Affiliation:
1. 1Institut für Organische Chemie der Freien Universität Berlin
Abstract
The polarographic reduction of tetraarylcyclopentadienones is studied in connection with quantummechanical calculations basing on the well known structure of the corresponding ketyls. A linear free energy relationship is found assuming a change in conformation between the redox components. Comparison of the ketone geometry with the conformation of tetraarylpyrryls gives a prove for this surprising result.
Cited by
10 articles.
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1. Penta-arylcyclopentadienyl complexes;Coordination Chemistry Reviews;2011-08
2. Fused Supracyclopentadienyl Ligand Precursors. Synthesis, Structure, and Some Reactions of 1,3-Diphenylcyclopenta[l]phenanthrene-2-one, 1,2,3-Triphenylcyclopenta[l]phenanthrene-2-ol, 1-Chloro-1,2,3-triphenylcyclopenta[l]phenanthrene, 1-Bromo-1,2,3-triphenylcyclopenta[l]phenanthrene, and 1,2,3-Triphenyl-1H-cyclopenta[l]phenanthrene;Australian Journal of Chemistry;2006
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4. Effect of solvent polarity extremes on the coupling of cyclopropylcarbene-chromium complexes and alkynes: Synthesis of β-alkoxycyclopentadienones, 2-cyclopentene-1,3-diones, and cis 4,5-disubstituted cyclopentenones;Tetrahedron Letters;1997-01
5. Reactions of Cyclopropylcarbene-Chromium Complexes;Comments on Inorganic Chemistry;1990-04