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Volumn 102, Issue 9, 1980, Pages 3163-3173

Diels-Alder Reactivity of Polycyclic Aromatic Hydrocarbons. 1. Acenes and Benzologs

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EID: 0040963619     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00529a046     Document Type: Article
Times cited : (224)

References (45)
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    • Except for a slight intensification of the α bands, a broadening of the vibrational components, and red shift by about 10 nm due to the newly formed sp3 carbon atoms
    • Except for a slight intensification of the α bands, a broadening of the vibrational components, and red shift by about 10 nm due to the newly formed sp3 carbon atoms, the UV spectra of the adducts resemble those of the remaining chromophores.
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    • Int. Ed. Engl., 3, 617. The EA of maleic anhydride reported here was deduced from charge-transfer spectra; no electron transmission data are yet available.
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    • Note that positive EAs correspond to bound states, i.e., to negative orbital energies.
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    • to be published. For earlier attempts to calculate 7r IPs using Huckel theory see ref 23 and P. A. Clark, F. Brogli, and E. Heilbronner
    • P. Eilfeld and W. Schmidt, to be published. For earlier attempts to calculate 7r IPs using Huckel theory see ref 23 and P. A. Clark, F. Brogli, and E. Heilbronner, Heiv. Chim. Acta, 55, 1415 (1972).
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    • For example, 13, 751 (1974); A. Graovac, I. Gutman, and N. Trinajstic, “Topological Approach to the Chemistry of Conjugated Molecules ‘, Springer-Verlag, West Berlin, p
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