Publication | Closed Access
Effect of protonation on the electronic structure of aromatic molecules: naphthaleneH+
68
Citations
32
References
2010
Year
Organic Charge-transfer CompoundEngineeringNeutral Naphthalene CounterpartBiochemistryNatural SciencesSpectroscopyLarge Red ShiftAromatic MoleculesProton TransferProton-coupled Electron TransferOrganic ChemistryPhysical ChemistryQuantum ChemistryChemistryElectronic StructurePolycyclic Aromatic HydrocarbonBiophysics
Protonated naphthalene, the smallest protonated polycyclic aromatic hydrocarbon cation, absorbs in the visible, around 500 nm, which corresponds to an unusually large red shift with respect to the neutral naphthalene counterpart.
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