15min:

MOHAMMED BAHOU, Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, Hsinchu 30010, Taiwan; YU-JONG WU, National Synchrotron Radiation Research Center, 101 Hsin-Ann Road, Hsinchu Science Park, Hsinchu 30076, Taiwan; YUAN-PERN LEE, Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, Hsinchu 30010, Taiwan and Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 10617, Taiwan.

We report the infrared (IR) spectra of protonated naphthalene (C₁₀H₉⁺) and hydronaphthyl radical (C₁₀H₉) in both - and -forms trapped in solid para-hydrogen (p-H₂). These species were produced on electron bombardment of a mixture of p-H₂ and naphthalene during deposition. The IR features of -C₁₀H₉⁺ were identified on observing the decay of IR lines, whereas those of -C₁₀H₉ and -C₁₀H₉ were identified with the increased intensity after the matrix sample was maintained in darkness for an extended period. IR features of -C₁₀H₉ and -C₁₀H₉ were further characterized on irradiation of a matrix sample with UV or visible light. Irradiation of the matrix sample with visible light (495-700 nm) generated neutral C₁₀H₉ in both forms, whereas irradiation with light at 365 nm generated only -C₁₀H₉. Lines due to -C₁₀H₉⁺ were observed only during the initial period of acquisition of an IR spectrum after secondary photolysis of the matrix sample. Observed wavenumbers and relative intensities agree satisfactorily with the anharmonic vibrational wavenumbers and IR intensities predicted for these species with the B3LYP/6-311++G(2d,2p) method. Compared with literature spectra recorded previously with IR photodissociation of Ar-tagged compounds or IR multiphoton dissociation,\footnote U.~J.~Lorenz, N.~Solcá, J.~Lemaire, P.~Maître and O.~Dopfer, Angew. Chem. Int. Ed, \underline\textbf46, 6714 (2007). our method has the advantages of producing IR spectra with high resolution, true intensity and wide spectral coverage for both protonated polycyclic aromatic hydrocarbons and their neutral counterparts with little interference from other fragments. With these advantages, the IR spectra of -C₁₀H₉⁺ and -C₁₀H₉⁺ were clearly distinguished.