence on the low-lying excited states is analyzed for 90 carbonyl (quinone, Q), 90 methylene (quinone dimethide, QDM) and 26 carbonyl-methylene (quinone methide, QM) mixed derivatives in the pursuit of new promising candidates for singlet fission sensitizers. Non-negligible diradical character is observed for most of the studied molecules, which is mainly determined by the nature and the relative position of the substituting groups in the bare rings. In general, the methylene group enhances to a greater extent the diradical character and the following trend is observed: y(QDM) > y(QM) > y(Q). This feature leads to a decrease in the energy of the S → S and, especially, the S → T transitions, facilitating the accomplishment of the singlet fission energetic conditions: 2T-S ≤ 0 (C1) and 2T-T < 0 (C2). For all the methylene derivatives, these transitions have π → π* character, while some carbonyl-containing molecules, in particular those with low diradical character, show transitions with n → π* character, due to the presence of the lone pairs of the oxygen atom. From the total set of 206 molecules analyzed, 10 molecules with intermediate diradical character may be considered as potential candidates to undergo singlet fission efficiently.

The ability of different carbon allotropes surfaces as potential substrates for enhanced Raman spectroscopy is analysed theoretically and the factors responsible of the Raman-enhancing mechanism deeply scrutinised. Our analysis is based on the partition of the Raman tensor into molecule and surface terms, which leads to three different contributions to the Raman activity ('molecule', 'surface' and 'intermolecular'). Both static and pre-resonance conditions are considered in our analysis of the Raman spectra of pyridine adsorbed on model planar and curved surfaces and the three contributions to the Raman activity obtained separately. At static conditions, there is a general decrease in the Raman activity of vibrational modes associated to the molecule, proportional to the strength of the molecule-surface interaction. This stems from a reduction of the polarizability of pyridine upon its adsorption on the carbon surface. Under pre-resonance conditions, the surface contributes significantly to the Raman activity of the pyridine vibrational modes, even if the electronic transition involves exclusively energy levels from the surface. This is because of small vibrational couplings between molecular and surface modes which are negligible in metallic surface-like silver. It suggests also the possibility of finding similar effects in metallic surface built from lighter atoms like silicon or aluminium.

Small nanographene structures are promising for the development of SERS platforms at the frontier of nanometer and subnanometer scales.

Quantum chemistry is employed to estimate the effects that the structural modification of 1,5- and 9,10-anthraquinones produces in their electronic structure, in the pursuit of a common strategy to improve the electrochemical and singlet fission features on conjugated quinones.

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