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Intramolecular hetero-dimer radical cation of naphthalene-phenanthrene and naphthalene-pyrene chromophores formation

✍ Scribed by Akira Tsuchida; Hiroshi Takamura; Masahide Yamamoto


Book ID
103034307
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
308 KB
Volume
198
Category
Article
ISSN
0009-2614

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✦ Synopsis


The formation of the intramolecular naphthalene-phenanthrene hetero-dimer radical cation was observed by nanosecond laser photolysis in the visible and near-IR regions. A charge resonance band was observed at 1450 nm in acetonitrile at 298 K. The intramolecular naphthalene-pyrene hetero-dimer radical cation, however, could not be observed at room temperature due to the small stabilization energy of charge resonance. The ionization potentials of both constituent chromophores must be nearly equal for the hetero-dimer radical cation to be sufficiently stable.


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✍ C. Niederalt; S. Grimme; S.D. Peyerimhoff πŸ“‚ Article πŸ“… 1995 πŸ› Elsevier Science 🌐 English βš– 586 KB

Ab initio calculations for the excited states of the positive ions of naphthalene, anthracene and phenanthrene have been carried out to elucidate their absorption spectra in the UV-VIS range (200-1000 nm). With restricted open-shel! Hartree-Fock one-particle basis functions employing double-~" or tr